YM458

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

YM458 

YM458 是一种有效的 EZH2BRD4 双重抑制剂,对 EZH2 和 BRD4 的 IC50 分别为490 nM 和 34 nM。YM458 可抑制实体癌细胞增殖和集落形成,诱导细胞周期阻滞与细胞凋亡 (apoptosis)。YM458 可用于抗癌研究。

YM458

YM458 Chemical Structure

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生物活性

YM458 is a potent EZH2 and BRD4 dual inhibitor with IC50s of 490 nM and 34 nM, respectively. YM458 inhibits cell proliferation and colony formation and induces cell cycle arrest and apoptosis in solid cancer cells. YM458 can be used for researching anticancer[1].

IC50 & Target[1]

EZH2

490 nM (IC50)

BRD4

34 nM (IC50)

体外研究
(In Vitro)

YM458 (compound D7) (0-30 μM; 6 days) has antiproliferative activities against AsPC-1 cells with an IC50 of 0.69 ± 0.16 μM; and (1 μM; 72 hours) significantly decreases the degree of H3K27me3 and c-Myc in AsPC-1[1].
YM458 (0-30 μM; 4 or 6 days) inhibits cell proliferation on a broad range of solid cancer cells, and significantly suppresses proliferation of A549 lung cancer cells and HCT116 colorectal cancer cells at 1 μM[1].
YM458 (0.05-0.4 μM; 12-20 days) inhibits colony formation of AsPC-1, HCT116, and A549 cancer cells in a dose-dependent manner[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis

Cell Line: AsPC-1[1]
Concentration: 1 μM
Incubation Time: 72 hours
Result: Decreased the degree of H3K27me3 and c-Myc significantly.

Cell Proliferation Assay

Cell Line: AsPC-1, SW1990, CFPAC-1, A549, HCC827, H1650, H292, H460, DLD1, HCT116, and RKO[1]
Concentration: 0-30 μM
Incubation Time: 4 or 6 days
Result: Inhibited cell proliferation on a broad range of solid cancer cells, and significantly suppressed proliferation of A549 lung cancer cells and HCT116 colorectal cancer cells at 1 μM.

体内研究
(In Vivo)

YM458 (60 mg/kg; IP; every other day, for 38 days) prevents tumor growth with inhibitory rates of 38.6% in AsPC-1 cells and 62.3% in A549 cells[1].
Pharmacokinetic Parameters of YM458 in Female BALB/c mice[1].

IP (80 mg/kg) PO (80 mg/kg)
t1/2 (h) 3.81 4.16
Tmax (h) 1 1
Cmax (ng/mL) 27126.3 4383.6
AUC0-24 (ng/mL·h) 273220.1 13509.1
CL (mL/min/kg) 4.88
F (%) 4.94

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: BALB/c nude mice (injected with A549 or AsPC-1)[1]
Dosage: 60 mg/kg
Administration: IP; every other day, for 38 days
Result: Prevented tumor growth with inhibitory rates of 38.6% in AsPC-1 cells and 62.3% in A549 cells.

分子量

957.62

Formula

C53H61ClN8O5S

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Guo Z, et al. Design and Synthesis of Dual EZH2/BRD4 Inhibitors to Target Solid Tumors. J Med Chem. 2022;65(9):6573-6592.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

YM281

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

YM281 

YM281 是一种有效的 EZH2 抑制剂。YM281 诱导细胞凋亡 (apoptosis) 和细胞周期停滞在 G0/G1 期。YM281 在体内显示出抗肿瘤作用。YM281 具有研究淋巴瘤的潜力。

YM281

YM281 Chemical Structure

CAS No. : 2230914-84-6

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250 mg   询价  
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生物活性

YM281 is a potent EZH2 inhibitor. YM281 induces cell apoptosis and cell cycle arrest at the G0/G1 phase. YM281 shows antitumor effects in vivo. YM281 has the potential for the research of lymphoma[1].

体外研究
(In Vitro)

YM281 (compound V2) (0-6 µM; 0-48 h) decreases the EZH2 protein level and the PRC2 (polycomb repressive complex 2) complex through the VHL (vonHippel−Lindau)-dependent ubiquitin-proteasome system[1].
YM281 (0-10 µM; 24 h) shows anticancer effects in lymphoma cells[1].
YM281 (0-5 µM) induces cell apoptosis and cell cycle arrest at the G0/G1 phase[1].
YM281 (0-5 µM; 24 h) increases the activity of caspase-3 and -7 and meanwhile reduces the cell viability in primary lymphoma cells[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: SU-DHL-2, 22Rv1 cells
Concentration: 0-6 µM
Incubation Time: 0-48 h
Result: Abrogated both the EZH2 protein level and the H3K27me3 degree in a concentration-dependent manner in 24 h, had no significant effect on the protein level of EZH1,and significantly increased the expression of EZH2 ubiquitination.

Cell Viability Assay[1]

Cell Line: SU-DHL-2, SU-DHL-4, SU-DHL-6 cells
Concentration: 0-10 µM
Incubation Time: 24 h
Result: Induced nearly complete cell viability inhibition.

Cell Cycle Analysis[1]

Cell Line: SU-DHL-6 cells
Concentration: 1, 3, 5 µM
Incubation Time: 24 h
Result: Induced cell cycle arrest at the G0/G1 phase and a profound sub-G1 population increasein a concentration-dependent manner.

Apoptosis Analysis[1]

Cell Line: SU-DHL-6 cells
Concentration: 0-5 µM
Incubation Time: 48 h
Result: Significantly increased the expression of cleaved caspase-3 and PARP.

体内研究
(In Vivo)

YM281 (80, 100 mg/kg; i.v.; 6 times for 3 weeks) shows antitumor effects and significantly reduces the expression of EZH2 protein and H3K27me3 levels[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Balb/c nude mice (SU-DHL-6 xenograft model)[1]
Dosage: 80 mg/kg
Administration: I.v.; 6 times for 3 weeks
Result: Remarkably suppressed the tumor volume and significantly reduced the EZH2 protein and H3K27me3 levels.
Animal Model: Balb/c nude mice (Jeko-1 xenograft model)[1]
Dosage: 100 mg/kg
Administration: I.v.; 6 times for 3 weeks
Result: Shows anti-tumor effects with the significantly reduced the expression of EZH2 protein and H3K27me3 levels.

分子量

1018.27

Formula

C56H71N7O9S

CAS 号

2230914-84-6

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Tu Y,et al. Design, Synthesis, and Evaluation of VHL-Based EZH2 Degraders to Enhance Therapeutic Activity against Lymphoma. J Med Chem. 2021 Jul 22;64(14):10167-10184.

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Sepantronium hydrochloride(Synonyms: YM-155 hydrochloride)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Sepantronium hydrochloride (Synonyms: YM-155 hydrochloride)

Sepantronium hydrochloride (YM-155 hydrochloride) 是一种新型 survivin 抑制剂,对 survivin 启动子的 IC50 为 0.54 nM。

Sepantronium hydrochloride(Synonyms: YM-155 hydrochloride)

Sepantronium hydrochloride Chemical Structure

CAS No. : 355406-09-6

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

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Sepantronium hydrochloride 的其他形式现货产品:

Sepantronium bromide

生物活性

Sepantronium hydrochloride (YM-155 hydrochloride) is a novel survivin suppressant with an IC50 of 0.54 nM for the inhibition of survivin promoter activity[1].

