ID: ALA3781292

Max Phase: Preclinical

Molecular Formula: C35H26F4N6O6

Molecular Weight: 702.62

Molecule Type: Small molecule

Representations

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

Standard InChI:  InChI=1S/C35H26F4N6O6/c1-48-25-14-31(47)35(34(15-25)49-2)30(46)9-3-20-4-10-32(50-18-23-16-44(42-40-23)28-7-5-21(36)12-26(28)38)33(11-20)51-19-24-17-45(43-41-24)29-8-6-22(37)13-27(29)39/h3-17,47H,18-19H2,1-2H3/b9-3+

Standard InChI Key:  LOKKWZASVFDPKI-YCRREMRBSA-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: 702.62

Molecular Weight (Monoisotopic): 702.1850

AlogP: 6.18

#Rotatable Bonds: 13

Polar Surface Area: 135.64

Molecular Species: NEUTRAL

HBA: 12

HBD: 1

#RO5 Violations: 3

HBA (Lipinski): 12

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 3

CX Acidic pKa: 7.19

CX Basic pKa:

CX LogP: 7.20

CX LogD: 6.79

Aromatic Rings: 6

Heavy Atoms: 51

QED Weighted: 0.08

Np Likeness Score: -0.55

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