ID: ALA5203237

Max Phase: Preclinical

Molecular Formula: C45H48N6O4

Molecular Weight: 736.92

Associated Items:

Representations

Canonical SMILES:  Cc1onc(-c2c3ccccc3c(Oc3ccc4ccccc4c3)c3ccccc23)c1C(=O)Nc1cc(C(=O)N(CCCN(C)C)CCCN(C)C)n(C)c1

Standard InChI:  InChI=1S/C45H48N6O4/c1-30-40(44(52)46-33-28-39(50(6)29-33)45(53)51(25-13-23-48(2)3)26-14-24-49(4)5)42(47-55-30)41-35-17-9-11-19-37(35)43(38-20-12-10-18-36(38)41)54-34-22-21-31-15-7-8-16-32(31)27-34/h7-12,15-22,27-29H,13-14,23-26H2,1-6H3,(H,46,52)

Standard InChI Key:  SWHVROPWYWNKOJ-UHFFFAOYSA-N

Associated Targets(Human)

SNB-19 46794 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: 736.92Molecular Weight (Monoisotopic): 736.3737AlogP: 8.84#Rotatable Bonds: 14
Polar Surface Area: 96.08Molecular Species: BASEHBA: 8HBD: 1
#RO5 Violations: 2HBA (Lipinski): 10HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 9.60CX LogP: 6.81CX LogD: 3.03
Aromatic Rings: 7Heavy Atoms: 55QED Weighted: 0.11Np Likeness Score: -0.81

References

1. Duncan NS, Campbell MJ, Backos DS, Li C, Rider KC, Stump S, Weaver MJ, Gajewski MP, Beall HD, Reigan P, Natale NR..  (2022)  10-Alkoxy-anthracenyl-isoxazole analogs have sub-micromolar activity against a Glioblastoma multiforme cell line.,  69  [PMID:35792402] [10.1016/j.bmc.2022.116911]

Source