ID: ALA4521972

Max Phase: Preclinical

Molecular Formula: C38H40N6O11

Molecular Weight: 756.77

Molecule Type: Unknown

Representations

Canonical SMILES:  NC[C@H]1O[C@@H](O[C@@H](Cc2cn(Cc3ccc(COc4ccc(C(=O)c5ccccc5)cc4)cc3)nn2)[C@H]2O[C@@H](n3ccc(=O)[nH]c3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H]1O

Standard InChI:  InChI=1S/C38H40N6O11/c39-17-28-31(47)34(50)37(54-28)53-27(35-32(48)33(49)36(55-35)44-15-14-29(45)40-38(44)51)16-25-19-43(42-41-25)18-21-6-8-22(9-7-21)20-52-26-12-10-24(11-13-26)30(46)23-4-2-1-3-5-23/h1-15,19,27-28,31-37,47-50H,16-18,20,39H2,(H,40,45,51)/t27-,28+,31+,32-,33+,34+,35+,36+,37+/m0/s1

Standard InChI Key:  BFQARAORPOXDHX-BQKAZMJOSA-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: 756.77

Molecular Weight (Monoisotopic): 756.2755

AlogP: -0.36

#Rotatable Bonds: 14

Polar Surface Area: 246.50

Molecular Species: BASE

HBA: 16

HBD: 6

#RO5 Violations: 3

HBA (Lipinski): 17

HBD (Lipinski): 7

#RO5 Violations (Lipinski): 3

CX Acidic pKa: 9.70

CX Basic pKa: 8.75

CX LogP: 0.95

CX LogD: -0.17

Aromatic Rings: 5

Heavy Atoms: 55

QED Weighted: 0.08

Np Likeness Score: 0.11

References

1. Patel B, Ryan P, Makwana V, Zunk M, Rudrawar S, Grant G..  (2019)  Caprazamycins: Promising lead structures acting on a novel antibacterial target MraY.,  171  [PMID:30933853] [10.1016/j.ejmech.2019.01.071]

2. Serpi M, Ferrari V, Pertusati F..  (2016)  Nucleoside Derived Antibiotics to Fight Microbial Drug Resistance: New Utilities for an Established Class of Drugs?,  59  (23): [PMID:27607900] [10.1021/acs.jmedchem.6b00325]

Source

Source(1):

• Scientific Literature