NA

ID: ALA4513307

PubChem CID: 24884921

Max Phase: Preclinical

Molecular Formula: C42H64O14

Molecular Weight: 792.96

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCCCCCC(=O)O[C@H]1/C(=C/C(=O)OC)C[C@H]2C[C@H](CO)OC(=O)C[C@H](O)C[C@@H]3CCC[C@H](C[C@@H]4C/C(=C\C(=O)OC)C[C@H](/C=C/C(C)(C)[C@]1(O)O2)O4)O3

Standard InChI:  InChI=1S/C42H64O14/c1-6-7-8-9-10-14-36(45)55-40-28(21-38(47)51-5)20-34-25-35(26-43)54-39(48)23-29(44)22-30-12-11-13-31(52-30)24-33-18-27(19-37(46)50-4)17-32(53-33)15-16-41(2,3)42(40,49)56-34/h15-16,19,21,29-35,40,43-44,49H,6-14,17-18,20,22-26H2,1-5H3/b16-15+,27-19-,28-21+/t29-,30+,31-,32+,33+,34+,35-,40+,42-/m1/s1

Standard InChI Key:  KVMNWHUUVCQHCF-YDROXOJZSA-N

Molfile:  

 
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M  END

Associated Targets(non-human)

Chikungunya virus (1339 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

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

Calculated Properties

Molecular Weight: 792.96Molecular Weight (Monoisotopic): 792.4296AlogP: 4.84#Rotatable Bonds: 10
Polar Surface Area: 193.58Molecular Species: NEUTRALHBA: 14HBD: 3
#RO5 Violations: 2HBA (Lipinski): 14HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: 10.64CX Basic pKa: CX LogP: 4.85CX LogD: 4.85
Aromatic Rings: Heavy Atoms: 56QED Weighted: 0.09Np Likeness Score: 1.64

References

1. Staveness D, Abdelnabi R, Schrier AJ, Loy BA, Verma VA, DeChristopher BA, Near KE, Neyts J, Delang L, Leyssen P, Wender PA..  (2016)  Simplified Bryostatin Analogues Protect Cells from Chikungunya Virus-Induced Cell Death.,  79  (4): [PMID:26900625] [10.1021/acs.jnatprod.5b01016]

Source