ID: ALA1934273

Max Phase: Preclinical

Molecular Formula: C22H30O5

Molecular Weight: 374.48

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C=C[C@]1(C)C=C2C3(CO3)C(=O)[C@H]3C(C)(C)CCC[C@]3(C(=O)OC)[C@@]2(O)CC1

Standard InChI:  InChI=1S/C22H30O5/c1-6-19(4)10-11-22(25)14(12-19)21(13-27-21)16(23)15-18(2,3)8-7-9-20(15,22)17(24)26-5/h6,12,15,25H,1,7-11,13H2,2-5H3/t15-,19-,20-,21?,22+/m0/s1

Standard InChI Key:  GKQYRCLWWVMCRU-SAFSJCAZSA-N

Associated Targets(non-human)

Xanthomonas oryzae pv. oryzae 79 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 374.48Molecular Weight (Monoisotopic): 374.2093AlogP: 2.97#Rotatable Bonds: 2
Polar Surface Area: 76.13Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.45CX Basic pKa: CX LogP: 3.12CX LogD: 3.12
Aromatic Rings: 0Heavy Atoms: 27QED Weighted: 0.46Np Likeness Score: 3.01

References

1. Evidente A, Venturi V, Masi M, Degrassi G, Cimmino A, Maddau L, Andolfi A..  (2011)  In vitro antibacterial activity of sphaeropsidins and chemical derivatives toward Xanthomonas oryzae pv. oryzae, the causal agent of rice bacterial blight.,  74  (12): [PMID:22124378] [10.1021/np200625m]

Source