Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
ID: ALA3339156
Max Phase: Preclinical
Molecular Formula: C30H38O4
Molecular Weight: 462.63
Molecule Type: Small molecule
Associated Items:
ID: ALA3339156
Max Phase: Preclinical
Molecular Formula: C30H38O4
Molecular Weight: 462.63
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CC(C)=CCC[C@@H](C)[C@@H]1C=C[C@]2(C(=O)O)[C@@H](CC(C)=C[C@H]2/C=C(\C)c2ccc(C(=O)O)cc2)C1
Standard InChI: InChI=1S/C30H38O4/c1-19(2)7-6-8-21(4)25-13-14-30(29(33)34)26(15-20(3)16-27(30)18-25)17-22(5)23-9-11-24(12-10-23)28(31)32/h7,9-15,17,21,25-27H,6,8,16,18H2,1-5H3,(H,31,32)(H,33,34)/b22-17+/t21-,25-,26+,27+,30-/m1/s1
Standard InChI Key: YEQLBOWLDTXBBB-VVBJMDLTSA-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: 462.63 | Molecular Weight (Monoisotopic): 462.2770 | AlogP: 7.40 | #Rotatable Bonds: 8 |
Polar Surface Area: 74.60 | Molecular Species: ACID | HBA: 2 | HBD: 2 |
#RO5 Violations: 1 | HBA (Lipinski): 4 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: 3.95 | CX Basic pKa: | CX LogP: 7.34 | CX LogD: 1.57 |
Aromatic Rings: 1 | Heavy Atoms: 34 | QED Weighted: 0.39 | Np Likeness Score: 2.05 |
1. Desrat S, Pujals A, Colas C, Dardenne J, Gény C, Favre L, Dumontet V, Iorga BI, Litaudon M, Raphaël M, Wiels J, Roussi F.. (2014) Pro-apoptotic meiogynin A derivatives that target Bcl-xL and Mcl-1., 24 (21): [PMID:25266781] [10.1016/j.bmcl.2014.09.004] |
2. Negi A, Murphy PV.. (2021) Development of Mcl-1 inhibitors for cancer therapy., 210 [PMID:33333396] [10.1016/j.ejmech.2020.113038] |
Source(1):