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Merck
CN

616400-M

Tranilast

An anthranilic acid analog that acts as a potent inhibitor of VEGF- and vascular permeability factor-induced angiogenesis and collagen synthesis.

别名:

Tranilast, N-(3ʹ,4ʹ-Dimethoxycinnamoyl)anthranilic Acid

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关于此项目

经验公式(希尔记法):
C18H17NO5
化学文摘社编号:
分子量:
327.33
UNSPSC Code:
51111800
MDL number:
NACRES:
NA.77
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SMILES string

N(c2c(cccc2)C(=O)O)C(=O)\C=C\c1cc(c(cc1)OC)OC

InChI

1S/C18H17NO5/c1-23-15-9-7-12(11-16(15)24-2)8-10-17(20)19-14-6-4-3-5-13(14)18(21)22/h3-11H,1-2H3,(H,19,20)(H,21,22)/b10-8+

InChI key

NZHGWWWHIYHZNX-CSKARUKUSA-N

description

Merck USA index - 14, 9570

assay

≥95% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, protect from light

color

pale yellow

solubility

DMSO: 200 mg/mL

storage temp.

−20°C

Quality Level

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General description

An anthranilic acid analog that acts as a potent inhibitor of VEGF- and vascular permeability factor-induced angiogenesis and collagen synthesis. Inhibits VEGF- and PMA-stimulated PKC activity in retinal capillary endothelial cells without affecting the VEGF binding or VEGF receptor phosphorylation. Also has antiallergic, anti-inflammatory, and antiproliferative properties. Induces Ca2+ mobilization in vascular smooth muscle.

Biochem/physiol Actions

Primary Target
VEGF- and vascular permeability factor-induced angiogenesis and collagen synthesis

Preparation Note

Following reconstitution, aliquot and freeze (-20°C).

Other Notes

Koyama, S., et al. 1999. Br. J. Pharmacol. 127, 537.
Isaji, M., et al. 1998. Life Sci. 63, PL71.
Isaji, M., et al. 1997. Br. J. Pharmacol. 122, 1061.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Harmful (C)

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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