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商品详细MedKoo/MRK003/1/205885
MedKoo/MRK003/1/205885
MedKoo/MRK003/1/205885
商品编号: 205885
品牌: MedKoo
市场价: ¥0.00
美元价: 0.00
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

MRK003

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

MedKoo CAT#:205885

CAS#:623165-93-5

Description:MRK003 is a γ-secretase inhibitor exhibits promising in vitro pre-clinical activity in multiple myeloma and non-Hodgkin's lymphoma. MRK003 treatment induced caspase-dependent apoptosis and inhibited proliferation of MM and NHL cell lines and patient cells. Examination of signaling events after treatment showed time-dependent decrease in levels of the notch intracellular domain, Hes1 and c-Myc. MRK003 downregulated cyclin D1, Bcl-Xl and Xiap levels in NHL cells and p21, Bcl-2 and Bcl-Xl in MM cells. In addition, MRK003 caused an upregulation of pAkt, indicating crosstalk with the PI3K/Akt pathway.

Price and Availability

SizePriceShipping out timeQuantity
Inquire bulk and customized quantity

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

MRK003 is not in stock, but may be available through custom synthesis. For cost-effective reason, minimum 1 gram order is requested. The product will be characterized by NMR, HPLC and MS analysis. Purity (HPLC) is usually >98%. CoA, QC data, MSDS will be provided when product is successfully made. The estimated lead time is 2-3 months. Please send email to sales@medkoo.com to inquire quote.

Chemical Structure

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Theoretical Analysis

MedKoo Cat#: 205885Name: MRK003CAS#: 623165-93-5Chemical Formula: C25H31F6N3O2SExact Mass: 551.20412Molecular Weight: 551.59Elemental Analysis:C, 54.44; H, 5.66; F, 20.67; N, 7.62; O, 5.80; S, 5.81

Synonym:MRK003; MRK 003; MRK-003.

IUPAC/Chemical Name:(3'R,6R,9R)-5'-(2,2,2-trifluoroethyl)-2-((E)-3-(4-(trifluoromethyl)piperidin-1-yl)prop-1-en-1-yl)-5,6,7,8,9,10-hexahydrospiro[6,9-methanobenzo[8]annulene-11,3'-[1,2,5]thiadiazolidine] 1',1'-dioxide.

InChi Key:NKHUILHBYOOZDF-RWIQBJEJSA-N

InChi Code:InChI=1S/C25H31F6N3O2S/c26-24(27,28)16-34-15-23(32-37(34,35)36)21-5-6-22(23)14-19-12-17(3-4-18(19)13-21)2-1-9-33-10-7-20(8-11-33)25(29,30)31/h1-4,12,20-22,32H,5-11,13-16H2/b2-1+/t21-,22-,23-/m1/s1

SMILES Code:FC(C1CCN(C/C=C/C2=CC=C3C(C[C@@]4([H])CC[C@]([C@@]4(CN5CC(F)(F)F)NS5(=O)=O)([H])C3)=C2)CC1)(F)F

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

  Highlights of recent research using this agent MRK-003 inhibits Notch3 signaling, growth, and apoptosis of lung cancer cell lines in vitro and in vivo using mouse xenograft models  (Cancer Res 2007;67(17):8051–7, http://cancerres.aacrjournals.org/content/67/17/8051.full).   

References

1: Tanaka S, Nakada M, Yamada D, Nakano I, Todo T,Ino Y, Hoshii T, Tadokoro Y, Ohta K, Ali MA, Hayashi Y, Hamada J, HiraoA. Strong therapeutic potential of γ-secretase inhibitor MRK003 forCD44-high and CD133-low glioblastoma initiating cells. J Neurooncol.2015 Jan;121(2):239-50. doi: 10.1007/s11060-014-1630-z. Epub 2014 Oct 8.PubMed PMID: 25293440.

2: Stoeck A, Lejnine S, Truong A, Pan L, Wang H, Zang C, Yuan J, Ware C,MacLean J, Garrett-Engele PW, Kluk M, Laskey J, Haines BB, Moskaluk C,Zawel L, Fawell S, Gilliland G, Zhang T, Kremer BE, Knoechel B,Bernstein BE, Pear WS, Liu XS, Aster JC, Sathyanarayanan S. Discovery ofbiomarkers predictive of GSI response in triple-negative breast cancerand adenoid cystic carcinoma. Cancer Discov. 2014 Oct;4(10):1154-67. doi:10.1158/2159-8290.CD-13-0830. Epub 2014 Aug 7. PubMed PMID: 25104330;PubMed Central PMCID: PMC4184927.

