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MedKoo/Obatoclax mesylatefeatured/10mg/202050

价格
¥3000.00
货号:202050
浏览量:96
品牌:MedKoo
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商品描述

Obatoclax mesylate
featured

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

MedKoo CAT#:202050

CAS#:803712-79-0 (mesylate)

Description:Obatoclax, also known as GX 015-070, a synthetic small-molecule inhibitor of the bcl-2 family of proteins with potential pro-apoptotic and antineoplastic activities. Obatoclax binds to members of the Bcl-2 protein family, preventing the binding of these anti-apoptotic proteins to the pro-apoptotic proteins Bax and Bak and so promoting the activation of the apoptotic pathway in Bcl-2-overexpressing cells. The Bcl-2 family of proteins (bcl-2, bcl-xl, bcl-w, and Mcl-1) are overexpressed in a wide variety of cancers, including those of the lymphatic system, breast, lung, prostate, and colon.

Price and Availability

SizePriceShipping out timeQuantity
10mgUSD 1502 Weeks
25mgUSD 2502 Weeks
50mgUSD 4502 Weeks
100mgUSD 7502 Weeks
200mgUSD 12502 Weeks
500mgUSD 19502 Weeks
1gUSD 27502 Weeks
2gUSD 42502 Weeks
Inquire bulk and customized quantity

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

Obatoclax mesylate, 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#: 202050Name: Obatoclax mesylateCAS#: 803712-79-0 (mesylate)Chemical Formula: C21H23N3O4SExact Mass: 317.15281Molecular Weight: 413.49002Elemental Analysis: C, 61.00; H, 5.61; N, 10.16; O, 15.48; S, 7.75

Related CAS #:803712-67-6 (free base)803712-79-0 (mesylate)

Synonym:Obatoclax; Obatoclax mesylate; GX 015-070; GX015-070; GX-015-070; GX 015070; GX015070; GX-015070; GX 05-070; GX15070MS.

IUPAC/Chemical Name:(Z)-2-(2-((3,5-dimethyl-1H-pyrrol-2-yl)methylene)-3-methoxy-2H-pyrrol-5-yl)-1H-indole methanesulfonate

InChi Key:ZFKXDVMHNXPEIY-PEZBNFGJSA-N

InChi Code:InChI=1S/C20H19N3O.CH4O3S/c1-12-8-13(2)21-16(12)10-19-20(24-3)11-18(23-19)17-9-14-6-4-5-7-15(14)22-17;1-5(2,3)4/h4-11,21-22H,1-3H3;1H3,(H,2,3,4)/b19-10-;

SMILES Code:COC1=CC(C(N2)=CC3=C2C=CC=C3)=N/C1=CC4=C(C)C=C(C)N4.CS(=O)(O)=O

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:
>5 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

Related CAS#803712-67-6 (Obatoclax free base)803712-79-0(Obatoclax mesylate) 

References

1: Díaz de Greñu B, Hernández PI, Espona M, QuiñoneroD, Light ME, Torroba T, Pérez-Tomás R, Quesada R. Synthetic ProdiginineObatoclax (GX15-070) and Related Analogues: Anion Binding, TransmembraneTransport, and Cytotoxicity Properties. Chemistry. 2011 Nov 9. doi:10.1002/chem.201101547. [Epub ahead of print] PubMed PMID: 22069220.

2: Lieber J, Ellerkamp V, Wenz J, Kirchner B, Warmann SW, Fuchs J,Armeanu-Ebinger S. Apoptosis sensitizers enhance cytotoxicity inhepatoblastoma cells. Pediatr Surg Int. 2011 Oct 5. [Epub ahead ofprint] PubMed PMID: 21971946.

3: Martínez-Paniagua MA, Baritaki S, Huerta-Yepez S, Ortiz-Navarrete VF,González-Bonilla C, Bonavida B, Vega MI. Mcl-1 and YY1 inhibition andinduction of DR5 by the BH3-mimetic Obatoclax (GX15-070) contribute inthe sensitization of B-NHL cells to TRAIL apoptosis. Cell Cycle. 2011Aug 15;10(16):2792-805. Epub 2011 Aug 15. PubMed PMID: 21822052.

4: Jóna A, Khaskhely N, Buglio D, Shafer JA, Derenzini E, Bollard CM,Medeiros LJ, Illés A, Ji Y, Younes A. The histone deacetylase inhibitorentinostat (SNDX-275) induces apoptosis in Hodgkin lymphoma cells andsynergizes with Bcl-2 family inhibitors. Exp Hematol. 2011Oct;39(10):1007-1017.e1. doi: 10.1016/j.exphem.2011.07.002. Epub 2011Jul 20. PubMed PMID: 21767511; PubMed Central PMCID: PMC3177003.

5: Acoca S, Cui Q, Shore GC, Purisima EO. Molecular dynamics study ofsmall molecule inhibitors of the Bcl-2 family. Proteins. 2011Sep;79(9):2624-36. doi: 10.1002/prot.23083. Epub 2011 Jun 30. PubMedPMID: 21721047.

6: Herishanu Y, Gibellini F, Njuguna N, Hazan-Halevy I, Farooqui M, BernS, Keyvanfar K, Lee E, Wilson W, Wiestner A. Activation of CD44, areceptor for extracellular matrix components, protects chroniclymphocytic leukemia cells from spontaneous and drug induced apoptosisthrough MCL-1. Leuk Lymphoma. 2011 Sep;52(9):1758-69. Epub 2011 Jun 8.PubMed PMID: 21649540.

7: Paik PK, Rudin CM, Pietanza MC, Brown A, Rizvi NA, Takebe N, TravisW, James L, Ginsberg MS, Juergens R, Markus S, Tyson L, Subzwari S, KrisMG, Krug LM. A phase II study of obatoclax mesylate, a Bcl-2 antagonist,plus topotecan in relapsed small cell lung cancer. Lung Cancer. 2011Dec;74(3):481-5. Epub 2011 May 26. PubMed PMID: 21620511.

8: Brem EA, Thudium K, Khubchandani S, Tsai PC, Olejniczak SH, Bhat S,Riaz W, Gu J, Iqbal A, Campagna R, Knight J, Mavis C, Hoskin P, Deeb G,Gibbs JF, Fetterly G, Czuczman MS, Hernandez-Ilizaliturri FJ. Distinctcellular and therapeutic effects of obatoclax in rituximab-sensitive and-resistant lymphomas. Br J Haematol. 2011 Jun;153(5):599-611. doi:10.1111/j.1365-2141.2011.08669.x. Epub 2011 Apr 15. PubMed PMID:21492126; PubMed Central PMCID: PMC3092002.

9: Dean EJ, Cummings J, Roulston A, Berger M, Ranson M, Blackhall F,Dive C. Optimization of circulating biomarkers of obatoclax-induced celldeath in patients with small cell lung cancer. Neoplasia. 2011Apr;13(4):339-47. PubMed PMID: 21472138; PubMed Central PMCID:PMC3071082.

10: Heidari N, Hicks MA, Harada H. GX15-070 (obatoclax) overcomesglucocorticoid resistance in acute lymphoblastic leukemia throughinduction of apoptosis and autophagy. Cell Death Dis. 2010 Sep 16;1:e76.PubMed PMID: 21364679; PubMed Central PMCID: PMC3032343.

我国旅美科学家陈清奇博士创立的MedKoo美帝药库医药公司目前正在建立全球第一个小分子抗癌药库。 MedKoo是一家以研发、生产和销售小分子抗癌化合物为主的医药科技公司。 业务范围 为全球所有从事抗癌药物研究和开发的制药公司,高校,研究院所,政府相关机构提供与抗癌药物分子相关的产品、试剂和技术服务。 技术核心 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。 建造目标 MedKoo美帝药库的目标是:建成全球最大的小分子抗癌药库 ,品种最多最全、质量最好最可靠。美帝药库的宗旨是:客户第一;质量第一;信誉第一;创新第一。