ID: ALA5191896

Max Phase: Preclinical

Molecular Formula: C39H50O8

Molecular Weight: 646.82

Associated Items:

Representations

Canonical SMILES:  COc1c(C(=O)C(C)C)c2c(c3c1[C@@H](C(C)C)C1=C(O3)C(C)(C)C(=O)C(C)(C)C1=O)[C@@H](C(C)C)C1=C(O2)C(C)(C)C(=O)C(C)(C)C1=O

Standard InChI:  InChI=1S/C39H50O8/c1-16(2)19-21-27(45-15)25(26(40)18(5)6)29-22(28(21)46-32-23(19)30(41)36(7,8)34(43)38(32,11)12)20(17(3)4)24-31(42)37(9,10)35(44)39(13,14)33(24)47-29/h16-20H,1-15H3/t19-,20-/m1/s1

Standard InChI Key:  WNADCLXGDKXCND-WOJBJXKFSA-N

Associated Targets(Human)

Tyrosyl-DNA phosphodiesterase 2 864 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Tyrosyl-DNA phosphodiesterase 1 345557 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

DU-145 51482 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

A549 127892 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: 646.82Molecular Weight (Monoisotopic): 646.3506AlogP: 7.71#Rotatable Bonds: 5
Polar Surface Area: 113.04Molecular Species: NEUTRALHBA: 8HBD: 0
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 9.01CX LogD: 9.01
Aromatic Rings: 1Heavy Atoms: 47QED Weighted: 0.24Np Likeness Score: 1.14

References

1. Zhang Y, Yang H, Wang FT, Peng X, Liu HY, Li QJ, An LK..  (2022)  Discovery, enantioselective synthesis of myrtucommulone E analogues as tyrosyl-DNA phosphodiesterase 2 inhibitors and their biological activities.,  238  [PMID:35580424] [10.1016/j.ejmech.2022.114445]

Source