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HYRTIORETICULIN A ID: ALA2046768
Max Phase: Preclinical
Molecular Formula: C16H16N4O3
Molecular Weight: 312.33
Molecule Type: Small molecule
Associated Items:
Representations Synonyms (1): Hyrtioreticulin A Synonyms from Alternative Forms(1):
Canonical SMILES: O=C(O)[C@@H]1Cc2c([nH]c3ccc(O)cc23)[C@@H](Cc2c[nH]cn2)N1
Standard InChI: InChI=1S/C16H16N4O3/c21-9-1-2-12-10(4-9)11-5-14(16(22)23)19-13(15(11)20-12)3-8-6-17-7-18-8/h1-2,4,6-7,13-14,19-21H,3,5H2,(H,17,18)(H,22,23)/t13-,14+/m1/s1
Standard InChI Key: VXURZHPEJYLPGK-KGLIPLIRSA-N
Associated Targets(Human) Molecule Features Natural Product: YesOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: 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
Properties Molecular Weight: 312.33Molecular Weight (Monoisotopic): 312.1222AlogP: 1.48#Rotatable Bonds: 3Polar Surface Area: 114.03Molecular Species: ZWITTERIONHBA: 4HBD: 5#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 5#RO5 Violations (Lipinski): 0CX Acidic pKa: 1.53CX Basic pKa: 8.93CX LogP: -1.54CX LogD: -1.54Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.50Np Likeness Score: 0.86
References 1. Yamanokuchi R, Imada K, Miyazaki M, Kato H, Watanabe T, Fujimuro M, Saeki Y, Yoshinaga S, Terasawa H, Iwasaki N, Rotinsulu H, Losung F, Mangindaan RE, Namikoshi M, de Voogd NJ, Yokosawa H, Tsukamoto S.. (2012) Hyrtioreticulins A-E, indole alkaloids inhibiting the ubiquitin-activating enzyme, from the marine sponge Hyrtios reticulatus., 20 (14): [PMID:22695182 ] [10.1016/j.bmc.2012.05.044 ]