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Chemical structure of ST271

GC30180

ST271

Also known as (E)-2-cyano-3-[4-hydroxy-3,5-di(propan-2-yl)phenyl]prop-2-enamide

ST271 is a potent inhibitor of protein tyrosine kinase (PTK), inhibits phospholipase D activation stimulated by fMet-Leu-Phe and PAF, with IC50s of 6·7 and 9 μM, respectively

ChemicalCAS106392-48-7MW272.34FormulaC16H20N2O2
CAS number
106392-48-7
Molecular weight
272.34
Formula
C16H20N2O2
Solubility
DMSO ： ≥ 110 mg/mL (403·91 mM)
InChIKey
HMLQHJRJKQDTKW-LFYBBSHMSA-N
Catalogue number
GC30180
Brand
GLPBIO
Computed properties PubChem CID 6439072 · XLogP 3 · TPSA 87.1 Ų · H-bond donors 2
XLogP
3
TPSA
87.1 Ų
H-bond donors
2
H-bond acceptors
3
Rotatable bonds
4
Heavy atoms
20

SMILES CC(C)C1=CC(=CC(=C1O)C(C)C)/C=C(\C#N)/C(=O)N

Computed descriptors from PubChem (CID 6439072), 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
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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.