(1R,2S,5R)-1-amino-2-(((R)-2-aminopropanamido)methyl)-5-(2-boronoethyl)cyclohexane-1-carboxylic acid

ID: ALA5193387

Chembl Id: CHEMBL5193387

PubChem CID: 164549394

Max Phase: Preclinical

Molecular Formula: C13H26BN3O5

Molecular Weight: 315.18

Associated Items:

Names and Identifiers

Canonical SMILES:  C[C@@H](N)C(=O)NC[C@@H]1CC[C@@H](CCB(O)O)C[C@]1(N)C(=O)O

Standard InChI:  InChI=1S/C13H26BN3O5/c1-8(15)11(18)17-7-10-3-2-9(4-5-14(21)22)6-13(10,16)12(19)20/h8-10,21-22H,2-7,15-16H2,1H3,(H,17,18)(H,19,20)/t8-,9+,10+,13-/m1/s1

Standard InChI Key:  YUZAZVPNGPARBQ-KEPMVKOISA-N

Alternative Forms

  1. Parent:

    ALA5193387

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Associated Targets(Human)

ARG1 Tchem Arginase-1 (360 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ARG2 Tchem Arginase-2, mitochondrial (9289 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

Calculated Properties

Molecular Weight: 315.18Molecular Weight (Monoisotopic): 315.1966AlogP: #Rotatable Bonds:
Polar Surface Area: Molecular Species: HBA: HBD:
#RO5 Violations: HBA (Lipinski): HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: CX LogD:
Aromatic Rings: Heavy Atoms: QED Weighted: Np Likeness Score:

References

1. Rosse G..  (2022)  Amino-cyclohexane Carboxylic Acid Inhibitors of Arginase.,  13  (10.0): [PMID:36262385] [10.1021/acsmedchemlett.2c00395]

Source