(Z)-奥兰替尼 | (Z)-SU6668 | (Z)-TSU-68
(Z)-Orantinib | (Z)-SU6668 | (Z)-TSU-68
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Product Overview
Product Name (Z)-Orantinib | (Z)-SU6668 | (Z)-TSU-68
CAS210644-62-5
FormulaC18H18N2O3
MW310.35
AppearanceOrange to red powder
Storage conditionStore in a dry and dark sealed container, short-term (weeks to months) storage at 0-4 ℃, long-term (months to years) storage at -20 ℃.
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Product details

(Z)-Orantinib ((Z)-SU6668) is a potent, selective, orally active and ATP competitive inhibitor of Flk‐1/KDR, PDGFRβ, and FGFR1, with IC 50 s of 2.1, 0.008, and 1.2 μM, respectively. (Z)-Orantinib is a potent antiangiogenic and antitumor agent that induces established tumor regression.


Related
Orantinib | SU 6668 | TSU-68
History
Retigabine (Synonyms: D-23129;N-(2-amino-4-[fluorobenzylamino]-phenyl) carbamic acid )
Ozagrel
Rebastinib (DCC-2036)
Tesirine | SG3249
(Z)-Orantinib | (Z)-SU6668 | (Z)-TSU-68
Ristomycin Monosulfate | Ristocetin Sulfate salt | Ristomycin Sulfate
4-Amino-1-benzylpiperidine-4-carboxylic acid
SGX-523
Apatinib | Apatinib Free base | YN968D1| Rivoceranib
Coelenteramine 400a (Synonyms:Coelenterazine 400a; Bisdeoxycoelenterazine)