Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA3038258
Max Phase: Preclinical
Molecular Formula: C16H23N5Na3O18P3
Molecular Weight: 669.32
Molecule Type: Small molecule
Associated Items:
ID: ALA3038258
Max Phase: Preclinical
Molecular Formula: C16H23N5Na3O18P3
Molecular Weight: 669.32
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: C[C@@H]1O[C@H](OP(=O)([O-])OP(=O)([O-])OP(=O)([O-])OC[C@H]2O[C@@H](n3cnc4c(O)nc(N)nc43)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O.[Na+].[Na+].[Na+]
Standard InChI: InChI=1S/C16H26N5O18P3.3Na/c1-4-7(22)9(24)11(26)15(35-4)37-41(30,31)39-42(32,33)38-40(28,29)34-2-5-8(23)10(25)14(36-5)21-3-18-6-12(21)19-16(17)20-13(6)27;;;/h3-5,7-11,14-15,22-26H,2H2,1H3,(H,28,29)(H,30,31)(H,32,33)(H3,17,19,20,27);;;/q;3*+1/p-3/t4-,5+,7+,8+,9-,10+,11+,14+,15+;;;/m0.../s1
Standard InChI Key: WLMDSGQDMCFYTO-KVNJRFESSA-K
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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: 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: 669.32 | Molecular Weight (Monoisotopic): 669.0486 | AlogP: -3.07 | #Rotatable Bonds: 10 |
Polar Surface Area: 358.28 | Molecular Species: ACID | HBA: 20 | HBD: 10 |
#RO5 Violations: 3 | HBA (Lipinski): 23 | HBD (Lipinski): 11 | #RO5 Violations (Lipinski): 3 |
CX Acidic pKa: 0.88 | CX Basic pKa: 0.61 | CX LogP: -4.29 | CX LogD: -10.79 |
Aromatic Rings: 2 | Heavy Atoms: 42 | QED Weighted: 0.11 | Np Likeness Score: 1.21 |
1. Baisch G, Ohrlein R, Katopodis A. (1996) Enzymatic fucosylations with purine-diphosphate-fucoses (PDP-Fucoses), 6 (24): [10.1016/S0960-894X(96)00543-4] |
Source(1):