DIHYDROAJUGAMARIN

ID: ALA2269697

Max Phase: Preclinical

Molecular Formula: C29H42O10

Molecular Weight: 550.65

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCC(C)C(=O)O[C@@H]1CC[C@]2(CO2)[C@]2(COC(C)=O)[C@@H](OC(C)=O)C[C@@H](C)[C@](C)(C[C@H](O)C3=CC(=O)OC3)[C@@H]12

Standard InChI:  InChI=1S/C29H42O10/c1-7-16(2)26(34)39-22-8-9-28(14-37-28)29(15-36-18(4)30)23(38-19(5)31)10-17(3)27(6,25(22)29)12-21(32)20-11-24(33)35-13-20/h11,16-17,21-23,25,32H,7-10,12-15H2,1-6H3/t16?,17-,21+,22-,23+,25-,27+,28+,29-/m1/s1

Standard InChI Key:  BRIXIZXUQQCUIP-DSFBDFPZSA-N

Associated Targets(non-human)

Athalia rosae ruficornis 105 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: 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: 550.65Molecular Weight (Monoisotopic): 550.2778AlogP: 2.88#Rotatable Bonds: 9
Polar Surface Area: 137.96Molecular Species: ACIDHBA: 10HBD: 1
#RO5 Violations: 1HBA (Lipinski): 10HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 5.77CX Basic pKa: CX LogP: 2.28CX LogD: 0.66
Aromatic Rings: 0Heavy Atoms: 39QED Weighted: 0.26Np Likeness Score: 3.22

References

1. Nishida R, Kawai K, Amano T, Kuwahara Y.  (2004)  Pharmacophagous feeding stimulant activity of neo-clerodane diterpenoids for the turnip sawfly, Athalia rosae ruficornis,  32  (1): [10.1016/S0305-1978(03)00160-1]
2. Amano T, Nishida R, Kuwahara Y.  (1997)  Ajugatakasins A and B, New Diterpenoids fromAjuga decumbens, and Feeding Stimulative Activity of Related Neoclerodane Analogs toward the Turnip Sawfly,  61  (9): [10.1271/bbb.61.1518]

Source