ID: ALA4590913

Max Phase: Preclinical

Molecular Formula: C24H31NO5

Molecular Weight: 413.51

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C/C1=C\CC[C@@]2(C)O[C@@H]2[C@H]2OC(=O)[C@@H](CN[C@@H](Cc3ccccc3)C(=O)O)[C@@H]2CC1

Standard InChI:  InChI=1S/C24H31NO5/c1-15-7-6-12-24(2)21(30-24)20-17(11-10-15)18(23(28)29-20)14-25-19(22(26)27)13-16-8-4-3-5-9-16/h3-5,7-9,17-21,25H,6,10-14H2,1-2H3,(H,26,27)/b15-7+/t17-,18-,19-,20-,21+,24+/m0/s1

Standard InChI Key:  QJNBFVWGYRMELV-XSRRXYDUSA-N

Associated Targets(Human)

MEC1 72 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 413.51Molecular Weight (Monoisotopic): 413.2202AlogP: 3.11#Rotatable Bonds: 6
Polar Surface Area: 88.16Molecular Species: ZWITTERIONHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 1.51CX Basic pKa: 10.12CX LogP: 1.21CX LogD: 1.21
Aromatic Rings: 1Heavy Atoms: 30QED Weighted: 0.42Np Likeness Score: 2.11

References

1. Li X, Payne DT, Ampolu B, Bland N, Brown JT, Dutton MJ, Fitton CA, Gulliver A, Hale L, Hamza D, Jones G, Lane R, Leach AG, Male L, Merisor EG, Morton MJ, Quy AS, Roberts R, Scarll R, Schulz-Utermoehl T, Stankovic T, Stevenson B, Fossey JS, Agathanggelou A..  (2019)  Derivatisation of parthenolide to address chemoresistant chronic lymphocytic leukaemia.,  10  (8): [PMID:32952998] [10.1039/C9MD00297A]

Source