Guanethidine sulfateProduct ingredient for Guanethidine

Name
Guanethidine sulfate
Drug Entry
Guanethidine

An antihypertensive agent that acts by inhibiting selectively transmission in post-ganglionic adrenergic nerves. It is believed to act mainly by preventing the release of norepinephrine at nerve endings and causes depletion of norepinephrine in peripheral sympathetic nerve terminals as well as in tissues. [PubChem]

Accession Number
DBSALT001861
Structure
Synonyms
(2-(Hexahydro-1(2H)-azocinyl)ethyl)guanidine sulfate (2:1) / Azocine, 1-(2-guanidinoethyl)octahydro-, sulfate (2:1) / beta-1-Azacyclooctylethylguanidine sulfate / Guanethidine bisulfate / Guanethidine sulphate / Guanidine, (2-(hexahydro-1(2H)-azocinyl)ethyl)-, sulfate (2:1) / Guanidine, (2-(octahydro-1-azocinyl)ethyl)-, hemisulfate
External IDs
SU-5864
UNII
8AQ60474G9
CAS Number
60-02-6
Weight
Average: 494.7
Monoisotopic: 494.336273167
Chemical Formula
C20H46N8O4S
InChI Key
NBJGGHFXCGHTNJ-UHFFFAOYSA-N
InChI
InChI=1S/2C10H22N4.H2O4S/c2*11-10(12)13-6-9-14-7-4-2-1-3-5-8-14;1-5(2,3)4/h2*1-9H2,(H4,11,12,13);(H2,1,2,3,4)
IUPAC Name
bis(N-[2-(azocan-1-yl)ethyl]guanidine); sulfuric acid
SMILES
OS(O)(=O)=O.NC(=N)NCCN1CCCCCCC1.NC(=N)NCCN1CCCCCCC1
KEGG Drug
D02237
ChemSpider
58812
ChEBI
51017
ChEMBL
CHEMBL2051958
Predicted Properties
PropertyValueSource
Water Solubility1.02 mg/mLALOGPS
logP0.78ALOGPS
logP0.8Chemaxon
logS-2.3ALOGPS
pKa (Strongest Basic)12.23Chemaxon
Physiological Charge2Chemaxon
Hydrogen Acceptor Count4Chemaxon
Hydrogen Donor Count3Chemaxon
Polar Surface Area65.14 Å2Chemaxon
Rotatable Bond Count6Chemaxon
Refractivity70 m3·mol-1Chemaxon
Polarizability23.78 Å3Chemaxon
Number of Rings2Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon