请使用支持JavaScript的浏览器!
主营:抗癌化学试剂和激酶抑制剂
℡ 4000-520-616
℡ 4000-520-616
MedKoo/LFM-A13newfeatured/50mg/401531
产品编号:401531
市  场 价:¥3000.00
场      地:美国(厂家直采)
产品分类: 蛋白类>多肽>多肽合成>
联系QQ:1570468124
电话号码:4000-520-616
邮      箱: info@ebiomall.com
美  元  价:$150.00
品      牌: MedKoo
公      司:MedKoo Biosciences, Inc
公司分类:
MedKoo/LFM-A13newfeatured/50mg/401531
商品介绍

LFM-A13
new
featured

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

MedKoo CAT#:401531

CAS#:244240-24-2

Description:LFM-A13 is a potent and selective inhibitor of Bruton's tyrosine kinase (BTK). LFM-A13 may be useful as a new class of chemosensitizing and apoptosis-promoting antileukemic agents for treatment of patients with chemotherapy-resistant B-lineage leukemias or lymphomas.

Price and Availability

SizePriceShipping out timeQuantity
50mgUSD 1502 Weeks
100mgUSD 2502 Weeks
200mgUSD 4502 Weeks
500mgUSD 8502 Weeks
1gUSD 14502 Weeks
2gUSD 19502 Weeks
5gUSD 32502 Weeks
10gUSD 49502 Weeks
Inquire bulk and customized quantity

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

LFM-A13, 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

img

Theoretical Analysis

MedKoo Cat#: 401531Name: LFM-A13CAS#: 244240-24-2Chemical Formula: C11H8Br2N2O2Exact Mass: 357.89525Molecular Weight: 360.0Elemental Analysis: C, 36.70; H, 2.24; Br, 44.39; N, 7.78; O, 8.89

Synonym:LFM A13; LFM-A13; LFM A13

IUPAC/Chemical Name:2-Cyano-N-(2,5-dibromophenyl)-3-hydroxy-2-butenamide

InChi Key:UVSVTDVJQAJIFG-VURMDHGXSA-N

InChi Code:InChI=1S/C11H8Br2N2O2/c1-6(16)8(5-14)11(17)15-10-4-7(12)2-3-9(10)13/h2-4,16H,1H3,(H,15,17)/b8-6-

SMILES Code:C/C(O)=C(C#N)/C(NC1=CC(Br)=CC=C1Br)=O

Technical Data

Appearance:
Solid powder

Purity:
>98%

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

References

1: Uckun F, Dibirdik I, Sarkissian A, Qazi S. Invitro and in vivo chemosensitizing activity of LFM-A13, a dual-functioninhibitor of Bruton"s tyrosine kinase and polo-like kinases, againsthuman leukemic B-cell precursors. Arzneimittelforschung.2011;61(4):252-9. doi: 10.1055/s-0031-1296196. PubMed PMID: 21650085.

2: Uckun FM. Chemosensitizing anti-cancer activity of LFM-A13, aleflunomide metabolite analog targeting polo-like kinases. Cell Cycle.2007 Dec 15;6(24):3021-6. Epub 2007 Sep 26. PubMed PMID: 18073537.

3: DuMez D, Venkatachalam TK, Uckun FM. Large-scale synthesis of GMPgrade alpha-cyano-beta-hydroxy-beta-methyl-N-(2,5-dibromophenyl)propenamide (LFM-A13), a new anti-cancer drug candidate.Arzneimittelforschung. 2007;57(3):155-63. PubMed PMID: 17469650.

4: Uckun FM, Tibbles H, Venkatachalam T, DuMez D, Erbeck D. Preclinicaltoxicity and pharmacokinetics of the Bruton"s tyrosine kinase-targetinganti-leukemic drug candidate, alpha-cyano-beta-hydroxy-beta-methyl-N-(2,5-dibromophenyl) propenamide (LFM-A13). Arzneimittelforschung.2007;57(1):31-46. PubMed PMID: 17341007.

5: Uckun FM, Dibirdik I, Qazi S, Vassilev A, Ma H, Mao C, Benyumov A,Emami KH. Anti-breast cancer activity of LFM-A13, a potent inhibitor ofPolo-like kinase (PLK). Bioorg Med Chem. 2007 Jan 15;15(2):800-14. Epub2006 Oct 26. PubMed PMID: 17098432.

6: Tibbles HE, Samuel P, Erbeck D, Mahajan S, Uckun FM. In vivo toxicityand antithrombotic profile of the oral formulation of the antileukemicagent, LFM-A13-F. Arzneimittelforschung. 2004;54(6):330-9. PubMed PMID:15281619.

7: van den Akker E, van Dijk TB, Schmidt U, Felida L, Beug H, LöwenbergB, von Lindern M. The Btk inhibitor LFM-A13 is a potent inhibitor ofJak2 kinase activity. Biol Chem. 2004 May;385(5):409-13. PubMed PMID:15196000.

8: Uckun FM, Vassilev A, Bartell S, Zheng Y, Mahajan S, Tibbles HE. Theanti-leukemic Bruton"s tyrosine kinase inhibitor alpha-cyano-beta-hydroxy-beta-methyl-N-(2,5-dibromophenyl)propenamide (LFM-A13) prevents fatal thromboembolism. Leuk Lymphoma.2003 Sep;44(9):1569-77. PubMed PMID: 14565661.

9: Gilbert C, Levasseur S, Desaulniers P, Dusseault AA, Thibault N,Bourgoin SG, Naccache PH. Chemotactic factor-induced recruitment andactivation of Tec family kinases in human neutrophils. II. Effects ofLFM-A13, a specific Btk inhibitor. J Immunol. 2003 May15;170(10):5235-43. PubMed PMID: 12734372.

10: Uckun FM, Zheng Y, Cetkovic-Cvrlje M, Vassilev A, Lisowski E,Waurzyniak B, Chen H, Carpenter R, Chen CL. In vivo pharmacokineticfeatures, toxicity profile, and chemosensitizing activity of alpha-cyano-beta-hydroxy-beta-methyl-N-(2,5-dibromophenyl)propenamide (LFM-A13), a novel antileukemicagent targeting Bruton"s tyrosine kinase. Clin Cancer Res. 2002May;8(5):1224-33. PubMed PMID: 12006542.

11: Mahajan S, Ghosh S, Sudbeck EA, Zheng Y, Downs S, Hupke M, Uckun FM.Rational design and synthesis of a novel anti-leukemic agent targetingBruton"s tyrosine kinase (BTK), LFM-A13 [alpha-cyano-beta-hydroxy-beta-methyl-N-(2,5-dibromophenyl)propenamide]. J Biol Chem. 1999 Apr 2;274(14):9587-99.PubMed PMID: 10092645.

品牌介绍
MedKoo,由化学家和药学家陈清奇博士。北卡罗莱纳州的研究三角区(Research Triangle Park, 简称 RTP ),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,该公司的业务范围主要是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。
中文名MedKoo中    文美帝药库医药科技公司创立于2008年总部位于美国东海岸
自营商城图标
厂家直采
全球直采 正品优价
正品保障图标
正品保障
厂家直发 有线跟踪
解放采购图标
正规清关
CIF100%正规报关,提供发票
及时交付图标
及时交付
限时必达 不达必赔