ID: ALA4879121

Max Phase: Preclinical

Molecular Formula: C29H32ClF7N6O6

Molecular Weight: 501.01

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C=CCC[C@@H]1c2cc(CNC)ccc2[C@H](NC(=O)C(=O)Nc2ccc(Cl)c(F)c2)[C@H]1CNC(=N)N.O=C(O)C(F)(F)F.O=C(O)C(F)(F)F

Standard InChI:  InChI=1S/C25H30ClFN6O2.2C2HF3O2/c1-3-4-5-16-18-10-14(12-30-2)6-8-17(18)22(19(16)13-31-25(28)29)33-24(35)23(34)32-15-7-9-20(26)21(27)11-15;2*3-2(4,5)1(6)7/h3,6-11,16,19,22,30H,1,4-5,12-13H2,2H3,(H,32,34)(H,33,35)(H4,28,29,31);2*(H,6,7)/t16-,19+,22+;;/m1../s1

Standard InChI Key:  MJIJCZZZYILOOZ-MAWPBPKCSA-N

Associated Targets(non-human)

Envelope glycoprotein gp160 755 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: 501.01Molecular Weight (Monoisotopic): 500.2103AlogP: 3.16#Rotatable Bonds: 9
Polar Surface Area: 132.13Molecular Species: BASEHBA: 4HBD: 6
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 7#RO5 Violations (Lipinski): 2
CX Acidic pKa: 10.92CX Basic pKa: 12.22CX LogP: 2.34CX LogD: -1.27
Aromatic Rings: 2Heavy Atoms: 35QED Weighted: 0.14Np Likeness Score: -0.33

References

1. Fritschi CJ, Liang S, Mohammadi M, Anang S, Moraca F, Chen J, Madani N, Sodroski JG, Abrams CF, Hendrickson WA, Smith AB..  (2021)  Identification of gp120 Residue His105 as a Novel Target for HIV-1 Neutralization by Small-Molecule CD4-Mimics.,  12  (11.0): [PMID:34795873] [10.1021/acsmedchemlett.1c00437]

Source