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ID: ALA2303853
Max Phase: Preclinical
Molecular Formula: C16H27NO12
Molecular Weight: 425.39
Molecule Type: Small molecule
Associated Items:
ID: ALA2303853
Max Phase: Preclinical
Molecular Formula: C16H27NO12
Molecular Weight: 425.39
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: COC(=O)[C@@H]1O[C@@H](OC)[C@@H](NC(C)=O)[C@@H](O)[C@@H]1O[C@@H]1O[C@@H](CO)[C@H](O)[C@H](O)[C@@H]1O
Standard InChI: InChI=1S/C16H27NO12/c1-5(19)17-7-9(21)12(13(14(24)25-2)29-15(7)26-3)28-16-11(23)10(22)8(20)6(4-18)27-16/h6-13,15-16,18,20-23H,4H2,1-3H3,(H,17,19)/t6-,7-,8-,9+,10-,11-,12-,13+,15+,16-/m0/s1
Standard InChI Key: HECHRIWYXUCCFQ-ZSRWQXKBSA-N
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Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
Molecule Type: Small molecule | 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: 425.39 | Molecular Weight (Monoisotopic): 425.1533 | AlogP: -4.42 | #Rotatable Bonds: 6 |
Polar Surface Area: 193.47 | Molecular Species: NEUTRAL | HBA: 12 | HBD: 6 |
#RO5 Violations: 2 | HBA (Lipinski): 13 | HBD (Lipinski): 6 | #RO5 Violations (Lipinski): 2 |
CX Acidic pKa: 11.88 | CX Basic pKa: | CX LogP: -3.88 | CX LogD: -3.88 |
Aromatic Rings: 0 | Heavy Atoms: 29 | QED Weighted: 0.22 | Np Likeness Score: 1.54 |
1. Galan MC, Dodson CS, Venot AP, Boons GJ.. (2004) Glycosyltransferase activity can be selectively modulated by chemical modifications of acceptor substrates., 14 (9): [PMID:15081009] [10.1016/j.bmcl.2004.02.024] |
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