Home > Products > Pharmaceuticals & Life Science > Pharmaceutical Intermediates > N-(3-(5-(4-Chlorophenyl)-1H-pyrrolo[2,3-B]pyridine-3-carbonyl)-2,4-difluorophenyl)propane-1-sulfonaMide
N-(3-(5-(4-Chlorophenyl)-1H-pyrrolo[2,3-B]pyridine-3-carbonyl)-2,4-difluorophenyl)propane-1-sulfonaMide structure, CAS 918504-65-1

N-(3-(5-(4-Chlorophenyl)-1H-pyrrolo[2,3-B]pyridine-3-carbonyl)-2,4-difluorophenyl)propane-1-sulfonaMide

CAS Number918504-65-1

SynonymsZelboraf; Vemurafenib (PLX4032,RG7204); PLX4032

Molecular FormulaC23H18O3N3Cl1S1F2

Molecular Weight489.93

Purity

Density1.5±0.1 g/cm3

Boiling Point711.4±70.0 °C at 760 mmHg

Melting Point260-262 °C

Flash Point

Appearance

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Cat. No.: 2A-2176606 Purity:
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Quality Control of [ 918504-65-1 ] SDS Specification MoL

Chemical & Physical Properties
CAS Number918504-65-1
Catalog No.2A-2176606
Chinese Name维罗非尼
SynonymsZelboraf; Vemurafenib (PLX4032,RG7204); PLX4032
Molecular FormulaC23H18O3N3Cl1S1F2
Molecular Weight489.93
Density1.5±0.1 g/cm3
Boiling Point711.4±70.0 °C at 760 mmHg
Melting Point260-262 °C
Storage Condition-20°C
ApplicationVemurafenib is a potent B-RAF inhibitor that inhibits the activity of RAFV600E and c-RAF-1 with IC50 of 31 nM and 48 nM, respectively.
HTC2935009090
MDL NumberMFCD18074504
SMILESCCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(-c4ccc(Cl)cc4)cc23)c1F
InChI KeyGPXBXXGIAQBQNI-UHFFFAOYSA-N
MSDSmsds/177133_1_918504_65_1.pdf
Use ofVemurafenib is a novel and potent inhibitor of B-RAF kinase, with IC50s of 31 and 48 nM for RAFV600E and c-RAF-1, respectively. Properties Name vemurafenib Synonym More Synonyms Vemurafenib (PLX4032) Biological Activity Description Vemurafenib is a novel and potent inhibitor of B-RAF kinase, with IC50s of 31 and 48 nM for RAFV600E and c-RAF-1, respectively. Related Catalog Signaling Pathways >> Autophagy >> Autophagy Signaling Pathways >> MAPK/ERK Pathway >> Raf Research Areas >> Cancer B-RafV600E:31 nM (IC50) c-Raf-1:48 nM (IC50) References [1]. Bollag G, et al. Clinical efficacy of a RAF inhibitor needs broad target blockade in BRAF-mutant melanoma. Nature, 2010, 467(7315), 596-599. [2]. Yang H, et al. RG7204 (PLX4032), a selective BRAFV600E inhibitor, displays potent antitumor activity in preclinical melanoma models. Cancer Res, 2010, 70(13), 5518-5527. [3]. Prahallad A, et al. Unresponsiveness of colon cancer to BRAF(V600E) inhibition through feedback activation of EGFR. Nature, 2012, 483(7387), 100-103. Chemical & Physical Properties Exact Mass 489.072540 PSA 100.30000 Index of Refraction 1.653 InChIKey GPXBXXGIAQBQNI-UHFFFAOYSA-N Safety Information HS Code 2935009090
Tax Rebate9.0%
SupervisionNone MFN tariff: 6.5% Ordinary tariff: 35.0%
Transport InfoProduct name: Summary 2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0%
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