Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4761376
Max Phase: Preclinical
Molecular Formula: C27H33N5O7
Molecular Weight: 539.59
Molecule Type: Unknown
Associated Items:
ID: ALA4761376
Max Phase: Preclinical
Molecular Formula: C27H33N5O7
Molecular Weight: 539.59
Molecule Type: Unknown
Associated Items:
Canonical SMILES: N[C@H]1CNC(=O)CC[C@@H](C(=O)NCc2ccccc2CC(=O)O)NC(=O)C[C@H](Cc2ccc(O)cc2)NC1=O
Standard InChI: InChI=1S/C27H33N5O7/c28-21-15-29-23(34)10-9-22(27(39)30-14-18-4-2-1-3-17(18)12-25(36)37)32-24(35)13-19(31-26(21)38)11-16-5-7-20(33)8-6-16/h1-8,19,21-22,33H,9-15,28H2,(H,29,34)(H,30,39)(H,31,38)(H,32,35)(H,36,37)/t19-,21-,22-/m0/s1
Standard InChI Key: LHEAVDTVJWSJOW-BVSLBCMMSA-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: 539.59 | Molecular Weight (Monoisotopic): 539.2380 | AlogP: -0.52 | #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: 7.41 | CX LogP: -3.16 | CX LogD: -3.41 |
Aromatic Rings: 2 | Heavy Atoms: 39 | QED Weighted: 0.24 | Np Likeness Score: 0.28 |
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):