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Chemical structure of Orantinib

GC62291

Orantinib

Also listed as (Z)-Orantinib

(Z)-Orantinib ((Z)-SU6668) is a potent, selective, orally active and ATP competitive inhibitor of Flk‐1/KDR, PDGFRβ, and FGFR1, with IC50s of 2·1, 0·008, and 1·2 ?M, respectively· (Z)-Orantinib is a potent antiangiogenic and antitumor agent that induces regression of established tumors

ChemicalCAS210644-62-5MW310.35FormulaC18H18N2O3
CAS number
210644-62-5
Molecular weight
310.35
Formula
C18H18N2O3
Solubility
DMSO : 50 mg/mL (161·11 mM; Need ultrasonic)
InChIKey
NHFDRBXTEDBWCZ-ZROIWOOFSA-N
Catalogue number
GC62291
Brand
GLPBIO
Computed properties PubChem CID 5329099 · XLogP 2.2 · TPSA 82.2 Ų · H-bond donors 3
XLogP
2.2
TPSA
82.2 Ų
H-bond donors
3
H-bond acceptors
3
Rotatable bonds
4
Heavy atoms
23

SMILES CC1=C(NC(=C1CCC(=O)O)C)/C=C\2/C3=CC=CC=C3NC2=O

Computed descriptors from PubChem (CID 5329099), public domain. Identity cross-checked against the supplier's molecular formula and weight — verify before use.

Ordering in Israel

Lead time
Ships from the manufacturer to your lab in 8–14 business days; customs and cold chain handled by LABO Scientific.
Pricing
Quoted in ILS, excl. VAT. Add the item to your quote and we confirm the final price, usually the same business day.
Documents
Lot certificate of analysis and manufacturer SDS are emailed with your order confirmation.
Who we serve
Universities, hospitals and biotech companies across Israel. Research use only — not for diagnostic or therapeutic use.