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ID: ALA4474790
Max Phase: Preclinical
Molecular Formula: C70H109N17O12
Molecular Weight: 1380.75
Molecule Type: Unknown
Associated Items:
ID: ALA4474790
Max Phase: Preclinical
Molecular Formula: C70H109N17O12
Molecular Weight: 1380.75
Molecule Type: Unknown
Associated Items:
Canonical SMILES: CCCC[C@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CCCNC(=N)N)N(C)C(=O)[C@H](N)CCCCN)C(C)C)C(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](CCCCN)C(=O)O
Standard InChI: InChI=1S/C70H109N17O12/c1-7-8-25-51(61(90)83-56(40-46-41-78-50-26-13-12-23-48(46)50)63(92)79-52(27-15-18-35-72)60(89)81-53(69(98)99)28-16-19-36-73)80-66(95)58(42(2)3)86-67(96)59(43(4)5)85-64(93)55(39-45-30-32-47(88)33-31-45)82-62(91)54(38-44-21-10-9-11-22-44)84-65(94)57(29-20-37-77-70(75)76)87(6)68(97)49(74)24-14-17-34-71/h9-13,21-23,26,30-33,41-43,49,51-59,78,88H,7-8,14-20,24-25,27-29,34-40,71-74H2,1-6H3,(H,79,92)(H,80,95)(H,81,89)(H,82,91)(H,83,90)(H,84,94)(H,85,93)(H,86,96)(H,98,99)(H4,75,76,77)/t49-,51+,52+,53-,54+,55+,56+,57+,58+,59+/m1/s1
Standard InChI Key: CLTVCCLZSPKLRB-NRGGWPRRSA-N
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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: 1380.75 | Molecular Weight (Monoisotopic): 1379.8442 | AlogP: | #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: |
1. Denèfle T, Pramil E, Gómez-Morales L, Levasseur MD, Lardé E, Newton C, Herry K, Herbi L, Lamotte Y, Odile E, Ancellin N, Grondin P, Martinez-Torres AC, Viviani F, Merle-Beral H, Lequin O, Susin SA, Karoyan P.. (2019) Homotrimerization Approach in the Design of Thrombospondin-1 Mimetic Peptides with Improved Potency in Triggering Regulated Cell Death of Cancer Cells., 62 (17): [PMID:31403795] [10.1021/acs.jmedchem.9b00024] |
Source(1):