IC50 & Target

IC50: 0.54 nM (survivin)

体外研究
(In Vitro)

Sepantronium bromide (YM155; 30 μM) is not sensitive to survivn gene promoter-driven luciferase reporter activity. Sepantronium bromide shows significant supression on endogenous survivin expression in PC-3 and PPC-1 human HRPC cells with deficient p53 via transcriptional inhibition of the survivin gene promoter. Sepantronium bromide (100 nM) does not affect protein expression of c-IAP2, XIAP, Bcl-2, Bcl-xL, Bad, α-actin, and β-tubulin. Sepantronium bromide potently inhibits human cancer cell lines (mutated or truncated p53) such as PC-3, PPC-1, DU145, TSU-Pr1, 22Rv1, SK-MEL-5 and A375 with IC50s ranging from 2.3 to 11 nM, respectively[1].
Sepantronium bromide (YM155) resultin in an increase in sensitivity of NSCLC cells to γ-radiation. Sepantronium bromide combined with γ-radiation increases both the number of apoptotic cells and the activity of caspase-3. In addition, Sepantronium bromide delays the repair of radiation-induced double-strand breaks in nuclear DNA[2].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

Sepantronium bromide (YM155; 3 and 10 mg/kg) inhibits the tumor growth in PC-3 xenografts, without obvious body weight loss and blood cell count decrease. Sepantronium bromide is highly distributed to tumor tissue in vivo. Sepantronium bromide shows 80% TGI at a dose of 5 mg/kg in PC-3 orthotopic xenografts[1].
Sepantronium bromide (YM155) in combination with γ-radiation shows potent antitumor activity against H460 or Calu6 xenografts in nude mice[2].
In this orthotopic renal and metastatic lung tumors models, Sepantronium bromide (YM-155) and IL-2 additively decreases tumor weight, lung metastasis, and luciferin-stained tumor images[3].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

Clinical Trial

分子量

398.84

Formula

C20H19ClN4O3

CAS 号

355406-09-6

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Nakahara T, et al. YM155, a novel small-molecule survivin suppressant, induces regression of established human hormone-refractory prostate tumor xenografts. Cancer Res. 2007 Sep 1;67(17):8014-21.

    [2]. Iisa T, et al. Radiosensitizing effect of YM155, a novel small-molecule survivin suppressant, in non-small cell lung cancer cell lines. Clin Cancer Res. 2008 Oct 15;14(20):6496-504.

    [3]. Guo K, et al. A combination of YM-155, a small molecule survivin inhibitor, and IL-2 potently suppresses renal cell carcinoma in murine model. Oncotarget. 2015 Aug 28;6(25):21137-47.

Cell Assay
[1]

The antiproliferative activity of Sepantronium bromide is measured. After treatment with Sepantronium bromide for 48 h, the cell count is determined by sulforhodamine B assay. The GI50 value is calculated by logistic analysis, which is the drug concentration resulting in a 50% reduction in the net protein increase (as measured by sulforhodamine B staining) in control cells during the drug incubation. The assay is done in triplicate, and the mean GI50 value is obtained from the results of four independent assays.

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Administration
[1]

Five-week-old male nude mice (BALB/c nu/nu) are used for the assay. PC-3 cells (2×106-3×106) are injected into the flanks of the mice and allowed to reach a tumor volume of > 100 mm3 in tumor volume (length×width2×0.5). Sepantronium bromide is s.c. administered as a 3-day continuous infusion per week for 2 weeks using an implanted micro-osmotic pump or i.v. administered five times a week for 2 weeks. The percentage of tumor growth inhibition 14 days after initial Sepantronium bromide administration is calculated for each group using the following formula: MTV=100×{1-[(MTV of the treated group on day 14)-(MTV of the treated group on day 0)]/[(MTV of the control group on day 14)-(MTV of the control group on day 0)]}, where MTV is mean tumor volume. For both the frozen tumors and plasma samples, survivin expression levels are analyzed by Western blotting and Sepantronium bromide concentration by high-performance liquid chromatography/triple quadrupole mass spectrometry (LC/MS/MS) using validated methods.

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

参考文献
  • [1]. Nakahara T, et al. YM155, a novel small-molecule survivin suppressant, induces regression of established human hormone-refractory prostate tumor xenografts. Cancer Res. 2007 Sep 1;67(17):8014-21.

    [2]. Iisa T, et al. Radiosensitizing effect of YM155, a novel small-molecule survivin suppressant, in non-small cell lung cancer cell lines. Clin Cancer Res. 2008 Oct 15;14(20):6496-504.

    [3]. Guo K, et al. A combination of YM-155, a small molecule survivin inhibitor, and IL-2 potently suppresses renal cell carcinoma in murine model. Oncotarget. 2015 Aug 28;6(25):21137-47.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Sepantronium bromide(Synonyms: YM-155)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Sepantronium bromide (Synonyms: YM-155) 纯度: ≥98.0%

Sepantronium bromide (YM-155) 是一种 survivin 抑制剂,其 IC50 为 0.54 nM。

Sepantronium bromide(Synonyms: YM-155)

Sepantronium bromide Chemical Structure

CAS No. : 781661-94-7

规格 价格 是否有货 数量
Free Sample (0.1-0.5 mg)   Apply now  
10 mM * 1 mL in DMSO ¥550 In-stock
5 mg ¥500 In-stock
10 mg ¥850 In-stock
50 mg ¥3000 In-stock
100 mg ¥4600 In-stock
200 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

Sepantronium bromide 相关产品

相关化合物库:

  • Drug Repurposing Compound Library Plus
  • Clinical Compound Library Plus
  • Bioactive Compound Library Plus
  • Apoptosis Compound Library
  • Anti-Cancer Compound Library
  • Clinical Compound Library
  • Autophagy Compound Library
  • Drug Repurposing Compound Library
  • Anti-COVID-19 Compound Library
  • Anti-Lung Cancer Compound Library
  • Targeted Diversity Library

生物活性

Sepantronium bromide (YM-155) is a survivin inhibitor with an IC50 of 0.54 nM[1].

IC50 & Target

IC50: 0.54 nM (Survivin)[1]

体外研究
(In Vitro)

Sepantronium bromide (YM155; 30 μM) is not sensitive to survivn gene promoter-driven luciferase reporter activity. Sepantronium bromide shows significant supression on endogenous survivin expression in PC-3 and PPC-1 human HRPC cells with deficient p53 via transcriptional inhibition of the survivin gene promoter. Sepantronium bromide (100 nM) does not affect protein expression of c-IAP2, XIAP, Bcl-2, Bcl-xL, Bad, α-actin, and β-tubulin. Sepantronium bromide potently inhibits human cancer cell lines (mutated or truncated p53) such as PC-3, PPC-1, DU145, TSU-Pr1, 22Rv1, SK-MEL-5 and A375 with IC50s ranging from 2.3 to 11 nM, respectively[1].
Sepantronium bromide (YM155) resultin in an increase in sensitivity of NSCLC cells to γ-radiation. Sepantronium bromide combined with γ-radiation increases both the number of apoptotic cells and the activity of caspase-3. In addition, Sepantronium bromide delays the repair of radiation-induced double-strand breaks in nuclear DNA[2].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

Sepantronium bromide (YM155; 3 and 10 mg/kg) inhibits the tumor growth in PC-3 xenografts, without obvious body weight loss and blood cell count decrease. Sepantronium bromide is highly distributed to tumor tissue in vivo. Sepantronium bromide shows 80% TGI at a dose of 5 mg/kg in PC-3 orthotopic xenografts[1].
Sepantronium bromide (YM155) in combination with γ-radiation shows potent antitumor activity against H460 or Calu6 xenografts in nude mice[2].
In this orthotopic renal and metastatic lung tumors models, Sepantronium bromide (YM-155) and IL-2 additively decreases tumor weight, lung metastasis, and luciferin-stained tumor images[3].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

Clinical Trial

分子量

443.29

Formula

C20H19BrN4O3

CAS 号

781661-94-7

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
In Vitro: 

H2O : 100 mg/mL (225.59 mM; Need ultrasonic)

DMSO : 50 mg/mL (112.79 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.2559 mL 11.2793 mL 22.5586 mL
5 mM 0.4512 mL 2.2559 mL 4.5117 mL
10 mM 0.2256 mL 1.1279 mL 2.2559 mL

*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: PBS

    Solubility: 50 mg/mL (112.79 mM); Clear solution; Need ultrasonic

  • 2.

