Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
ID: ALA316871
Max Phase: Preclinical
Molecular Formula: C19H18N2O5
Molecular Weight: 354.36
Molecule Type: Small molecule
Associated Items:
ID: ALA316871
Max Phase: Preclinical
Molecular Formula: C19H18N2O5
Molecular Weight: 354.36
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: O=C(O)[C@@H](Cc1c[nH]c2ccccc12)N1C(=O)[C@@H]2[C@H](C1=O)[C@H]1CC[C@@H]2O1
Standard InChI: InChI=1S/C19H18N2O5/c22-17-15-13-5-6-14(26-13)16(15)18(23)21(17)12(19(24)25)7-9-8-20-11-4-2-1-3-10(9)11/h1-4,8,12-16,20H,5-7H2,(H,24,25)/t12-,13-,14+,15-,16+/m1/s1
Standard InChI Key: NXYMCEGDUWHVJR-LJIZCISZSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
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 |
---|
Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
---|
Molecular Weight: 354.36 | Molecular Weight (Monoisotopic): 354.1216 | AlogP: 1.33 | #Rotatable Bonds: 4 |
Polar Surface Area: 99.70 | Molecular Species: ACID | HBA: 4 | HBD: 2 |
#RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 3.79 | CX Basic pKa: | CX LogP: 1.24 | CX LogD: -2.03 |
Aromatic Rings: 2 | Heavy Atoms: 26 | QED Weighted: 0.81 | Np Likeness Score: 0.05 |
1. McCluskey A, Walkom C, Bowyer MC, Ackland SP, Gardiner E, Sakoff JA.. (2001) Cantharimides: a new class of modified cantharidin analogues inhibiting protein phosphatases 1 and 2A., 11 (22): [PMID:11677131] [10.1016/s0960-894x(01)00594-7] |
Source(1):