ID: ALA1778049

Max Phase: Preclinical

Molecular Formula: C39H73NO13

Molecular Weight: 764.01

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[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](N(C)C[C@H](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/C39H73NO13/c1-14-28-39(11,47)33(44)24(6)30(42)20(2)16-38(10,46)34(53-36-31(43)27(15-22(4)50-36)40(12)19-21(3)41)25(7)32(26(8)35(45)51-28)52-29-18-37(9,48-13)17-23(5)49-29/h20-34,36,41-44,46-47H,14-19H2,1-13H3/t20-,21+,22-,23+,24+,25+,26-,27+,28-,29+,30+,31-,32+,33-,34-,36+,37+,38-,39-/m1/s1

Standard InChI Key:  FQVHPYBTRDZBGK-AHJOAPQOSA-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: 764.01

Molecular Weight (Monoisotopic): 763.5082

AlogP: 2.36

#Rotatable Bonds: 9

Polar Surface Area: 197.07

Molecular Species: BASE

HBA: 14

HBD: 6

#RO5 Violations: 3

HBA (Lipinski): 14

HBD (Lipinski): 6

#RO5 Violations (Lipinski): 3

CX Acidic pKa: 12.58

CX Basic pKa: 9.20

CX LogP: 2.34

CX LogD: 0.53

Aromatic Rings: 0

Heavy Atoms: 53

QED Weighted: 0.19

Np Likeness Score: 1.52

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