ID: ALA5286523

Max Phase: Preclinical

Molecular Formula: C20H20O6

Molecular Weight: 356.37

Associated Items:

Representations

Canonical SMILES:  CC1=C2C(=CC[C@]3(CO3)[C@@H]3[C@@H]2[C@]2(C)O[C@@H]2[C@@]24C[C@@H](C)C(=O)[C@@]32O4)OC1=O

Standard InChI:  InChI=1S/C20H20O6/c1-8-6-19-16-17(3,25-16)12-11-9(2)15(22)24-10(11)4-5-18(7-23-18)13(12)20(19,26-19)14(8)21/h4,8,12-13,16H,5-7H2,1-3H3/t8-,12-,13+,16+,17+,18+,19+,20+/m1/s1

Standard InChI Key:  STCVPWDGXBXQQN-ZQJKXGJFSA-N

Associated Targets(Human)

HeLa 62764 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HEp-2 3859 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Respiratory syncytial virus 3434 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bacillus subtilis 32866 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Plasmodium falciparum 966862 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 356.37Molecular Weight (Monoisotopic): 356.1260AlogP: 1.44#Rotatable Bonds: 0
Polar Surface Area: 80.96Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 1.14CX LogD: 1.14
Aromatic Rings: 0Heavy Atoms: 26QED Weighted: 0.48Np Likeness Score: 2.26

References

1. Mahambo ET, Uwamariya C, Miah M, Clementino LDC, Alvarez LCS, Di Santo Meztler GP, Trybala E, Said J, Wieske LHE, Ward JS, Rissanen K, Munissi JJE, Costa FTM, Sunnerhagen P, Bergström T, Nyandoro SS, Erdelyi M..  (2023)  Crotofolane Diterpenoids and Other Constituents Isolated from Croton kilwae.,  86  (2.0): [PMID:36749598] [10.1021/acs.jnatprod.2c01007]

Source