3: Groeneweg JW, DiGloria CM, Yuan J, Richardson WS, Growdon WB,Sathyanarayanan S, Foster R, Rueda BR. Inhibition of notch signaling incombination with Paclitaxel reduces platinum-resistant ovarian tumorgrowth. Front Oncol. 2014 Jul 7;4:171. doi: 10.3389/fonc.2014.00171.eCollection 2014. PubMed PMID: 25072022; PubMed Central PMCID:PMC4083224.

4: Samore WR, Gondi CS. Brief overview of selected approaches intargeting pancreatic adenocarcinoma. Expert Opin Investig Drugs. 2014Jun;23(6):793-807. doi: 10.1517/13543784.2014.902933. Epub 2014 Mar 27.Review. PubMed PMID: 24673265.

5: Groeneweg JW, Hall TR, Zhang L, Kim M, Byron VF, Tambouret R,Sathayanrayanan S, Foster R, Rueda BR, Growdon WB. Inhibition of gamma-secretaseactivity impedes uterine serous carcinoma growth in a human xenograftmodel. Gynecol Oncol. 2014 Jun;133(3):607-15. doi:10.1016/j.ygyno.2014.03.560. Epub 2014 Mar 22. PubMed PMID: 24667249.

6: Liu QQ, Liu JL, Guo DM, Teng QL. [Inhibitory effects of gammasecretase inhibitor on human multiple myeloma xenograft mouse model].Zhonghua Xue Ye Xue Za Zhi. 2013 Sep;34(9):794-7. doi:10.3760/cma.j.issn.0253-2727.2013.09.012. Chinese. PubMed PMID:24103879.

7: Timme CR, Gruidl M, Yeatman TJ. Gamma-secretase inhibition attenuatesoxaliplatin-induced apoptosis through increased Mcl-1 and/or Bcl-xL inhuman colon cancer cells. Apoptosis. 2013 Oct;18(10):1163-74. doi:10.1007/s10495-013-0883-x. PubMed PMID: 23887890.

8: Chu Q, Orr BA, Semenkow S, Bar EE, Eberhart CG. Prolonged inhibitionof glioblastoma xenograft initiation and clonogenic growth following invivo Notch blockade. Clin Cancer Res. 2013 Jun 15;19(12):3224-33. doi:10.1158/1078-0432.CCR-12-2119. Epub 2013 Apr 29. PubMed PMID: 23630166;PubMed Central PMCID: PMC3686970.

9: Hassan KA, Wang L, Korkaya H, Chen G, Maillard I, Beer DG,Kalemkerian GP, Wicha MS. Notch pathway activity identifies cells withcancer stem cell-like properties and correlates with worse survival inlung adenocarcinoma. Clin Cancer Res. 2013 Apr 15;19(8):1972-80. doi:10.1158/1078-0432.CCR-12-0370. Epub 2013 Feb 26. PubMed PMID: 23444212;PubMed Central PMCID: PMC3630232.

10: Jin R, Nakada M, Teng L, Furuta T, Sabit H, Hayashi Y, Demuth T,Hirao A, Sato H, Zhao G, Hamada J. Combination therapy using Notch andAkt inhibitors is effective for suppressing invasion but notproliferation in glioma cells. Neurosci Lett. 2013 Feb 8;534:316-21. doi:10.1016/j.neulet.2012.12.008. Epub 2012 Dec 20. PubMed PMID: 23262078.

11: Liang S, Galluzzo P, Sobol A, Skucha S, Rambo B, Bocchetta M.Multimodality Approaches to Treat Hypoxic Non-Small Cell Lung Cancer(NSCLC) Microenvironment. Genes Cancer. 2012 Feb;3(2):141-51. doi:10.1177/1947601912457025. PubMed PMID: 23050046; PubMed Central PMCID:PMC3463922.