    请依序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 2 mg/mL (4.51 mM); Clear solution

    此方案可获得 ≥ 2 mg/mL (4.51 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 20.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH₂O 中,得到澄清透明的生理盐水溶液

  • 3.

    请依序添加每种溶剂: 10% DMSO    90% corn oil

    Solubility: 2 mg/mL (4.51 mM); Clear solution; Need ultrasonic

    此方案可获得 2 mg/mL (4.51 mM) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 20.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在 上海金畔生物科技有限公司 网站选购。
参考文献
  • [1]. Nakahara T, et al. YM155, a novel small-molecule survivin suppressant, induces regression of established human hormone-refractory prostate tumor xenografts. Cancer Res. 2007 Sep 1;67(17):8014-21.

    [2]. Iisa T, et al. Radiosensitizing effect of YM155, a novel small-molecule survivin suppressant, in non-small cell lung cancer cell lines. Clin Cancer Res. 2008 Oct 15;14(20):6496-504.

    [3]. Guo K, et al. A combination of YM-155, a small molecule survivin inhibitor, and IL-2 potently suppresses renal cell carcinoma in murine model. Oncotarget. 2015 Aug 28;6(25):21137-47.

Cell Assay
[1]

The antiproliferative activity of Sepantronium bromide is measured. After treatment with Sepantronium bromide for 48 h, the cell count is determined by sulforhodamine B assay. The GI50 value is calculated by logistic analysis, which is the drug concentration resulting in a 50% reduction in the net protein increase (as measured by sulforhodamine B staining) in control cells during the drug incubation. The assay is done in triplicate, and the mean GI50 value is obtained from the results of four independent assays.

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Administration
[1]

Five-week-old male nude mice (BALB/c nu/nu) are used for the assay. PC-3 cells (2×106-3×106) are injected into the flanks of the mice and allowed to reach a tumor volume of > 100 mm3 in tumor volume (length×width2×0.5). Sepantronium bromide is s.c. administered as a 3-day continuous infusion per week for 2 weeks using an implanted micro-osmotic pump or i.v. administered five times a week for 2 weeks. The percentage of tumor growth inhibition 14 days after initial Sepantronium bromide administration is calculated for each group using the following formula: MTV=100×{1-[(MTV of the treated group on day 14)-(MTV of the treated group on day 0)]/[(MTV of the control group on day 14)-(MTV of the control group on day 0)]}, where MTV is mean tumor volume. For both the frozen tumors and plasma samples, survivin expression levels are analyzed by Western blotting and Sepantronium bromide concentration by high-performance liquid chromatography/triple quadrupole mass spectrometry (LC/MS/MS) using validated methods.

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

参考文献
  • [1]. Nakahara T, et al. YM155, a novel small-molecule survivin suppressant, induces regression of established human hormone-refractory prostate tumor xenografts. Cancer Res. 2007 Sep 1;67(17):8014-21.

    [2]. Iisa T, et al. Radiosensitizing effect of YM155, a novel small-molecule survivin suppressant, in non-small cell lung cancer cell lines. Clin Cancer Res. 2008 Oct 15;14(20):6496-504.

    [3]. Guo K, et al. A combination of YM-155, a small molecule survivin inhibitor, and IL-2 potently suppresses renal cell carcinoma in murine model. Oncotarget. 2015 Aug 28;6(25):21137-47.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

YM-201636

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

YM-201636  纯度: 98.01%

YM-201636 是高效选择性的 PIKfyve 抑制剂,IC50 值为 33 nM。YM-201636 也抑制 p110α,IC50 为 3.3 μM。YM-201636 可抑制逆转录病毒复制。

YM-201636

YM-201636 Chemical Structure

CAS No. : 371942-69-7

规格 价格 是否有货 数量
Free Sample (0.1-0.5 mg)   Apply now  
10 mM * 1 mL in DMSO ¥1157 In-stock
2 mg ¥550 In-stock
5 mg ¥1125 In-stock
10 mg ¥2148 In-stock
50 mg ¥6650 In-stock
100 mg ¥10230 In-stock
200 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

YM-201636 相关产品

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  • Anti-Colorectal Cancer Compound Library

生物活性

YM-201636 is a potent and selective PIKfyve inhibitor with an IC50 of 33 nM. YM-201636 also inhibits p110α with an IC50 of 3.3 μM. YM-201636 inhibits retroviral replication.

IC50 & Target

p110α

3.3 μM (IC50)

PIKfyve

33 nM (IC50)

Autophagy

 

体外研究
(In Vitro)

Acute treatment of cells with YM-201636 shows that the PIKfyve pathway is involved in the sorting of endosomal transport, with inhibition leading to the accumulation of a late endosomal compartment and blockade of retroviral exit. The yeast orthologue of PIKfyve, Fab1, is found to be insensitive to YM-201636 (IC50>5 μM). YM-201636 does not inhibit a type IIγ PtdInsP kinase even at 10 μM and inhibits a mouse type Iα PtdInsP kinase with an IC50>2 μM[1]. YM-201636 almost completely inhibits basal and insulin-activated 2-deoxyglucose uptake at doses as low as 160 nM, with IC50=54 nM for the net insulin response. YM-201636 also completely inhibits insulin-dependent activation of class IA PI 3-kinase[2]. At low doses (10-25 nM), YM-201636 inhibits preferentially PtdIns5P rather than PtdIns(3,5)P2 production, whereas at higher doses, the two products are similarly inhibited. YM-201636 at 160 nM inhibits PtdIns5P synthesis twice more effectively compared with PtdIns(3,5)P2 synthesis[3]. MDCK cells treated with YM-201636 accumulate the tight junction protein claudin-1 intracellularly. YM-201636 treatment blocks the continuous recycling of claudin-1/claudin-2 and delays epithelial barrier formation[4].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

467.48

Formula

C25H21N7O3

CAS 号

371942-69-7

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
溶解性数据
In Vitro: 

DMSO : ≥ 47 mg/mL (100.54 mM)

* “≥” means soluble, but saturation unknown.

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.1391 mL 10.6956 mL 21.3913 mL
5 mM 0.4278 mL 2.1391 mL 4.2783 mL
10 mM 0.2139 mL 1.0696 mL 2.1391 mL

*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 2.5 mg/mL (5.35 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (5.35 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH₂O 中,得到澄清透明的生理盐水溶液

  • 2.

    请依序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: 2.5 mg/mL (5.35 mM); Suspended solution; Need ultrasonic

    此方案可获得 2.5 mg/mL (5.35 mM) 的均匀悬浊液,悬浊液可用于口服和腹腔注射。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液中,混合均匀。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
  • 3.

    请依序添加每种溶剂: 10% DMSO    90% corn oil

    Solubility: ≥ 2.5 mg/mL (5.35 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (5.35 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在 上海金畔生物科技有限公司 网站选购。
参考文献
  • [1]. Jefferies HB, et al. A selective PIKfyve inhibitor blocks PtdIns(3,5)P(2) production and disrupts endomembrane transport and retroviral budding. EMBO Rep, 2008, 9(2), 164-170.

    [2]. Ikonomov OC, et al. YM-201636, an inhibitor of retroviral budding and PIKfyve-catalyzed PtdIns(3,5)P2 synthesis, halts glucose entry by insulin in adipocytes. Biochem Biophys Res Commun. 2009 May 8;382(3):566-70.

    [3]. Sbrissa D, et al. Functional dissociation between PIKfyve-synthesized PtdIns5P and PtdIns(3,5)P2 by means of the PIKfyve inhibitor YM-201636. Am J Physiol Cell Physiol. 2012 Aug 15;303(4):C436-46.

