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商品详细美卓/A83-01/25mg/401002
美卓/A83-01/25mg/401002
美卓/A83-01/25mg/401002
商品编号: 401002
品牌: MedKoo
市场价: ¥4300.00
美元价: 2580.00
产地: 美国(厂家直采)
公司:
产品分类: 多肽合成
公司分类: peptide
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

A83-01
featured

We are open as normal during holiday season. We are only closed in Dec 24, Dec 25 and Jan 1. Orders received during Dec 22 ~ Dec 31 will be shipped out in Jan 4 (same day shipping out is also available upon request).

WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#:401002

CAS#:909910-43-6

Description:A-83-01 is an ALK inhibibitor. It was found that A-83-01 inhibited the transcriptional activity induced by TGF-beta type I receptor ALK-5 and that by activin type IB receptor ALK-4 and nodal type I receptor ALK-7, the kinase domains of which are structurally highly related to those of ALK-5. A-83-01 was found to be more potent in the inhibition of ALK5 than a previously described ALK-5 inhibitor, SB-431542, and also to prevent phosphorylation of Smad2/3 and the growth inhibition induced by TGF-beta. A-83-01 inhibited the epithelial-to-mesenchymal transition induced by TGF-beta, suggesting that A-83-01 and related molecules may be useful for preventing the progression of advanced cancers.

Price and Availability

SizePriceShipping out timeQuantity
1mgUSD 2152 Weeks
5mgUSD 3402 Weeks
10mgUSD 5452 Weeks
25mgUSD 8252 Weeks
Inquire bulk and customized quantity

Pricing updated 2020-12-23.Prices are subject to change without notice.

A83-01, purity > 98%, is in stock. Current shipping out time is about 2 weeks after order is received. CoA, QC data and MSDS documents are available in one week after order is received.

Chemical Structure

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Theoretical Analysis

MedKoo Cat#: 401002Name: A83-01CAS#: 909910-43-6Chemical Formula: C25H19N5SExact Mass: 421.13612Molecular Weight: 421.52Elemental Analysis: C, 71.23; H, 4.54; N, 16.61; S, 7.61

Synonym:A8301; A 8301; A-8301

IUPAC/Chemical Name:3-(6-methylpyridin-2-yl)-N-phenyl-4-(quinolin-4-yl)-1H-pyrazole-1-carbothioamide

InChi Key:HIJMSZGHKQPPJS-UHFFFAOYSA-N

InChi Code:InChI=1S/C25H19N5S/c1-17-8-7-13-23(27-17)24-21(19-14-15-26-22-12-6-5-11-20(19)22)16-30(29-24)25(31)28-18-9-3-2-4-10-18/h2-16H,1H3,(H,28,31)

SMILES Code:S=C(N1N=C(C2=NC(C)=CC=C2)C(C3=CC=NC4=CC=CC=C34)=C1)NC5=CC=CC=C5

Technical Data

Appearance:
white solid powder

Purity:
>98% (or refer to the Certificate of Analysis)

Shipping Condition:
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition:
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility:
Soluble in DMSO, not in water

Shelf Life:
>2 years if stored properly

Drug Formulation:
This drug may be formulated in DMSO

Stock Solution Storage:
0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code:
2934.99.9001

Additional Information

References

1: Spinato S, Galindo-Moreno P, Zaffe D, BernardelloF, Soardi CM. Is socket healing conditioned by buccal plate thickness? Aclinical and histologic study 4 months after mineralized human boneallografting. Clin Oral Implants Res. 2012 Nov 21. doi:10.1111/clr.12073. [Epub ahead of print] PubMed PMID: 23167308.

2: Chen WP, Wu SM. Small molecule regulators of postnatal Nkx2.5cardiomyoblast proliferation and differentiation. J Cell Mol Med. 2012May;16(5):961-5. doi: 10.1111/j.1582-4934.2011.01513.x. PubMed PMID:22212626; PubMed Central PMCID: PMC3325363.

3: Shimada H, Hashimoto Y, Nakada A, Shigeno K, Nakamura T. Acceleratedgeneration of human induced pluripotent stem cells with retroviraltransduction and chemical inhibitors under physiological hypoxia.Biochem Biophys Res Commun. 2012 Jan 13;417(2):659-64. doi:10.1016/j.bbrc.2011.11.111. Epub 2011 Dec 8. PubMed PMID: 22172948.

4: Vogt J, Traynor R, Sapkota GP. The specificities of small moleculeinhibitors of the TGFß and BMP pathways. Cell Signal. 2011Nov;23(11):1831-42. doi: 10.1016/j.cellsig.2011.06.019. Epub 2011 Jun29. PubMed PMID: 21740966.

