ID: ALA2316674

Max Phase: Preclinical

Molecular Formula: C38H56N4O11

Molecular Weight: 744.88

Molecule Type: Small molecule

Representations

Canonical SMILES:  CC[C@H]1OC(=O)[C@H](C)C(=O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](N(C)C)[C@H]2O)[C@](C)(OC)C[C@@H](C)/C(=N\OCC#Cc2cncnc2)[C@H](C)[C@H]2OC(=O)O[C@@]21C

Standard InChI:  InChI=1S/C38H56N4O11/c1-12-28-38(8)33(52-36(46)53-38)23(4)29(41-48-15-13-14-26-18-39-20-40-19-26)21(2)17-37(7,47-11)32(24(5)30(43)25(6)34(45)50-28)51-35-31(44)27(42(9)10)16-22(3)49-35/h18-25,27-28,31-33,35,44H,12,15-17H2,1-11H3/b41-29+/t21-,22-,23+,24+,25-,27+,28-,31-,32-,33-,35+,37-,38-/m1/s1

Standard InChI Key:  MVADRHURRVRRCU-QKIZNIJLSA-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: 744.88

Molecular Weight (Monoisotopic): 744.3946

AlogP: 3.55

#Rotatable Bonds: 7

Polar Surface Area: 177.43

Molecular Species: NEUTRAL

HBA: 15

HBD: 1

#RO5 Violations: 2

HBA (Lipinski): 15

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 2

CX Acidic pKa: 8.93

CX Basic pKa: 8.27

CX LogP: 4.81

CX LogD: 4.20

Aromatic Rings: 1

Heavy Atoms: 53

QED Weighted: 0.14

Np Likeness Score: 1.04

References

1. Liang JH, An K, Lv W, Cushman M, Wang H, Xu YC..  (2013)  Synthesis, antibacterial activity and docking of 14-membered 9-O-(3-arylalkyl) oxime 11,12-cyclic carbonate ketolides.,  59  [PMID:23202851] [10.1016/j.ejmech.2012.10.054]

Source

Source(1):

• Scientific Literature