NA

ID: ALA4558450

PubChem CID: 57327139

Max Phase: Preclinical

Molecular Formula: C42H66O13

Molecular Weight: 778.98

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  C=C1C[C@H]2C[C@@H]3O[C@H](C[C@@H](O)CC(=O)O[C@@H](CO)C[C@@H]4C/C(=C\C(=O)OC)[C@H](OC(=O)CCCCCCC)[C@@](O)(O4)C(C)(C)/C=C/[C@@H](C1)O2)C[C@H](O)C3(C)C

Standard InChI:  InChI=1S/C42H66O13/c1-8-9-10-11-12-13-36(46)54-39-27(19-37(47)50-7)18-32-22-33(25-43)53-38(48)21-28(44)20-31-23-34(45)41(5,6)35(52-31)24-30-17-26(2)16-29(51-30)14-15-40(3,4)42(39,49)55-32/h14-15,19,28-35,39,43-45,49H,2,8-13,16-18,20-25H2,1,3-7H3/b15-14+,27-19+/t28-,29+,30+,31-,32+,33-,34+,35+,39+,42-/m1/s1

Standard InChI Key:  PTWFFQZHJFSKIB-GYFDTONYSA-N

Molfile:  

 
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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: 778.98Molecular Weight (Monoisotopic): 778.4503AlogP: 4.91#Rotatable Bonds: 9
Polar Surface Area: 187.51Molecular Species: NEUTRALHBA: 13HBD: 4
#RO5 Violations: 2HBA (Lipinski): 13HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 10.64CX Basic pKa: CX LogP: 4.49CX LogD: 4.49
Aromatic Rings: Heavy Atoms: 55QED Weighted: 0.08Np Likeness Score: 2.06

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