| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA3342260
Max Phase: Preclinical
Molecular Formula: C13H20NO7P
Molecular Weight: 333.28
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: COc1ccc(C(CCC(=O)N(C)O)P(=O)(O)O)cc1OC
Standard InChI: InChI=1S/C13H20NO7P/c1-14(16)13(15)7-6-12(22(17,18)19)9-4-5-10(20-2)11(8-9)21-3/h4-5,8,12,16H,6-7H2,1-3H3,(H2,17,18,19)
Standard InChI Key: MTKVPWZBCNHJJD-UHFFFAOYSA-N
Associated Targets(non-human)
1-deoxyxylulose-5-phosphate reductoisomerase 147 Activities
1-deoxy-D-xylulose 5-phosphate reductoisomerase 191 Activities
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Plasmodium falciparum 966862 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Molecule Features
| 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 |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 333.28 | Molecular Weight (Monoisotopic): 333.0977 | AlogP: 1.55 | #Rotatable Bonds: 7 |
| Polar Surface Area: 116.53 | Molecular Species: ACID | HBA: 5 | HBD: 3 |
| #RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 1.68 | CX Basic pKa: | CX LogP: -0.45 | CX LogD: -2.86 |
| Aromatic Rings: 1 | Heavy Atoms: 22 | QED Weighted: 0.39 | Np Likeness Score: 0.02 |
References
| 1. Konzuch S, Umeda T, Held J, Hähn S, Brücher K, Lienau C, Behrendt CT, Gräwert T, Bacher A, Illarionov B, Fischer M, Mordmüller B, Tanaka N, Kurz T.. (2014) Binding modes of reverse fosmidomycin analogs toward the antimalarial target IspC., 57 (21): [PMID:25254502] [10.1021/jm500850y] |
Source
Source(1):