ID: ALA4528526

Max Phase: Preclinical

Molecular Formula: C40H58N2O5

Molecular Weight: 646.91

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)c1nn(-c2ccccc2)c2c1C[C@]1(C)[C@H]3C[C@@H](O)[C@@H]4[C@@H]([C@@]5(C)CCCC(C)(C)O5)CC[C@@]4(C)[C@]3(C)C[C@@H](O)[C@H]1C2(C)C

Standard InChI:  InChI=1S/C40H58N2O5/c1-10-46-34(45)31-25-22-37(6)29-21-27(43)30-26(40(9)19-14-18-35(2,3)47-40)17-20-38(30,7)39(29,8)23-28(44)32(37)36(4,5)33(25)42(41-31)24-15-12-11-13-16-24/h11-13,15-16,26-30,32,43-44H,10,14,17-23H2,1-9H3/t26-,27+,28+,29+,30-,32-,37+,38+,39+,40+/m0/s1

Standard InChI Key:  ZYWNGAURRAUGDE-JWHSEDPWSA-N

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 646.91Molecular Weight (Monoisotopic): 646.4346AlogP: 7.43#Rotatable Bonds: 4
Polar Surface Area: 93.81Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 6.86CX LogD: 6.86
Aromatic Rings: 2Heavy Atoms: 47QED Weighted: 0.34Np Likeness Score: 1.53

References

1. Wu Q, Wang R, Shi Y, Li W, Li M, Chen P, Pan B, Wang Q, Li C, Wang J, Sun G, Sun X, Fu H..  (2020)  Synthesis and biological evaluation of panaxatriol derivatives against myocardial ischemia/reperfusion injury in the rat.,  185  [PMID:31655431] [10.1016/j.ejmech.2019.111729]

Source