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TIE-2/VEGFR-2 kinase-IN-1 Size:Contact [email protected] for quotation Oleoylethanolamide suppresses TGF-β1 induced hepatic

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Description

Oleoylethanolamide suppresses TGF-β1 induced hepatic stellate cells (HSCs) activation in vitro via PPAR-α

39-tridecaazadotetracontanamido)-6

ABT-702 potently inhibits the activity of rat brain cytosolic AK in a concentration-dependent manner with an IC50 value of 1

The potent localized inhibition of sebaceous glands by RU 58841 demonstrates the excellent potential of this compound as a topical drug for the treatment of acne and other androgen-mediated disorders

InChi: InChI=1S/C10H7NO3/c12-8-4-3-7(10(13)14)6-2-1-5-11-9(6)8/h1-5

TIE-2/VEGFR-2 kinase-IN-1 Size:Contact [email protected] for quotation Oleoylethanolamide suppresses TGF-β1 induced hepaticTIE 2 VEGFR 2 kinase IN 1 is used for the synthesis of TIE 2 and or VEGFR 2 inhibitors, extracted from patent WO2003022852, example 14. TIE 2 VEGFR 2 kinase IN 1 is used for the study of diseases associated with inappropriate angiogenesis. Product information CAS Number: 453590 24 4 Molecular Weight: 241. 25 Formula: C13H11N3O2 Chemical Name: 6 (4 methoxyphenyl)furo[2,3 d]pyrimidin 4 amine Smiles: COC1=CC=C(C=C1)C1=CC2=C(N=CN=C2N)O1 InChiKey:

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