Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA2348286
Max Phase: Preclinical
Molecular Formula: C16H17I2NO5S
Molecular Weight: 589.19
Molecule Type: Small molecule
Associated Items:
ID: ALA2348286
Max Phase: Preclinical
Molecular Formula: C16H17I2NO5S
Molecular Weight: 589.19
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CS(=O)(=O)N[C@H](CO)Cc1cc(I)c(Oc2ccc(O)cc2)c(I)c1
Standard InChI: InChI=1S/C16H17I2NO5S/c1-25(22,23)19-11(9-20)6-10-7-14(17)16(15(18)8-10)24-13-4-2-12(21)3-5-13/h2-5,7-8,11,19-21H,6,9H2,1H3/t11-/m0/s1
Standard InChI Key: BUEZCOGPQVGDGL-NSHDSACASA-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: 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: 589.19 | Molecular Weight (Monoisotopic): 588.8917 | AlogP: 2.85 | #Rotatable Bonds: 7 |
Polar Surface Area: 95.86 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 3 |
#RO5 Violations: 1 | HBA (Lipinski): 6 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: 9.58 | CX Basic pKa: | CX LogP: 3.13 | CX LogD: 3.12 |
Aromatic Rings: 2 | Heavy Atoms: 25 | QED Weighted: 0.43 | Np Likeness Score: -0.04 |
1. Actis M, Inoue A, Evison B, Perry S, Punchihewa C, Fujii N.. (2013) Small molecule inhibitors of PCNA/PIP-box interaction suppress translesion DNA synthesis., 21 (7): [PMID:23395113] [10.1016/j.bmc.2013.01.022] |
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