    [4]. Dukes JD, et al. The PIKfyve inhibitor YM-201636 blocks the continuous recycling of the tight junction proteins claudin-1 and claudin-2 in MDCK cells. PLoS One. 2012;7(3):e28659.

    [5]. Ikonomov OC, et al. YM201636, an inhibitor of retroviral budding and PIKfyve-catalyzed PtdIns(3,5)P2 synthesis, halts glucose entry by insulin in adipocytes. Biochem Biophys Res Commun. 2009 May 8;382(3):566-70.

Kinase Assay
[2]

Following 3T3L1 adipocyte serum-starvation and insulin stimulation, cell lysates containing protease inhibitors are clarified and then subjected to immunoprecipitation with anti-PIKfyve antibodies. Washed beads are mixed with 100 μM PtdIns and preincubated for 15 min with YM-201636 (100 nM) or vehicle in the assay buffer (50 mM Tris-HCl, pH 7.5, 1 mM EGTA and 10 mM MgCl2). The kinase assay (50 μL final volume) is carried out for 15 min at 37 °C with 15 μM ATP and [γ-32P]ATP (30 μCi). Lipids are extracted, spotted on TLC glass plates (250 μm), resolved by a chloroform/methanol/water/ammonia solvent system and detected by autoradiography[2].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Assay
[4]

YM-201636 is dissolved in DMSO and diluted with DMEM and added to cells at a final concentration of 800 nM. Cells are treated with YM-201636 or a DMSO control for 2 h. For TER measurements cells are plated at confluency on Transwell permeable polyester filters (0.4 µm pore size) with surface area of 0.33 cm2. Media is changed ever 2-3 days and cells are grown for 7 days prior to TER measurements[4].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

参考文献
  • [1]. Jefferies HB, et al. A selective PIKfyve inhibitor blocks PtdIns(3,5)P(2) production and disrupts endomembrane transport and retroviral budding. EMBO Rep, 2008, 9(2), 164-170.

    [2]. Ikonomov OC, et al. YM-201636, an inhibitor of retroviral budding and PIKfyve-catalyzed PtdIns(3,5)P2 synthesis, halts glucose entry by insulin in adipocytes. Biochem Biophys Res Commun. 2009 May 8;382(3):566-70.

    [3]. Sbrissa D, et al. Functional dissociation between PIKfyve-synthesized PtdIns5P and PtdIns(3,5)P2 by means of the PIKfyve inhibitor YM-201636. Am J Physiol Cell Physiol. 2012 Aug 15;303(4):C436-46.

    [4]. Dukes JD, et al. The PIKfyve inhibitor YM-201636 blocks the continuous recycling of the tight junction proteins claudin-1 and claudin-2 in MDCK cells. PLoS One. 2012;7(3):e28659.

    [5]. Ikonomov OC, et al. YM201636, an inhibitor of retroviral budding and PIKfyve-catalyzed PtdIns(3,5)P2 synthesis, halts glucose entry by insulin in adipocytes. Biochem Biophys Res Commun. 2009 May 8;382(3):566-70.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

YM琼脂

上海金畔生物科技有限公司可以定制生产国产培养基,可以访问官网了解更多产品信息。
YM琼脂

英文名称: YM Agar
产品货号: JP0297
产品规格: 250g
155元
保质期: 三年
产品用途: 用于霉菌,酵母菌及耐酸菌的分离培养
备  注:

产品介绍:

用途:用于霉菌、酵母菌的分离培养。

原理:酪蛋白胨,麦芽浸粉,酵母浸粉提供碳源、氮源,维生素和其他生长因子;葡萄糖为可发酵糖类;琼脂是凝固剂。

用法

称取本品 41.0g,加热溶解于 1000ml 蒸馏水中,115℃高压灭菌  20 分钟,备用。

细菌在YM琼脂上的生长特征

A为白色念珠菌;B为酵母菌;C为黑曲霉菌

YM琼脂微生物灵敏度试验:

按标签用法制备培养基,接种以下质控菌株,放置20-25℃需氧培养48-72小时。
注:回收率计算时,用SDA琼脂做对照培养基。

YM琼脂培养基原理及实验现象 https://www.hopebiol.com/asphtml/refere10841.htm


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YM11琼脂

上海金畔生物科技有限公司可以定制生产国产培养基,可以访问官网了解更多产品信息。
YM11琼脂

英文名称: YM11 Agar
产品货号: JP0298
产品规格: 250g
185元
保质期: 三年
产品用途: 滤膜法用于霉菌,酵母菌的分离培养(NEOGEN)
备  注:

产品介绍:

用途:滤膜法用于霉菌,酵母菌的分离培养(NEOGEN)。

成分(g/L)

大豆蛋白胨 
胰酪蛋白胨 
葡萄糖 
氯化钠 
磷酸氢二钾 
台盼兰 
氯霉素 
琼脂 
PH7.0±0.2  
20.0g 
20.0g 
5.0g 
5.0g 
2.4g 
0.03g 
0.1g 
15.0g 
25℃
用法:称取本品47.5克,加热溶解于1000ml蒸馏水中,121℃高压灭菌15分钟,备用
质量控制和典型特征:在28℃培养48-72小时,酵母菌显蓝色菌落,霉菌显蓝灰色菌落。

OGY琼脂微生物灵敏度试验:

按标签用法制备培养基,接种以下质控菌株,放置22±3℃需氧培养48-72小时。
注:回收率计算时,用SDA琼脂做对照培养基。


YM11琼脂相关产品:

