ID: ALA4643686

Max Phase: Preclinical

Molecular Formula: C22H28N6O4

Molecular Weight: 440.50

Molecule Type: Unknown

Representations

Canonical SMILES:  O=C(C[C@@H](CC1CCCC1)C(=O)N1CC2(CC2)C[C@H]1c1nc(-c2cnccn2)no1)NO

Standard InChI:  InChI=1S/C22H28N6O4/c29-18(26-31)10-15(9-14-3-1-2-4-14)21(30)28-13-22(5-6-22)11-17(28)20-25-19(27-32-20)16-12-23-7-8-24-16/h7-8,12,14-15,17,31H,1-6,9-11,13H2,(H,26,29)/t15-,17+/m1/s1

Standard InChI Key:  LTYSLAIMYZKRMR-WBVHZDCISA-N

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Unknown

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Properties

Molecular Weight: 440.50

Molecular Weight (Monoisotopic): 440.2172

AlogP: 2.67

#Rotatable Bonds: 7

Polar Surface Area: 134.34

Molecular Species: NEUTRAL

HBA: 8

HBD: 2

#RO5 Violations: 0

HBA (Lipinski): 10

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 8.90

CX Basic pKa: 0.70

CX LogP: 1.31

CX LogD: 1.29

Aromatic Rings: 2

Heavy Atoms: 32

QED Weighted: 0.50

Np Likeness Score: -0.57

References

1. Hu L, Cai X, Dong S, Zhen Y, Hu J, Wang S, Jiang J, Huang J, Han Y, Qian Y, Yuan Y, Hu W..  (2020)  Synthesis and Anticancer Activity of Novel Actinonin Derivatives as HsPDF Inhibitors.,  63  (13): [PMID:32551649] [10.1021/acs.jmedchem.0c00079]

Source

Source(1):

• Scientific Literature