5: Yamamura S, Matsumura N, Mandai M, Huang Z, Oura T, Baba T, HamanishiJ, Yamaguchi K, Kang HS, Okamoto T, Abiko K, Mori S, Murphy SK, KonishiI. The activated transforming growth factor-beta signaling pathway inperitoneal metastases is a potential therapeutic target in ovariancancer. Int J Cancer. 2012 Jan 1;130(1):20-8. doi: 10.1002/ijc.25961.Epub 2011 Apr 18. PubMed PMID: 21503873.

6: Yuan X, Wan H, Zhao X, Zhu S, Zhou Q, Ding S. Brief report: combinedchemical treatment enables Oct4-induced reprogramming from mouseembryonic fibroblasts. Stem Cells. 2011 Mar;29(3):549-53. doi:10.1002/stem.594. PubMed PMID: 21425417.

7: Yu J, Chau KF, Vodyanik MA, Jiang J, Jiang Y. Efficient feeder-freeepisomal reprogramming with small molecules. PLoS One. 2011 Mar1;6(3):e17557. doi: 10.1371/journal.pone.0017557. PubMed PMID: 21390254;PubMed Central PMCID: PMC3046978.

8: Furutani Y, Umemoto T, Murakami M, Matsui T, Funaba M. Role ofendogenous TGF-β family in myogenic differentiation of C2C12 cells. JCell Biochem. 2011 Feb;112(2):614-24. doi: 10.1002/jcb.22953. PubMedPMID: 21268083.

9: Yuan X, Wan H, Zhao X, Zhu S, Zhou Q, Ding S. Combined ChemicalTreatment Enables Oct4-Induced Reprogramming from Mouse EmbryonicFibroblasts. Stem Cells. 2011 Jan 7. [Epub ahead of print] PubMed PMID:21218442.

10: Kawano K, Maitani Y. [Tumor permeability of nanocarriers observed bydynamic contrast-enhanced magnetic resonance imaging]. Yakugaku Zasshi.2010 Dec;130(12):1679-85. Review. Japanese. PubMed PMID: 21139395.

11: Taniguchi Y, Kawano K, Minowa T, Sugino T, Shimojo Y, Maitani Y.Enhanced antitumor efficacy of folate-linked liposomal doxorubicin withTGF-β type I receptor inhibitor. Cancer Sci. 2010 Oct;101(10):2207-13.doi: 10.1111/j.1349-7006.2010.01646.x. Epub 2010 Jul 1. PubMed PMID:20608940.

12: Minowa T, Kawano K, Kuribayashi H, Shiraishi K, Sugino T, Hattori Y,Yokoyama M, Maitani Y. Increase in tumour permeability followingTGF-beta type I receptor-inhibitor treatment observed by dynamiccontrast-enhanced MRI. Br J Cancer. 2009 Dec 1;101(11):1884-90. doi:10.1038/sj.bjc.6605367. Epub 2009 Nov 3. PubMed PMID: 19888220; PubMedCentral PMCID: PMC2788254.

13: Hoberg M, Rudert M, Pap T, Klein G, Gay S, Aicher WK. Attachment tolaminin-111 facilitates transforming growth factor beta-inducedexpression of matrix metalloproteinase-3 in synovial fibroblasts. AnnRheum Dis. 2007 Apr;66(4):446-51. Epub 2006 Nov 23. PubMed PMID:17124250; PubMed Central PMCID: PMC1856036.

14: Tojo M, Hamashima Y, Hanyu A, Kajimoto T, Saitoh M, Miyazono K, NodeM, Imamura T. The ALK-5 inhibitor A-83-01 inhibits Smad signaling andepithelial-to-mesenchymal transition by transforming growth factor-beta.Cancer Sci. 2005 Nov;96(11):791-800. PubMed PMID: 16271073.

品牌介绍
MedKoo 美帝药库公司以药物化学合成技术为核心,密切结合全球抗癌新药研发领域中的新技术、新理论、新趋势和新的发展方向,不断推出抗癌化合物新品种。 。 美帝药库MedKoo将在中国建立药物化学合成生产基地和多个现代化药物化合物存储仓库。 美帝药库的药物化合物来源于以下几个渠道:自主合成、委托化学合成、合作伙伴、和从国内外市场上选购。 MedKoo美帝药库的抗癌分子库 MedKoo的目标是打造全球规模最大、品种最多、类别最全和质量最好的小分子抗癌化合物库。MedKoo的抗癌药库将由下列5个分子库组成: (1)上市抗癌药库:该库将含有大约100个全球已批准上市的小分子抗癌化合物; (2)抗癌候选药物库:该分子库含有大约400个世界各国正在临床研究中抗癌小分子候选药物; (3)同系抗癌分子库:该分子库将含有多个化学结构类似或抗癌机制类似的分子包; (4)抗癌分子预制模块库:该库主要含有用于组建抗癌目标分子的分子模块包; (5)同位素标记抗癌分子库。