产品货号 产品名称 产品规格 产品说明及用途
JP9202 BSM培养基基础
BSM Medium Base
250g 用于酵母菌的表达
JP8869 麦芽汁牛肉膏蛋白胨琼脂平板培养基
Wort Beef Extract Peptone Agar Medium
250g 用于酵母菌的培养
JP9141 牛肉膏蛋白胨培养基(BPM)
Beef extract Peptone Medium
250g
JP0231 察氏琼脂
Czapek Dox Agar
250g 用于青霉,曲霉鉴定及保存菌种用(GB标准)
JP0232 产毒培养基
Toxin-Producing Medium
250g 用于青霉,曲霉的产毒培养
JP0234 高盐察氏琼脂
Salt Czapek Dox Agar
250g 用于霉菌和酵母菌的计数(GB标准)
JP0236 玉米粉琼脂
Corn Meal Medium
250g 用于真菌培养
JP0237-2 孟加拉红琼脂
Rose Bengal Medium
250g 用于食品中霉菌及酵母菌总数测定
JP4176 麦芽浸膏汤
Malt Extract Broth
200g 用于酸性罐头食品商业无菌检测
JP0287 酵母粉葡萄糖氯霉素琼脂(YDC)
Yeast Extract Dextrose Chloramphenicol Agar
250g 用于食品中霉菌及酵母菌总数测定(ISO标准)
JP0288 Candida Elective琼脂
Candida Elective Agar
250g 用于食品中念珠菌及酵母菌总数测定
JP0289 DTM培养基
DTM Medium
250g 用于食品中真菌的培养
JP0290 DRBC琼脂
DRBC Agar
250g 用于食品中霉菌及酵母菌分离培养
JP0291 WORT琼脂
Wort Agar
250g 用于真菌,特别是酵母菌的计数和增菌培养
JP0292 WORT肉汤
Wort Broth
250g 用于真菌,特别是酵母菌的培养
JP0293 YGC琼脂
YGC Agar
250g 用于奶和奶制品中霉菌及酵母菌分离培养(ISO方法)
JP0294 改良绿色酵母菌和真菌肉汤(M-Green Yeast and Fungi Broth)
M-Green Yeast and Fungi Broth
250g 用于饮料中真菌及酵母菌检测
JP0295 Littman琼脂
Littman Agar
250g 用于真菌的分离培养
JP0296 DG-18琼脂
DG-18 Agar
250g 用于食品中霉菌和酵母菌分离培养
JP0297 YM琼脂
YM Agar
250g 用于霉菌,酵母菌及耐酸菌的分离培养
JP0299 OGY琼脂
OGY Agar
250g 用于霉菌和酵母菌分离培养和计数
JP0300 WL营养琼脂
WL Nutrient Agar
250g 用于啤酒和发酵产品中酵母菌和细菌的计数
JP0301 改良沙氏琼脂培养基
Sabouraud’s Agar,Modified
250g 用于真菌培养
JP0302 沙氏BHI琼脂
Sabouraud BHI Agar
250g 用于真菌检测
JP8657 高渗真菌学琼脂
Osmophilic Mycophile Agar
250g 用于高渗食品中酵母菌和霉菌检测
JP0233-5 马铃薯葡萄糖琼脂(含氯霉素)
Potato Dextrose Agar(Chloramphenicol)
250 用于霉菌和酵母菌的计数和分离培养
JP8690 BIGGY琼脂
BIGGY Agar
250g 用于念珠菌的分离培养和计数
JP0236-1 1%吐温80-玉米琼脂培养基
1%Tween80-Corn Meat Agar Mediun
250g 用于白色念珠菌产芽管试验
JP0235-6 SDAY培养基
SDAY
250g 用于真菌的分离培养
JP4176-1 麦芽浸膏琼脂
Malt Extract Agar
200g 用于霉菌和酵母菌的分离培养和计数
JP8615 皮肤癣菌鉴别琼脂(DTM)
DTM Agar
250g 用于皮肤癣菌鉴别培养
JP8531 酵母浸出物葡萄糖土霉素琼脂培养基
Yeast Extract Glucose Oxytetracycline Agar
250g 用于乳和乳制品中酵母菌和霉菌的计数
JP8712 马铃薯-蔗糖培养基
Potato sucrose Medium
250g 用于霉菌培养
JP8717 酵母蛋白胨培养基
Yeast Extract Peptone
250g 用于真菌的培养
JP4176-2 麦芽汁琼脂
Malt Extract Agar
250g 用于霉菌和酵母菌计数
JP0297-1 YM培养基
YM Medium
250g 用于霉菌和酵母菌的增菌培养
JP8729 WLN培养基
WLN Medium
250g 用于酿造和工业发酵过程中细菌、酵母菌和霉菌培养
JP0296-1 氯硝胺18%甘油(DG18)琼脂
DG18 Agar
250g 用于蜂蜜中嗜渗酵母计数
JP8751 30%葡萄糖溶液(PH6.5±0.5)
30% Dextrose Broth
250g 用于嗜渗酵母检验时的样品稀释(GB标准)
JP8753 0.1%吕氏碱性美蓝染色液 5ml*6支/盒 用于酵母菌镜检染色
JP8755 YPDA培养基
YPDA Medium
250g 用于酵母菌增菌培养
JP8615a DTM添加剂1 1ml*5 每支添加于200mlDTM培养基中
JP8615b DTM添加剂2 1ml*5 每支添加于200mlDTM培养基中
JP8757 氯霉素麦芽提取物琼脂培养基 250g 用于真菌的分离培养
JP0231-1 察氏液体培养基 250g 用于测定真菌孢子发芽率
JP0233-8 马铃薯液体培养基(含氯霉素)
Potato liquid medium
250g 用于霉菌和酵母菌增菌培养
JP8764 改良察氏液体培养基
Modified Czapek Dox Broth Medium
250g 用于霉菌的增菌培养
JP8765 面包酵母标准培养基 250g 用于面包酵母计数培养
JP8766 野生酵母培养基 250g 用于野生酵母计数培养
JP8775 土霉素麦芽提取物琼脂培养基 250g 用于真菌的分离培养
JP4702-1 霉菌培养基(含琼脂和氯霉素)
Fungal Medium
250g 用于霉菌的分离培养
JP0235-11 沙氏葡萄糖琼脂培养基(含氯霉素)(USP)(Sabouraud-glucose Agar with Chloramphenicol)
Sabouraud-glucose Agar with Chloramphenicol
250g 用于霉菌和酵母菌的分离培养
JP8814 赖氨酸培养基(LYS)
Lysine Medium
250g 用于野生酿酒酵母的分离
JP0233 马铃薯葡萄糖琼脂(PDA)
Potato Dextrose Agar
250g 用于霉菌,酵母菌计数(GB/SN标准)
JP0233-3 马铃薯琼脂培养基
Potato Agar Medium
250g 用于霉菌的鉴定培养
JP0233-4 马铃薯葡萄糖水
Potato Dextrose Water
250g 用于椰毒假单胞酵米面亚种和真菌的增菌培养
JP0233-6 综合马铃薯培养基
Intergrated Potato Medium
250g 用于真菌的分离培养
JP4176-3 麦芽汁培养基
Malt Extract Medium
250g 用于霉菌和酵母菌增菌培养
JP5193-1 YPD液体培养基
YPD Broth
250g 用于酵母菌的增菌培养
JP0235-1 沙氏葡萄糖琼脂(USP)(Sabouraud Dextrose Agar Medium)
Sabouraud Dextrose Agar Medium
250g 用于霉菌和酵母菌的分离培养
JP8315-2 酪蛋白葡萄糖琼脂
Sabouraud Dextrose Agar
250g 用于霉菌、酵母菌等的分离培养
JP8407-2 沙氏葡萄糖琼脂(含氯霉素)(EP标准)
Sabouraud-glucose Agar with Chloramphenicol
250g 用于霉菌和酵母菌的分离培养
JP8567-1 酪蛋白葡萄糖肉汤
Sabouraud-dextrose Broth
250g 用于霉菌、酵母菌等的增菌培养
JP8617 大豆胨酵母浸粉琼脂(PYE)
Phytone Yeast Extract Agar
250g 用于真菌的选择性分离培养
JP8730 WLD培养基
WLD Medium
250g 用于酿造和工业发酵过程中细菌分离培养
JP8733 不完全琼脂培养基
Incomplete Agar Medium
250g 用于纺织品微真菌影响评价试验
JP8746 ISP培养基2
ISP Medium 2
250g 用于链霉菌培养和鉴别
JP0296-1a 氯霉素溶液(20mg) 1ml*5 每支添加于200ml氯硝胺18%甘油(DG18)琼脂中
JP8829-1 LG培养基
(Linden Grain Medium)
250g 用于霉菌、酵母菌、耐热霉菌及细菌总数的检测,可用于PET瓶及无菌罐装生产线的无菌验证。
JP0237-3 虎红(孟加拉红)培养基
Rose Bengal Medium
250g 用于霉菌和酵母菌总数的确定(2015版化妆品规范)
JP8892 麦芽浸粉琼脂培养基
Malt Extract Agar Medium
250g 用于霉菌和酵母菌的分离、培养和计数
JP0233-1 马铃薯葡萄糖琼脂(高校专用)
Potato Dextrose Agar
250g 用于霉菌和酵母菌的计数,本品为高澄清度,39g/L
JP0235-13 沙氏琼脂(含氯霉素)
Sabouraud Agar Chloramphenicol Medium(SABC)
250g 用于酵母菌和霉菌计数
JP8671 马丁培养基
Martin Medium
250g 用于测定磷细菌肥料中霉菌数
JP8826 ISP培养基6
ISP Medium 6
250g 用于链霉菌的培养

YM培养基

上海金畔生物科技有限公司可以定制生产国产培养基,可以访问官网了解更多产品信息。
YM培养基

英文名称: YM Medium
产品货号: JP0297-1
产品规格: 250g
150元
保质期: 三年
产品用途: 用于霉菌和酵母菌的增菌培养
备  注:

产品介绍:

