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SML3750

SR-302

≥98% (HPLC)

别名:

N-(4-(((S)-4-Cyclohexyl-1-(((SR)-1-(methylsulfonyl)piperidin-3-yl)amino)-1-oxobutan-2-yl)carbamoyl)benzyl)imidazo[1,2-a]-pyridine-3-carboxamide, N-(4-((2S)-4-Cyclohexyl-1-(1-(methylsulfonyl)piperidin-3-ylamino)-1-oxobutan-2-ylcarbamoyl)benzyl)imidazo[1,2-a]pyridine-3-carboxamide, SR 302, SR302

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关于此项目

经验公式（希尔记法）:
C32H42N6O5S
化学文摘社编号:
2771319-74-3
分子量:
622.78
UNSPSC Code:
12352200
NACRES:
NA.21
Assay:
≥98% (HPLC)
Form:
powder
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Quality Segment

100

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

-10 to -25°C

SMILES string

O=C(NCC1=CC=C(C=C1)C(N[C@H](C(NC2CN(CCC2)S(=O)(C)=O)=O)CCC3CCCCC3)=O)C4=CN=C5C=CC=CN54

InChI

1S/C32H42N6O5S/c1-44(42,43)37-18-7-10-26(22-37)35-31(40)27(17-14-23-8-3-2-4-9-23)36-30(39)25-15-12-24(13-16-25)20-34-32(41)28-21-33-29-11-5-6-19-38(28)29/h5-6,11-13,15-16,19,21,23,26-27H,2-4,7-10,14,17-18,20,22H2,1H3,(H,34,41)(H,35,40)(H,36,39)/t26?,27-/m

InChI key

WGMNFJAFXXXRLZ-GEVKEYJPSA-N

Biochem/physiol Actions

Potent ATP-competitive inhibitor against DDR1, DDR2; MAPK11 (p38β), and MAPK14 (p38α) with good cellular target actviity and kinome selectivity.
SR-302 is an ATP-competitive, potent and selective inhibitor against DDR1/2 & MAPK11/14 (IC50/[ATP] = 53.3 nM/100 μM/DDR1, 0.75 nM/5 μM/DDR2; 45.1 nM/50 μM/MAPK11 (p38β), 6.2 nM/2.5 μM/MAPK14 (p38α) by cell-free kinase assay) with good cellular target actviity (IC50 = 18 nM/DDR2, 23 nM/DDR1, 125 nM/MAPK14, 196 nM/MAPK11 by NanoBRET) and kinome selectivity.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000503255
0000503257
0000503257
0000503255
0000277507

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全球贸易项目编号

货号GTIN
SML3750-1MG04065270447364
SML3750-5MG04065270447371