Amonafidazene

ID: ALA4866726

Chembl Id: CHEMBL4866726

PubChem CID: 164619670

Max Phase: Preclinical

Molecular Formula: C27H28N6O6

Molecular Weight: 532.56

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  COC(=O)N(C)/N=N/c1ccc(COC(=O)Nc2cc3c4c(cccc4c2)C(=O)N(CCN(C)C)C3=O)cc1

Standard InChI:  InChI=1S/C27H28N6O6/c1-31(2)12-13-33-24(34)21-7-5-6-18-14-20(15-22(23(18)21)25(33)35)28-26(36)39-16-17-8-10-19(11-9-17)29-30-32(3)27(37)38-4/h5-11,14-15H,12-13,16H2,1-4H3,(H,28,36)/b30-29+

Standard InChI Key:  MWXZUPHVAMRLKE-QVIHXGFCSA-N

Alternative Forms

  1. Parent:

    ALA4866726

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Associated Targets(Human)

A 172 (535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
WM 266-4 (208 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H1299 (3248 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-238 (12 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

Calculated Properties

Molecular Weight: 532.56Molecular Weight (Monoisotopic): 532.2070AlogP: 4.44#Rotatable Bonds: 8
Polar Surface Area: 133.21Molecular Species: BASEHBA: 9HBD: 1
#RO5 Violations: 1HBA (Lipinski): 12HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: 12.80CX Basic pKa: 8.52CX LogP: 4.28CX LogD: 3.14
Aromatic Rings: 3Heavy Atoms: 39QED Weighted: 0.26Np Likeness Score: -1.00

References

1. Walunj D, Thankarajan E, Prasad C, Tuchinsky H, Baldan S, Sherman MY, Patsenker L, Gellerman G..  (2021)  Targeted methylation facilitates DNA double strand breaks and enhances cancer suppression: A DNA intercalating/methylating dual-action chimera Amonafidazene.,  225  [PMID:34507011] [10.1016/j.ejmech.2021.113811]

Source