用途:用于霉菌和酵母菌的增菌培养。

用法

称取本品 21.0g,加热溶解于 1000ml 蒸馏水中,121℃高压灭菌  15 分钟,备用。

YM培养基微生物灵敏度试验:

按标签用法制备培养基,接种以下质控菌株,放置20-25℃需氧培养48-72小时。


YM培养基相关产品:

产品货号 产品名称 产品规格 产品说明及用途
JP9202 BSM培养基基础
BSM Medium Base
250g 用于酵母菌的表达
JP8869 麦芽汁牛肉膏蛋白胨琼脂平板培养基
Wort Beef Extract Peptone Agar Medium
250g 用于酵母菌的培养
JP9141 牛肉膏蛋白胨培养基(BPM)
Beef extract Peptone Medium
250g
JP0231 察氏琼脂
Czapek Dox Agar
250g 用于青霉,曲霉鉴定及保存菌种用(GB标准)
JP0232 产毒培养基
Toxin-Producing Medium
250g 用于青霉,曲霉的产毒培养
JP0234 高盐察氏琼脂
Salt Czapek Dox Agar
250g 用于霉菌和酵母菌的计数(GB标准)
JP0236 玉米粉琼脂
Corn Meal Medium
250g 用于真菌培养
JP0237-2 孟加拉红琼脂
Rose Bengal Medium
250g 用于食品中霉菌及酵母菌总数测定
JP4176 麦芽浸膏汤
Malt Extract Broth
200g 用于酸性罐头食品商业无菌检测
JP0287 酵母粉葡萄糖氯霉素琼脂(YDC)
Yeast Extract Dextrose Chloramphenicol Agar
250g 用于食品中霉菌及酵母菌总数测定(ISO标准)
JP0288 Candida Elective琼脂
Candida Elective Agar
250g 用于食品中念珠菌及酵母菌总数测定
JP0289 DTM培养基
DTM Medium
250g 用于食品中真菌的培养
JP0290 DRBC琼脂
DRBC Agar
250g 用于食品中霉菌及酵母菌分离培养
JP0291 WORT琼脂
Wort Agar
250g 用于真菌,特别是酵母菌的计数和增菌培养
JP0292 WORT肉汤
Wort Broth
250g 用于真菌,特别是酵母菌的培养
JP0293 YGC琼脂
YGC Agar
250g 用于奶和奶制品中霉菌及酵母菌分离培养(ISO方法)
JP0294 改良绿色酵母菌和真菌肉汤(M-Green Yeast and Fungi Broth)
M-Green Yeast and Fungi Broth
250g 用于饮料中真菌及酵母菌检测
JP0295 Littman琼脂
Littman Agar
250g 用于真菌的分离培养
JP0296 DG-18琼脂
DG-18 Agar
250g 用于食品中霉菌和酵母菌分离培养
JP0297 YM琼脂
YM Agar
250g 用于霉菌,酵母菌及耐酸菌的分离培养
JP0298 YM11琼脂
YM11 Agar
250g 滤膜法用于霉菌,酵母菌的分离培养(NEOGEN)
JP0299 OGY琼脂
OGY Agar
250g 用于霉菌和酵母菌分离培养和计数
JP0300 WL营养琼脂
WL Nutrient Agar
250g 用于啤酒和发酵产品中酵母菌和细菌的计数
JP0301 改良沙氏琼脂培养基
Sabouraud’s Agar,Modified
250g 用于真菌培养
JP0302 沙氏BHI琼脂
Sabouraud BHI Agar
250g 用于真菌检测
JP8657 高渗真菌学琼脂
Osmophilic Mycophile Agar
250g 用于高渗食品中酵母菌和霉菌检测
JP0233-5 马铃薯葡萄糖琼脂(含氯霉素)
Potato Dextrose Agar(Chloramphenicol)
250 用于霉菌和酵母菌的计数和分离培养
JP8690 BIGGY琼脂
BIGGY Agar
250g 用于念珠菌的分离培养和计数
JP0236-1 1%吐温80-玉米琼脂培养基
1%Tween80-Corn Meat Agar Mediun
250g 用于白色念珠菌产芽管试验
JP0235-6 SDAY培养基
SDAY
250g 用于真菌的分离培养
JP4176-1 麦芽浸膏琼脂
Malt Extract Agar
200g 用于霉菌和酵母菌的分离培养和计数
JP8615 皮肤癣菌鉴别琼脂(DTM)
DTM Agar
250g 用于皮肤癣菌鉴别培养
JP8531 酵母浸出物葡萄糖土霉素琼脂培养基
Yeast Extract Glucose Oxytetracycline Agar
250g 用于乳和乳制品中酵母菌和霉菌的计数
JP8712 马铃薯-蔗糖培养基
Potato sucrose Medium
250g 用于霉菌培养
JP8717 酵母蛋白胨培养基
Yeast Extract Peptone
250g 用于真菌的培养
JP4176-2 麦芽汁琼脂
Malt Extract Agar
250g 用于霉菌和酵母菌计数
JP8729 WLN培养基
WLN Medium
250g 用于酿造和工业发酵过程中细菌、酵母菌和霉菌培养
JP0296-1 氯硝胺18%甘油(DG18)琼脂
DG18 Agar
250g 用于蜂蜜中嗜渗酵母计数
JP8751 30%葡萄糖溶液(PH6.5±0.5)
30% Dextrose Broth
250g 用于嗜渗酵母检验时的样品稀释(GB标准)
JP8753 0.1%吕氏碱性美蓝染色液 5ml*6支/盒 用于酵母菌镜检染色
JP8755 YPDA培养基
YPDA Medium
250g 用于酵母菌增菌培养
JP8615a DTM添加剂1 1ml*5 每支添加于200mlDTM培养基中
JP8615b DTM添加剂2 1ml*5 每支添加于200mlDTM培养基中
JP8757 氯霉素麦芽提取物琼脂培养基 250g 用于真菌的分离培养
JP0231-1 察氏液体培养基 250g 用于测定真菌孢子发芽率
JP0233-8 马铃薯液体培养基(含氯霉素)
Potato liquid medium
250g 用于霉菌和酵母菌增菌培养
JP8764 改良察氏液体培养基
Modified Czapek Dox Broth Medium
250g 用于霉菌的增菌培养
JP8765 面包酵母标准培养基 250g 用于面包酵母计数培养
JP8766 野生酵母培养基 250g 用于野生酵母计数培养
JP8775 土霉素麦芽提取物琼脂培养基 250g 用于真菌的分离培养
JP4702-1 霉菌培养基(含琼脂和氯霉素)
Fungal Medium
250g 用于霉菌的分离培养
JP0235-11 沙氏葡萄糖琼脂培养基(含氯霉素)(USP)(Sabouraud-glucose Agar with Chloramphenicol)
Sabouraud-glucose Agar with Chloramphenicol
250g 用于霉菌和酵母菌的分离培养
JP8814 赖氨酸培养基(LYS)
Lysine Medium
250g 用于野生酿酒酵母的分离
JP0233 马铃薯葡萄糖琼脂(PDA)
Potato Dextrose Agar
250g 用于霉菌,酵母菌计数(GB/SN标准)
JP0233-3 马铃薯琼脂培养基
Potato Agar Medium
250g 用于霉菌的鉴定培养
JP0233-4 马铃薯葡萄糖水
Potato Dextrose Water
250g 用于椰毒假单胞酵米面亚种和真菌的增菌培养
JP0233-6 综合马铃薯培养基
Intergrated Potato Medium
250g 用于真菌的分离培养
JP4176-3 麦芽汁培养基
Malt Extract Medium
250g 用于霉菌和酵母菌增菌培养
JP5193-1 YPD液体培养基
YPD Broth
250g 用于酵母菌的增菌培养
JP0235-1 沙氏葡萄糖琼脂(USP)(Sabouraud Dextrose Agar Medium)
Sabouraud Dextrose Agar Medium
250g 用于霉菌和酵母菌的分离培养
JP8315-2 酪蛋白葡萄糖琼脂
Sabouraud Dextrose Agar
250g 用于霉菌、酵母菌等的分离培养
JP8407-2 沙氏葡萄糖琼脂(含氯霉素)(EP标准)
Sabouraud-glucose Agar with Chloramphenicol
250g 用于霉菌和酵母菌的分离培养
JP8567-1 酪蛋白葡萄糖肉汤
Sabouraud-dextrose Broth
250g 用于霉菌、酵母菌等的增菌培养
JP8617 大豆胨酵母浸粉琼脂(PYE)
Phytone Yeast Extract Agar
250g 用于真菌的选择性分离培养
JP8730 WLD培养基
WLD Medium
250g 用于酿造和工业发酵过程中细菌分离培养
JP8733 不完全琼脂培养基
Incomplete Agar Medium
250g 用于纺织品微真菌影响评价试验
JP8746 ISP培养基2
ISP Medium 2
250g 用于链霉菌培养和鉴别
JP0296-1a 氯霉素溶液(20mg) 1ml*5 每支添加于200ml氯硝胺18%甘油(DG18)琼脂中
JP8829-1 LG培养基
(Linden Grain Medium)
250g 用于霉菌、酵母菌、耐热霉菌及细菌总数的检测,可用于PET瓶及无菌罐装生产线的无菌验证。
JP0237-3 虎红(孟加拉红)培养基
Rose Bengal Medium
250g 用于霉菌和酵母菌总数的确定(2015版化妆品规范)
JP8892 麦芽浸粉琼脂培养基
Malt Extract Agar Medium
250g 用于霉菌和酵母菌的分离、培养和计数
JP0233-1 马铃薯葡萄糖琼脂(高校专用)
Potato Dextrose Agar
250g 用于霉菌和酵母菌的计数,本品为高澄清度,39g/L
JP0235-13 沙氏琼脂(含氯霉素)
Sabouraud Agar Chloramphenicol Medium(SABC)
250g 用于酵母菌和霉菌计数
JP8671 马丁培养基
Martin Medium
250g 用于测定磷细菌肥料中霉菌数
JP8826 ISP培养基6
ISP Medium 6
250g 用于链霉菌的培养

