ID: ALA5285952

Max Phase: Preclinical

Molecular Formula: C23H28FN3O4

Molecular Weight: 429.49

Representations

Canonical SMILES:  C[C@@H]1[C@@H](n2cc(-c3ccc(F)cc3)nn2)O[C@@H]2O[C@@]3(C)CC[C@H]4[C@H](C)CC[C@@H]1[C@@]24OO3

Standard InChI:  InChI=1S/C23H28FN3O4/c1-13-4-9-18-14(2)20(27-12-19(25-26-27)15-5-7-16(24)8-6-15)28-21-23(18)17(13)10-11-22(3,29-21)30-31-23/h5-8,12-14,17-18,20-21H,4,9-11H2,1-3H3/t13-,14+,17+,18+,20+,21-,22-,23-/m1/s1

Standard InChI Key:  PIVSJHSNHHNFEF-GEICPYOASA-N

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

Properties

Molecular Weight: 429.49

Molecular Weight (Monoisotopic): 429.2064

AlogP: 4.46

#Rotatable Bonds: 2

Polar Surface Area: 67.63

Molecular Species: NEUTRAL

HBA: 7

HBD: 0

#RO5 Violations: 0

HBA (Lipinski): 7

HBD (Lipinski): 0

#RO5 Violations (Lipinski): 0

CX Acidic pKa:

CX Basic pKa:

CX LogP: 5.55

CX LogD: 5.55

Aromatic Rings: 2

Heavy Atoms: 31

QED Weighted: 0.66

Np Likeness Score: 1.27

References

1. Gao F, Sun Z, Kong F, Xiao J..  (2020)  Artemisinin-derived hybrids and their anticancer activity.,  188  [PMID:31945642] [10.1016/j.ejmech.2020.112044]

Source

Source(1):

• Scientific Literature