ID: ALA5186229

Max Phase: Preclinical

Molecular Formula: C29H27ClFN5O3

Molecular Weight: 548.02

Associated Items:

Representations

Canonical SMILES:  Cn1nc2c(=O)n(CC3(O)CCN(Cc4ccc(-c5ccco5)cc4Cl)CC3)cnc2c1-c1ccc(F)cc1

Standard InChI:  InChI=1S/C29H27ClFN5O3/c1-34-27(19-6-8-22(31)9-7-19)25-26(33-34)28(37)36(18-32-25)17-29(38)10-12-35(13-11-29)16-21-5-4-20(15-23(21)30)24-3-2-14-39-24/h2-9,14-15,18,38H,10-13,16-17H2,1H3

Standard InChI Key:  QRSMRDQGARXWNY-UHFFFAOYSA-N

Associated Targets(Human)

Ubiquitin carboxyl-terminal hydrolase 7 837 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ubiquitin carboxyl-terminal hydrolase 2 8818 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Probable ubiquitin carboxyl-terminal hydrolase FAF-X 500 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ubiquitin carboxyl-terminal hydrolase 11 16 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ubiquitin carboxyl-terminal hydrolase 25 268 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ubiquitin carboxyl-terminal hydrolase 28 268 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ubiquitin carboxyl-terminal hydrolase 47 99 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ubiquitin carboxyl-terminal hydrolase isozyme L1 107 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ubiquitin carboxyl-terminal hydrolase isozyme L5 42 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Splenocyte 1641 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MC-38 857 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: 548.02Molecular Weight (Monoisotopic): 547.1786AlogP: 4.88#Rotatable Bonds: 6
Polar Surface Area: 89.32Molecular Species: NEUTRALHBA: 8HBD: 1
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 7.77CX LogP: 3.77CX LogD: 3.24
Aromatic Rings: 5Heavy Atoms: 39QED Weighted: 0.33Np Likeness Score: -1.27

References

1. Li X, Yang S, Zhang H, Liu X, Gao Y, Chen Y, Liu L, Wang D, Liang Z, Liu S, Dai L, Xu Q, Yuan H, Chen C, Sun H, Wen X..  (2022)  Discovery of Orally Bioavailable N-Benzylpiperidinol Derivatives as Potent and Selective USP7 Inhibitors with In Vivo Antitumor Immunity Activity against Colon Cancer.,  65  (24.0): [PMID:36454192] [10.1021/acs.jmedchem.2c01444]

Source