ID: ALA2333727

Max Phase: Preclinical

Molecular Formula: C18H32O7

Molecular Weight: 360.45

Molecule Type: Small molecule

Representations

Canonical SMILES:  CCCCCCCCOCC#CCOC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O

Standard InChI:  InChI=1S/C18H32O7/c1-2-3-4-5-6-7-10-23-11-8-9-12-24-13-14-15(19)16(20)17(21)18(22)25-14/h14-22H,2-7,10-13H2,1H3/t14-,15+,16+,17-,18+/m1/s1

Standard InChI Key:  ZVRLQNBKIBNORM-ICUGJSFKSA-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: 360.45

Molecular Weight (Monoisotopic): 360.2148

AlogP: 0.18

#Rotatable Bonds: 11

Polar Surface Area: 108.61

Molecular Species: NEUTRAL

HBA: 7

HBD: 4

#RO5 Violations: 0

HBA (Lipinski): 7

HBD (Lipinski): 4

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 11.30

CX Basic pKa:

CX LogP: 1.24

CX LogD: 1.24

Aromatic Rings: 0

Heavy Atoms: 25

QED Weighted: 0.31

Np Likeness Score: 1.17

References

1. Chaveriat L, Gosselin I, Machut C, Martin P..  (2013)  Synthesis, surface tension properties and antibacterial activities of amphiphilic D-galactopyranose derivatives.,  62  [PMID:23353739] [10.1016/j.ejmech.2012.12.032]

Source

Source(1):

• Scientific Literature