Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4745618
Max Phase: Preclinical
Molecular Formula: C28H35N5O7
Molecular Weight: 553.62
Molecule Type: Unknown
Associated Items:
ID: ALA4745618
Max Phase: Preclinical
Molecular Formula: C28H35N5O7
Molecular Weight: 553.62
Molecule Type: Unknown
Associated Items:
Canonical SMILES: N[C@H]1CCC(=O)NCC[C@@H](C(=O)NCc2ccccc2CC(=O)O)NC(=O)C[C@H](Cc2ccc(O)cc2)NC1=O
Standard InChI: InChI=1S/C28H35N5O7/c29-22-9-10-24(35)30-12-11-23(28(40)31-16-19-4-2-1-3-18(19)14-26(37)38)33-25(36)15-20(32-27(22)39)13-17-5-7-21(34)8-6-17/h1-8,20,22-23,34H,9-16,29H2,(H,30,35)(H,31,40)(H,32,39)(H,33,36)(H,37,38)/t20-,22-,23-/m0/s1
Standard InChI Key: YPOQRJZHCULELI-PMVMPFDFSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
Molecule Type: Unknown | Topical: No | First In Class: No | Black Box: No |
Chirality: No | Availability: No | Prodrug: No |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 553.62 | Molecular Weight (Monoisotopic): 553.2536 | AlogP: -0.13 | #Rotatable Bonds: 7 |
Polar Surface Area: 199.95 | Molecular Species: ACID | HBA: 7 | HBD: 7 |
#RO5 Violations: 2 | HBA (Lipinski): 12 | HBD (Lipinski): 8 | #RO5 Violations (Lipinski): 3 |
CX Acidic pKa: 4.22 | CX Basic pKa: 8.20 | CX LogP: -3.10 | CX LogD: -3.16 |
Aromatic Rings: 2 | Heavy Atoms: 40 | QED Weighted: 0.25 | Np Likeness Score: 0.34 |
1. Barlow, Nicholas, Vanga, Sudarsana Reddy, Savmarker, Jonas, Sandstrom, Anja, Burns, Peta, Hallberg, Anders, Aqvist, Johan, Gutierrez-de-Teran, Hugo, Hallberg, Mathias, Larhed, Mats, Chai, Siew Yeen, Thompson, Philip E.. (2020) Macrocyclic peptidomimetics as inhibitors of insulin-regulated aminopeptidase (IRAP), 11 (2): [PMID:33479630] [10.1039/c9md00485h] |
Source(1):