三申YM100不锈钢立式电热蒸汽灭菌器

三申YM100不锈钢立式电热蒸汽灭菌器

  • 品牌 三申|sanshen
  • 型号 YM100
  • 商品详情

    产品介绍

    1、不锈钢材质制成,经久耐用;
    2、轻启翻盖结构,上盖自动弹起,轻松省力;
    3、控制面板的斜面设计,便于观察操作;
    4、微电脑程序控制灭菌程序中的加热和计时过程;
    5、LED数码管和指示灯,动态显示设备运行状态;
    6、电脑板具有PID功能,通过自整定修正加热参数,可以防止冲温,控温精度达到±0.5℃以内;
    7、低水位自动补水功能,且有声光报警系统,补完水自动恢复加热;
    8、重力排汽法设计,腔内纯蒸汽环境,灭菌效果可靠;
    9、径向自胀式硅橡胶密封圈,密封效果好,使用寿命长;
    10、温度超过设定值2℃,自动停止加热,同时声光报警;
    11、超压到0.17MPa安全阀自动泄放蒸汽,保护设备;
    12、放水阀可以排放桶内浓缩水,防止结垢;
    13、带刹车的万向脚轮移位轻捷,定位方便;
    14、浸入式电加热管,热效率高。

    主要技术参数(Main Technical Data)

    型号 原型号 工作电源 功率(kW) 容积(L) 补水压力(MPa) 工作压力(MPa) 工作温度(℃) 保温时间 器内温差(℃) 外形尺寸(cm) 包装尺寸(木)(cm)
    YM30 YM30Z/YX350Z ~220V/50Hz 3 30 ≥0.2≤0.4 随温度 室温 +5~126自选 1~99.59min/h <1 70*×51×73 77×65×82
    YM50 YM50Z/YX400Z 50 70×51×82 77×65×96
    YM75 YM75Z/YX450Z 75 70×51×93 77×65×106
    YM100 YM100Z/YX450Z 3.8 100 70×51×104 77×65×116


  • 上光六厂金相试样预磨机YM-2A

    上光六厂金相试样预磨机YM-2A

  • 品牌 上光六厂|SOIF
  • 型号 YM-2A
  • 商品详情

    在金相试样制备过程中,试样的预磨,是抛光前必不可少的前道工序,先将试样预磨光后,可大大提高试样制备的功效,YM-2A预磨机,是通过对多方面的调研和采集多方面使用人员的意见及要求设计而成。

    技术参数:    

    磨盘直径 

    双盘 230 mm

    砂纸直径

    230mm

    转  速

    400r/min,500r/min(630r/min,780r/min定制)

    电 动 机

    YSR7146 0.55kW 380V 50Hz

    外形尺寸

    755*650*300mm

    重    量

    44Kg

  • 上光六厂金相试样预磨机YM-1A

    上光六厂金相试样预磨机YM-1A

  • 品牌 上光六厂|SOIF
  • 型号 YM-1A
  • 商品详情

    显微镜特点:
    在金相试样制备过程中,试样的预磨,是抛光前必不可少的前道工序,先将试样预磨光后,可大大提高试样制备的工效,YM-1A预磨机,是通过对多方预磨的需要,该机的磨盘直径大于国内同类产品,磨盘的转速也不同于国内产品,是试样预磨的优选设备。

    技术参数:

    磨盘直径 

    230mm

    砂纸直径

    230mm

    转  速

    700r/min

    电 动 机

    YS7118,0.2KW,380V,50Hz

    外形尺寸

    650*340*300mm

    重    量

    36kg

  • 上光六厂金相试样预磨机YM-1

    上光六厂金相试样预磨机YM-1

  • 品牌 上光六厂|SOIF
  • 型号 YM-1
  • 商品详情

    在金相试样制备过程中,试样的预磨,是抛光前必不可少的前道工序,先将试样预磨光后,可大大提高试样制备的工效,YM-1A预磨机,是通过对多方预磨的需要,该机的磨盘直径大于国内同类产品,磨盘的转速也不同于国内产品,是试样预磨的优选设备。

    技术参数:

    磨盘直径 

    230mm

    砂纸直径

    230mm

    转  速

    900r / min

    电 动 机

    YS7118,0.2KW,380V,50Hz

    外形尺寸

    460×3400×330mm

    重    量

    22 kg

  • 三申YM75 不锈钢立式电热蒸汽灭菌器

    三申YM75 不锈钢立式电热蒸汽灭菌器

  • 品牌 三申|sanshen
  • 型号 YM75(YM75Z/YX-450Z)
  • 商品详情

    产品介绍

    1、不锈钢材质制成,经久耐用;
    2、轻启翻盖结构,上盖自动弹起,轻松省力;
    3、控制面板的斜面设计,便于观察操作;
    4、微电脑程序控制灭菌程序中的加热和计时过程;
    5、LED数码管和指示灯,动态显示设备运行状态;
    6、电脑板具有PID功能,通过自整定修正加热参数,可以防止冲温,控温精度达到±0.5℃以内;
    7、低水位自动补水功能,且有声光报警系统,补完水自动恢复加热;
    8、重力排汽法设计,腔内纯蒸汽环境,灭菌效果可靠;
    9、径向自胀式硅橡胶密封圈,密封效果好,使用寿命长;
    10、温度超过设定值2℃,自动停止加热,同时声光报警;
    11、超压到0.17MPa安全阀自动泄放蒸汽,保护设备;
    12、放水阀可以排放桶内浓缩水,防止结垢;
    13、带刹车的万向脚轮移位轻捷,定位方便;
    14、浸入式电加热管,热效率高。

