ID: ALA3781864

Max Phase: Preclinical

Molecular Formula: C27H23F2N3O6

Molecular Weight: 523.49

Molecule Type: Small molecule

Representations

Canonical SMILES:  COc1cc(O)c(C(=O)/C=C/c2ccc(OC)c(OCc3cn(-c4ccc(F)cc4F)nn3)c2)c(OC)c1

Standard InChI:  InChI=1S/C27H23F2N3O6/c1-35-19-12-23(34)27(26(13-19)37-3)22(33)8-4-16-5-9-24(36-2)25(10-16)38-15-18-14-32(31-30-18)21-7-6-17(28)11-20(21)29/h4-14,34H,15H2,1-3H3/b8-4+

Standard InChI Key:  SFJIFPSOFRFCOJ-XBXARRHUSA-N

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Properties

Molecular Weight: 523.49

Molecular Weight (Monoisotopic): 523.1555

AlogP: 4.75

#Rotatable Bonds: 10

Polar Surface Area: 104.93

Molecular Species: NEUTRAL

HBA: 9

HBD: 1

#RO5 Violations: 1

HBA (Lipinski): 9

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 1

CX Acidic pKa: 7.19

CX Basic pKa:

CX LogP: 5.40

CX LogD: 4.99

Aromatic Rings: 4

Heavy Atoms: 38

QED Weighted: 0.23

Np Likeness Score: -0.71

References

1. Kant R, Kumar D, Agarwal D, Gupta RD, Tilak R, Awasthi SK, Agarwal A..  (2016)  Synthesis of newer 1,2,3-triazole linked chalcone and flavone hybrid compounds and evaluation of their antimicrobial and cytotoxic activities.,  113  [PMID:26922227] [10.1016/j.ejmech.2016.02.041]

Source

Source(1):

• Scientific Literature