Ulodesine HydrochlorideProduct ingredient for Ulodesine

Name
Ulodesine Hydrochloride
Drug Entry
Ulodesine

Ulodesine has been used in trials studying the treatment of Gout, Arthritis, Hyperuricemia, and Joint Disease.

Accession Number
DBSALT002180
Structure
Synonyms
Not Available
UNII
O0JCK72YU4
CAS Number
615580-53-5
Weight
Average: 300.74
Monoisotopic: 300.0989181
Chemical Formula
C12H17ClN4O3
InChI Key
CMKFYLGNPVHLJV-RJUBDTSPSA-N
InChI
InChI=1S/C12H16N4O3.ClH/c17-5-8-3-16(4-9(8)18)2-7-1-13-11-10(7)14-6-15-12(11)19;/h1,6,8-9,13,17-18H,2-5H2,(H,14,15,19);1H/t8-,9+;/m1./s1
IUPAC Name
7-{[(3R,4R)-3-hydroxy-4-(hydroxymethyl)pyrrolidin-1-yl]methyl}-3H,4H,5H-pyrrolo[3,2-d]pyrimidin-4-one hydrochloride
SMILES
Cl.OC[C@H]1CN(CC2=CNC3=C2N=CNC3=O)C[C@@H]1O
ChemSpider
32700558
Predicted Properties
PropertyValueSource
Water Solubility1.72 mg/mLALOGPS
logP-1.1ALOGPS
logP-1.8Chemaxon
logS-2.2ALOGPS
pKa (Strongest Acidic)10.03Chemaxon
pKa (Strongest Basic)7.47Chemaxon
Physiological Charge1Chemaxon
Hydrogen Acceptor Count5Chemaxon
Hydrogen Donor Count4Chemaxon
Polar Surface Area100.95 Å2Chemaxon
Rotatable Bond Count3Chemaxon
Refractivity70.92 m3·mol-1Chemaxon
Polarizability26.28 Å3Chemaxon
Number of Rings3Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon