4,12-SECO-4,12-DIOXORYANODIN

ID: ALA2273072

Max Phase: Preclinical

Molecular Formula: C25H33NO9

Molecular Weight: 491.54

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)[C@@]1(O)[C@@H](OC(=O)c2ccc[nH]2)C(=O)[C@@]2(C)C[C@]3(O)O[C@]4(C(=O)[C@]13C)[C@H](O)[C@@H](C)CC[C@@]42O

Standard InChI:  InChI=1S/C25H33NO9/c1-12(2)24(33)17(34-18(29)14-7-6-10-26-14)16(28)20(4)11-23(32)21(24,5)19(30)25(35-23)15(27)13(3)8-9-22(20,25)31/h6-7,10,12-13,15,17,26-27,31-33H,8-9,11H2,1-5H3/t13-,15+,17-,20+,21-,22-,23-,24+,25-/m0/s1

Standard InChI Key:  ZAWQSHZZSAUOKQ-DSYIDWKTSA-N

Associated Targets(non-human)

Musca domestica 713 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ryanodine receptor 1 126 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: 491.54Molecular Weight (Monoisotopic): 491.2155AlogP: 0.47#Rotatable Bonds: 3
Polar Surface Area: 166.38Molecular Species: NEUTRALHBA: 9HBD: 5
#RO5 Violations: 0HBA (Lipinski): 10HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.29CX Basic pKa: CX LogP: 2.11CX LogD: 2.11
Aromatic Rings: 1Heavy Atoms: 35QED Weighted: 0.38Np Likeness Score: 1.63

References

1. Jefferies PR, Lehmberg E, Lam WW, Casida JE..  (1993)  Bioactive ryanoids from nucleophilic additions to 4,12-seco-4,12-dioxoryanodine.,  36  (9): [PMID:8387597] [10.1021/jm00061a003]

Source