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商品详细MedKoo/Amuvatinib/25mg/201950
MedKoo/Amuvatinib/25mg/201950
MedKoo/Amuvatinib/25mg/201950
商品编号: 201950
品牌: MedKoo
市场价: ¥3000.00
美元价: 1800.00
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

Amuvatinib
featured

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

MedKoo CAT#:201950

CAS#:850879-09-3 (free)

Description:Amuvatinib, also known as MP-470, is an orally bioavailable synthetic carbothioamide with potential antineoplastic activity. Multitargeted receptor tyrosine kinase inhibitor MP470 binds to mutant forms of the stem cell factor receptor (c-Kit; SCFR), inhibiting clinically relevant mutants of this receptor tyrosine kinase that may be associated with resistance to therapy. In addition, MP470 inhibits activities of other receptor tyrosine kinases, such as c-Met, Ret oncoprotein, and mutant forms of Flt3 and PDGFR alpha, which are frequently dysregulated in variety of tumors.

Price and Availability

SizePriceShipping out timeQuantity
25mgUSD 1502 Weeks
50mgUSD 2502 Weeks
100mgUSD 4502 Weeks
250mgUSD 9502 Weeks
500mgUSD 16502 Weeks
1gUSD 26502 Weeks
2gUSD 42502 Weeks
Inquire bulk and customized quantity

Pricing updated 2021-01-23.Prices are subject to change without notice.

Amuvatinib (MP470), 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#: 201950Name: AmuvatinibCAS#: 850879-09-3 (free)Chemical Formula: C23H21N5O3SExact Mass: 447.13651Molecular Weight: 447.51Elemental Analysis:C, 61.73; H, 4.73; N, 15.65; O, 10.73; S, 7.17

Related CAS #:850879-09-3 (free); 1055986-67-8 (hydrochloride)

Synonym:HPK 56; HPK-56; HPK56; MP470; MP-470; MP 470; Amuvatinib.

IUPAC/Chemical Name:N-(benzo[d][1,3]dioxol-5-ylmethyl)-4-(benzofuro[3,2-d]pyrimidin-4-yl)piperazine-1-carbothioamide.

InChi Key:FOFDIMHVKGYHRU-UHFFFAOYSA-N

InChi Code:InChI=1S/C23H21N5O3S/c32-23(24-12-15-5-6-18-19(11-15)30-14-29-18)28-9-7-27(8-10-28)22-21-20(25-13-26-22)16-3-1-2-4-17(16)31-21/h1-6,11,13H,7-10,12,14H2,(H,24,32)

SMILES Code:S=C(N1CCN(C2=C(OC3=CC=CC=C34)C4=NC=N2)CC1)NCC5=CC=C(OCO6)C6=C5

Technical Data

Appearance:
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

According to news published on 15 Apr 2008;  Research data build upon previous results showing that MP-470 exhibits anti-tumor activity in breast and prostate cancer cells. The fact that MP-470 in combination with erlotinib effectively suppressed the HER pathway suggests that concurrent administration of both compounds could represent a new treatment for prostate and breast cancers.According to news published on;  Research    

References

1: Phillip CJ, Zaman S, Shentu S, Balakrishnan K,Zhang J, Baladandayuthapani V, Taverna P, Redkar S, Wang M, StellrechtCM, Gandhi V. Targeting MET kinase with the small-molecule inhibitoramuvatinib induces cytotoxicity in primary myeloma cells and cell lines.J Hematol Oncol. 2013 Dec 10;6:92. doi: 10.1186/1756-8722-6-92. PubMedPMID: 24326130; PubMed Central PMCID: PMC3878866.

2: Asiedu MK, Beauchamp-Perez FD, Ingle JN, Behrens MD, Radisky DC,Knutson KL. AXL induces epithelial-to-mesenchymal transition andregulates the function of breast cancer stem cells. Oncogene. 2014 Mar6;33(10):1316-24. doi: 10.1038/onc.2013.57. Epub 2013 Mar 11. PubMedPMID: 23474758; PubMed Central PMCID: PMC3994701.

3: Tibes R, Fine G, Choy G, Redkar S, Taverna P, Oganesian A, Sahai A,Azab M, Tolcher AW. A phase I, first-in-human dose-escalation study ofamuvatinib, a multi-targeted tyrosine kinase inhibitor, in patients withadvanced solid tumors. Cancer Chemother Pharmacol. 2013Feb;71(2):463-71. doi: 10.1007/s00280-012-2019-3. Epub 2012 Nov 23.PubMed PMID: 23178951.

4: Gujral TS, Karp RL, Finski A, Chan M, Schwartz PE, MacBeath G, SorgerP. Profiling phospho-signaling networks in breast cancer usingreverse-phase protein arrays. Oncogene. 2013 Jul 18;32(29):3470-6. doi:10.1038/onc.2012.378. Epub 2012 Sep 3. PubMed PMID: 22945653; PubMedCentral PMCID: PMC3670968.

5: Choy G, Joshi-Hangal R, Oganesian A, Fine G, Rasmussen S, Collier J,Kissling J, Sahai A, Azab M, Redkar S. Safety, tolerability, andpharmacokinetics of amuvatinib from three phase 1 clinical studies inhealthy volunteers. Cancer Chemother Pharmacol. 2012 Jul;70(1):183-90.doi: 10.1007/s00280-012-1821-2. Epub 2012 Feb 15. PubMed PMID: 22349808.

6: Zhao H, Luoto KR, Meng AX, Bristow RG. The receptor tyrosine kinaseinhibitor amuvatinib (MP470) sensitizes tumor cells to radio- andchemo-therapies in part by inhibiting homologous recombination.Radiother Oncol. 2011 Oct;101(1):59-65. doi:10.1016/j.radonc.2011.08.013. Epub 2011 Sep 6. PubMed PMID: 21903282.

7: Baxter PA, Thompson PA, McGuffey LM, Gibson BW, Dauser RC, NuchternJG, Shi C, Inloes R, Choy G, Redkar S, Blaney SM. Plasma andcerebrospinal fluid pharmacokinetics of MP470 in non-human primates.Cancer Chemother Pharmacol. 2011 Apr;67(4):809-12. doi:10.1007/s00280-010-1380-3. Epub 2010 Jun 19. PubMed PMID: 20563581.

8: Welsh JW, Mahadevan D, Ellsworth R, Cooke L, Bearss D, Stea B. Thec-Met receptor tyrosine kinase inhibitor MP470 radiosensitizesglioblastoma cells. Radiat Oncol. 2009 Dec 22;4:69. doi:10.1186/1748-717X-4-69. PubMed PMID: 20028557; PubMed Central PMCID:PMC2806296.

9: Qi W, Cooke LS, Stejskal A, Riley C, Croce KD, Saldanha JW, Bearss D,Mahadevan D. MP470, a novel receptor tyrosine kinase inhibitor, incombination with Erlotinib inhibits the HER family/PI3K/Akt pathway andtumor growth in prostate cancer. BMC Cancer. 2009 May 11;9:142. doi:10.1186/1471-2407-9-142. PubMed PMID: 19432987; PubMed Central PMCID:PMC2685437.

10: Mahadevan D, Cooke L, Riley C, Swart R, Simons B, Della Croce K,Wisner L, Iorio M, Shakalya K, Garewal H, Nagle R, Bearss D. A noveltyrosine kinase switch is a mechanism of imatinib resistance ingastrointestinal stromal tumors. Oncogene. 2007 Jun 7;26(27):3909-19.Epub 2007 Feb 26. PubMed PMID: 17325667.

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。