ID: ALA1778155

Max Phase: Preclinical

Molecular Formula: C40H75NO14

Molecular Weight: 794.03

Molecule Type: Small molecule

Representations

Canonical SMILES:  CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](N(C)CC(C)(C)O)[C@H]2O)[C@](C)(O)C[C@@H](C)[C@H](O)[C@H](C)[C@@H](O)[C@]1(C)O

Standard InChI:  InChI=1S/C40H75NO14/c1-15-27-40(12,49)32(44)22(4)29(42)20(2)17-38(10,48)34(55-36-30(43)26(16-21(3)51-36)41(13)19-37(8,9)47)23(5)31(24(6)35(46)53-27)54-28-18-39(11,50-14)33(45)25(7)52-28/h20-34,36,42-45,47-49H,15-19H2,1-14H3/t20-,21-,22+,23+,24-,25+,26+,27-,28+,29+,30-,31+,32-,33+,34-,36+,38-,39-,40-/m1/s1

Standard InChI Key:  RFKAUOGLAMBBCJ-IIIUCYNOSA-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: 794.03

Molecular Weight (Monoisotopic): 793.5188

AlogP: 1.72

#Rotatable Bonds: 9

Polar Surface Area: 217.30

Molecular Species: BASE

HBA: 15

HBD: 7

#RO5 Violations: 3

HBA (Lipinski): 15

HBD (Lipinski): 7

#RO5 Violations (Lipinski): 3

CX Acidic pKa: 12.45

CX Basic pKa: 9.50

CX LogP: 1.93

CX LogD: -0.17

Aromatic Rings: 0

Heavy Atoms: 55

QED Weighted: 0.17

Np Likeness Score: 1.62

References

1. Liu Y, Carreras CW, Claypool M, Myles DC, Shaw SJ..  (2011)  The role of the 4''-hydroxyl on motilin agonist potency in the 9-dihydroerythromycin series.,  21  (12): [PMID:21570844] [10.1016/j.bmcl.2011.04.078]

Source

Source(1):

• Scientific Literature