N-(3-(7-(4-Fluorophenyl)-3-hydroxy-4-oxo-4H-chromen-2-yl)phenyl)-3-methoxybenzamide

ID: ALA5186104

Chembl Id: CHEMBL5186104

PubChem CID: 168282243

Max Phase: Preclinical

Molecular Formula: C29H20FNO5

Molecular Weight: 481.48

Names and Identifiers

Canonical SMILES:  COc1cccc(C(=O)Nc2cccc(-c3oc4cc(-c5ccc(F)cc5)ccc4c(=O)c3O)c2)c1

Standard InChI:  InChI=1S/C29H20FNO5/c1-35-23-7-3-5-20(15-23)29(34)31-22-6-2-4-19(14-22)28-27(33)26(32)24-13-10-18(16-25(24)36-28)17-8-11-21(30)12-9-17/h2-16,33H,1H3,(H,31,34)

Standard InChI Key:  GCMYYTATAYIHFT-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA5186104

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Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type:

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 481.48

Molecular Weight (Monoisotopic): 481.1326

AlogP: 6.23

#Rotatable Bonds: 5

Polar Surface Area: 88.77

Molecular Species: NEUTRAL

HBA: 5

HBD: 2

#RO5 Violations: 1

HBA (Lipinski): 6

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 1

CX Acidic pKa: 9.14

CX Basic pKa: ┄

CX LogP: 5.44

CX LogD: 5.44

Aromatic Rings: 5

Heavy Atoms: 36

QED Weighted: 0.31

Np Likeness Score: -0.60

References

1. Zha D, Li Y, Luo Y, Liu Y, Lin Z, Lin C, Chen S, Wu J, Yu L, Chen S, Zhang P, Wu W, Zhang C..  (2022)  Synthesis and in vitro anticancer evaluation of novel flavonoid-based amide derivatives as regulators of the PI3K/AKT signal pathway for TNBC treatment.,  13  (9.0): [PMID:36324491] [10.1039/d2md00148a]

Source

Source(1):

• Scientific Literature