    主要技术参数(Main Technical Data)

    型号 原型号 工作电源 功率(kW) 容积(L) 补水压力(MPa) 工作压力(MPa) 工作温度(℃) 保温时间 器内温差(℃) 外形尺寸(cm) 包装尺寸(木)(cm)
    YM30 YM30Z/YX350Z ~220V/50Hz 3 30 ≥0.2≤0.4 随温度 室温 +5~126自选 1~99.59min/h <1 70*×51×73 77×65×82
    YM50 YM50Z/YX400Z 50 70×51×82 77×65×96
    YM75 YM75Z/YX450Z 75 70×51×93 77×65×106
    YM100 YM100Z/YX450Z 3.8 100 70×51×104 77×65×116


  • 三申YM50不锈钢立式电热蒸汽灭菌器

    三申YM50不锈钢立式电热蒸汽灭菌器

  • 品牌 三申|sanshen
  • 型号 YM50(YM50Z/YX-400Z)
  • 商品详情

    产品介绍

    1、不锈钢材质制成,经久耐用;
    2、轻启翻盖结构,上盖自动弹起,轻松省力;
    3、控制面板的斜面设计,便于观察操作;
    4、微电脑程序控制灭菌程序中的加热和计时过程;
    5、LED数码管和指示灯,动态显示设备运行状态;
    6、电脑板具有PID功能,通过自整定修正加热参数,可以防止冲温,控温精度达到±0.5℃以内;
    7、低水位自动补水功能,且有声光报警系统,补完水自动恢复加热;
    8、重力排汽法设计,腔内纯蒸汽环境,灭菌效果可靠;
    9、径向自胀式硅橡胶密封圈,密封效果好,使用寿命长;
    10、温度超过设定值2℃,自动停止加热,同时声光报警;
    11、超压到0.17MPa安全阀自动泄放蒸汽,保护设备;
    12、放水阀可以排放桶内浓缩水,防止结垢;
    13、带刹车的万向脚轮移位轻捷,定位方便;
    14、浸入式电加热管,热效率高。

    主要技术参数(Main Technical Data)

    型号 原型号 工作电源 功率(kW) 容积(L) 补水压力(MPa) 工作压力(MPa) 工作温度(℃) 保温时间 器内温差(℃) 外形尺寸(cm) 包装尺寸(木)(cm)
    YM30 YM30Z/YX350Z ~220V/50Hz 3 30 ≥0.2≤0.4 随温度 室温 +5~126自选 1~99.59min/h <1 70*×51×73 77×65×82
    YM50 YM50Z/YX400Z 50 70×51×82 77×65×96
    YM75 YM75Z/YX450Z 75 70×51×93 77×65×106
    YM100 YM100Z/YX450Z 3.8 100 70×51×104 77×65×116


  • 三申YM30不锈钢立式电热蒸汽灭菌器

    三申YM30不锈钢立式电热蒸汽灭菌器

  • 品牌 三申|sanshen
  • 型号 YM30(YM30Z/YX-350Z)
  • 商品详情

    产品介绍

    1、不锈钢材质制成,经久耐用;
    2、轻启翻盖结构,上盖自动弹起,轻松省力;
    3、控制面板的斜面设计,便于观察操作;
    4、微电脑程序控制灭菌程序中的加热和计时过程;
    5、LED数码管和指示灯,动态显示设备运行状态;
    6、电脑板具有PID功能,通过自整定修正加热参数,可以防止冲温,控温精度达到±0.5℃以内;
    7、低水位自动补水功能,且有声光报警系统,补完水自动恢复加热;
    8、重力排汽法设计,腔内纯蒸汽环境,灭菌效果可靠;
    9、径向自胀式硅橡胶密封圈,密封效果好,使用寿命长;
    10、温度超过设定值2℃,自动停止加热,同时声光报警;
    11、超压到0.17MPa安全阀自动泄放蒸汽,保护设备;
    12、放水阀可以排放桶内浓缩水,防止结垢;
    13、带刹车的万向脚轮移位轻捷,定位方便;
    14、浸入式电加热管,热效率高。


    主要技术参数(Main Technical Data)

    型号 原型号 工作电源 功率(kW) 容积(L) 补水压力(MPa) 工作压力(MPa) 工作温度(℃) 保温时间 器内温差(℃) 外形尺寸(cm) 包装尺寸(木)(cm)
    YM30 YM30Z/YX350Z ~220V/50Hz 3 30 ≥0.2≤0.4 随温度 室温 +5~126自选 1~99.59min/h <1 70*×51×73 77×65×82
    YM50 YM50Z/YX400Z 50 70×51×82 77×65×96
    YM75 YM75Z/YX450Z 75 70×51×93 77×65×106
    YM100 YM100Z/YX450Z 3.8 100 70×51×104 77×65×116

  • Minodronic acid(Synonyms: YM-529)

    上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

    Minodronic acid (Synonyms: YM-529) 纯度: ≥98.0%

    Minodronic acid (YM-529) 是第三代二磷酸盐,直接或间接地阻止增殖,诱导细胞凋亡,并抑制各种类型的癌细胞的转移。Minodronic acid (YM-529) 是一种参与疼痛的嘌呤 P2X2/3 受体拮抗剂。

    Minodronic acid(Synonyms: YM-529)

    Minodronic acid Chemical Structure

    CAS No. : 180064-38-4

    规格 价格 是否有货 数量
    10 mM * 1 mL in Water ¥550 In-stock
    10 mg ¥500 In-stock
    50 mg ¥1500 In-stock
    100 mg ¥2500 In-stock
    200 mg   询价  
    500 mg   询价  

    * Please select Quantity before adding items.

    Minodronic acid 相关产品

    相关化合物库:

    • Drug Repurposing Compound Library Plus
    • Clinical Compound Library Plus
    • Bioactive Compound Library Plus
    • Apoptosis Compound Library
    • Membrane Transporter/Ion Channel Compound Library
    • Anti-Cancer Compound Library
    • Clinical Compound Library
    • Drug Repurposing Compound Library
    • Neurotransmitter Receptor Compound Library
    • Rare Diseases Drug Library

    生物活性

    Minodronic acid (YM-529) is a third-generation bisphosphonate that directly and indirectly prevents proliferation, induces apoptosis, and inhibits metastasis of various types of cancer cells. Minodronic acid (YM-529) is an antagonist of purinergic P2X2/3 receptors involved in pain[1][2].

    IC50 & Target

    P2X2/3[2]

    Clinical Trial

    分子量

    322.15

    Formula

    C9H12N2O7P2

    CAS 号

    180064-38-4

    中文名称

    米诺磷酸

    运输条件

    Room temperature in continental US; may vary elsewhere.

    储存方式
    Powder -20°C 3 years
    4°C 2 years
    In solvent -80°C 6 months
    -20°C 1 month
    溶解性数据
    In Vitro: 

    H2O : 5 mg/mL (15.52 mM; Need ultrasonic and warming)

    DMSO : < 1 mg/mL (insoluble or slightly soluble)

    配制储备液
    浓度 溶剂体积 质量 1 mg 5 mg 10 mg
    1 mM 3.1041 mL 15.5207 mL 31.0414 mL
    5 mM 0.6208 mL 3.1041 mL 6.2083 mL
    10 mM 0.3104 mL 1.5521 mL 3.1041 mL

    *

    请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
    储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

    参考文献
    • [1]. Sato K, et al. A third-generation bisphosphonate, minodronic acid (YM529), successfully prevented the growth of bladder cancer in vitro and in vivo. Br J Cancer. 2006 Nov 20;95(10):1354-61.

      [2]. Tanaka M, et al. Minodronic acid induces morphological changes in osteoclasts at bone resorption sites and reaches a level required for antagonism of purinergic P2X2/3 receptors. J Bone Miner Metab. 2018 Jan;36(1):54-63.

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