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维罗非尼(PLX4032,RG7204)

规格或纯度: ≥98%
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货号 (SKU) 包装规格 是否现货 价格 数量
V127521-10mg 10mg 现货 Stock Image
V127521-25mg 25mg 现货 Stock Image
V127521-50mg 50mg 现货 Stock Image
V127521-100mg 100mg 现货 Stock Image
V127521-500mg 500mg 现货 Stock Image
V127521-1g 1g 现货 Stock Image
V127521-5g 5g 现货 Stock Image

基本描述

规格或纯度 ≥98%
英文名称 Vemurafenib (PLX4032, RG7204)
别名 维罗非尼
英文别名 PLX-4032; RG7204; R7204; RO5185426; PLX4032;N-[3-[[5-(4-Chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]carbonyl]-2,4-difluorophenyl]-1-propanesulfonamide
生化机理 Vemurafenib is a novel and potent inhibitor of B-RAFV600E with IC50 of 31 nM. Has been shown to kill melanoma cells in vitro.
储存温度 -20°C储存
运输条件 超低温冰袋运输
产品介绍

Vemurafenib (PLX4032, RG7204)是一种新型有效的B-Raf V600E抑制剂,IC50为31 nM。A novel and potent inhibitor of B-RAFV600E with IC50 of 31 nM.

Vemurafenib (PLX4032, RG7204) is a novel and potent inhibitor of B-Raf V600E with IC50 of 31 nM.
A novel and potent inhibitor of B-RAFV600E with IC50 of 31 nM.

名称和标识符

IUPAC Name N-[3-[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluorophenyl]propane-1-sulfonamide
INCHI InChI=1S/C23H18ClF2N3O3S/c1-2-9-33(31,32)29-19-8-7-18(25)20(21(19)26)22(30)17-12-28-23-16(17)10-14(11-27-23)13-3-5-15(24)6-4-13/h3-8,10-12,29H,2,9H2,1H3,(H,27,28)
InChi Key GPXBXXGIAQBQNI-UHFFFAOYSA-N
Canonical SMILES CCCS(=O)(=O)NC1=C(C(=C(C=C1)F)C(=O)C2=CNC3=C2C=C(C=N3)C4=CC=C(C=C4)Cl)F
分子式

C23H18ClF2N3O3S

PubChem CID 42611257
分子量 489.92

化学和物理性质

溶解性 Soluble in DMSO (100 mg/mL), and methanol. Insoluble in ethanol, and water
熔点 260-262°C

安全信息

象形图
ghs08

Health Hazard

ghs07

Harmful

信号词 Danger
危险声明 H373: Causes damage to organs through prolonged or repeated exposure
H413: May cause long lasting harmful effects to aquatic life
H302: Harmful if swallowed
H350: May cause cancer
H361: Suspected of damaging fertility or the unborn child
预防措施声明 P273,P280,P405,P501,P264,P260,P270,P330,P203,P301+P317,P318,P319

靶标

Target ID 1943
名称 B-Raf proto-oncogene, serine/threonine kinase
缩写名 B-Raf
家族 RAF family
基因和蛋白信息
Species Transmembrane Domains Amino Acids Chromosomal Location Gene Symbol Gene Name
Human 2 766 7q34 BRAF B-Raf proto-oncogene, serine/threonine kinase
Mouse 2 804 6 18.43 cM Braf Braf transforming gene
Rat 2 804 4q21-q22 Braf B-Raf proto-oncogene, serine/threonine kinase
Ensembl Gene ENSG00000157764 (Hs) , ENSMUSG00000002413 (Mm) , ENSRNOG00000010957 (Rn)
Entrez Gene 673 (Hs) , 109880 (Mm) , 114486 (Rn)
OMIM 164757 (Hs)
UniProtKB P15056 (Hs) , P28028 (Mm)
RefSeq Nucleotide NM_004333 (Hs) , NM_139294 (Mm) , XM_231692 (Rn)
RefSeq Protein NP_004324 (Hs) , NP_647455 (Mm) , XP_231692 (Rn)
Orphanet 119066 (Hs)
Protein GI 33188459 (Hs) , 153791904 (Mm) , 109471941 (Rn)
UniProtKB Variant VAR_018629 (Hs)
DrugBank Target P15056 (Hs)
ChEMBL Target CHEMBL5145 (Hs) , CHEMBL2331061 (Mm)
Target ID 2184
名称 Raf-1 proto-oncogene, serine/threonine kinase
缩写名 c-Raf
家族 RAF family
基因和蛋白信息
Species Transmembrane Domains Amino Acids Chromosomal Location Gene Symbol Gene Name
Human 2 648 3p25.2 RAF1 Raf-1 proto-oncogene, serine/threonine kinase
Mouse 2 648 6 53.62 cM Raf1 v-raf-leukemia viral oncogene 1
Rat 2 648 4q42 Raf1 Raf-1 proto-oncogene, serine/threonine kinase
Ensembl Gene ENSG00000132155 (Hs) , ENSMUSG00000000441 (Mm) , ENSRNOG00000010153 (Rn)
Entrez Gene 5894 (Hs) , 24703 (Rn) , 110157 (Mm)
OMIM 164760 (Hs)
UniProtKB P04049 (Hs) , P11345 (Rn) , Q99N57 (Mm)
RefSeq Nucleotide NM_002880 (Hs) , NM_012639 (Rn) , NM_029780 (Mm)
RefSeq Protein NP_002871 (Hs) , NP_036771 (Rn) , NP_084056 (Mm)
Orphanet 138722 (Hs)
Protein GI 4506401 (Hs) , 18497290 (Mm) , 6981458 (Rn)
DrugBank Target P04049 (Hs)
ChEMBL Target CHEMBL1906 (Hs) , CHEMBL3804748 (Mm)

关联配体

Ligand ID 5893
名称 vemurafenib
别名 PLX4032
类别 Synthetic organic
学名 N-(3-{[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]carbonyl}-2,4-difluorophenyl)propane-1-sulfonamide
生物活性评价 The sulfonamide class of antibacterial compounds are primarily bacteriostatic agents and have a broad spectrum of activity against both Gram-positive and Gram-negative species of bacteria (reviewed in ).
评价 Vemurafenib is a Type-2 kinase inhibitor and was first approved by the FDA in 2011.

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