12: Mizuma M, Rasheed ZA, Yabuuchi S, Omura N, Campbell NR, de Wilde RF,De Oliveira E, Zhang Q, Puig O, Matsui W, Hidalgo M, Maitra A,Rajeshkumar NV. The gamma secretase inhibitor MRK-003 attenuatespancreatic cancer growth in preclinical models. Mol Cancer Ther. 2012Sep;11(9):1999-2009. doi: 10.1158/1535-7163.MCT-12-0017. Epub 2012 Jul2. PubMed PMID: 22752426; PubMed Central PMCID: PMC3438318.

13: Cook N, Frese KK, Bapiro TE, Jacobetz MA, Gopinathan A, Miller JL,Rao SS, Demuth T, Howat WJ, Jodrell DI, Tuveson DA. Gamma secretaseinhibition promotes hypoxic necrosis in mouse pancreatic ductaladenocarcinoma. J Exp Med. 2012 Mar 12;209(3):437-44. doi:10.1084/jem.20111923. Epub 2012 Feb 20. PubMed PMID: 22351932; PubMedCentral PMCID: PMC3302221.

14: Asnaghi L, Ebrahimi KB, Schreck KC, Bar EE, Coonfield ML, Bell WR,Handa J, Merbs SL, Harbour JW, Eberhart CG. Notch signaling promotesgrowth and invasion in uveal melanoma. Clin Cancer Res. 2012 Feb1;18(3):654-65. doi: 10.1158/1078-0432.CCR-11-1406. Epub 2012 Jan 6.PubMed PMID: 22228632.

15: Osanyingbemi-Obidi J, Dobromilskaya I, Illei PB, Hann CL, Rudin CM.Notch signaling contributes to lung cancer clonogenic capacity in vitrobut may be circumvented in tumorigenesis in vivo. Mol Cancer Res. 2011Dec;9(12):1746-54. doi: 10.1158/1541-7786.MCR-11-0286. Epub 2011 Oct 12.PubMed PMID: 21994468; PubMed Central PMCID: PMC3243765.

16: Pandya K, Meeke K, Clementz AG, Rogowski A, Roberts J, Miele L,Albain KS, Osipo C. Targeting both Notch and ErbB-2 signalling pathwaysis required for prevention of ErbB-2-positive breast tumour recurrence.Br J Cancer. 2011 Sep 6;105(6):796-806. doi: 10.1038/bjc.2011.321. Epub2011 Aug 16. PubMed PMID: 21847123; PubMed Central PMCID: PMC3171020.

17: Ramakrishnan V, Ansell S, Haug J, Grote D, Kimlinger T, Stenson M,Timm M, Wellik L, Halling T, Rajkumar SV, Kumar S. MRK003, a γ-secretaseinhibitor exhibits promising in vitro pre-clinical activity in multiplemyeloma and non-Hodgkin"s lymphoma. Leukemia. 2012 Feb;26(2):340-8. doi:10.1038/leu.2011.192. Epub 2011 Aug 9. PubMed PMID: 21826062.

18: Lin H, Xiong W, Zhang X, Liu B, Zhang W, Zhang Y, Cheng J, Huang H.Notch-1 activation-dependent p53 restoration contributes to resveratrol-inducedapoptosis in glioblastoma cells. Oncol Rep. 2011 Oct;26(4):925-30. doi:10.3892/or.2011.1380. Epub 2011 Jul 4. PubMed PMID: 21743969.

19: Clementz AG, Rogowski A, Pandya K, Miele L, Osipo C. NOTCH-1 andNOTCH-4 are novel gene targets of PEA3 in breast cancer: noveltherapeutic implications. Breast Cancer Res. 2011 Jun 14;13(3):R63. doi:10.1186/bcr2900. PubMed PMID: 21679465; PubMed Central PMCID:PMC3218952.

20: Cao L, Zhou Y, Zhai B, Liao J, Xu W, Zhang R, Li J, Zhang Y, Chen L,Qian H, Wu M, Yin Z. Sphere-forming cell subpopulations with cancer stemcell properties in human hepatoma cell lines. BMC Gastroenterol. 2011Jun 14;11:71. doi: 10.1186/1471-230X-11-71. PubMed PMID: 21669008;PubMed Central PMCID: PMC3136412.

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。