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Molecule
ID:14027
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₁₀ClNO₂
Molecular Mass
163.6021
Exact Mass
163.04000625
Charge
0
InChI
InChI=1S/C6H9NO2.ClH/c8-6(9)5-1-3-7-4-2-5;/h1,7H,2-4H2,(H,8,9);1H
InChIKey
SUWREQRNTXCCBL-UHFFFAOYSA-N
Canonic Smiles
OC(=O)C1=CCNCC1.Cl
Isomeric Smiles
C1(=CCNCC1)C(=O)O.Cl
Calculated Properties
JChem
Acid pKa
4.3438463
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
-2.608818
LogD (pH = 7.4)
-2.5859718
Log P
-2.5858214
Molar Refractivity
33.7972
Polarizability
12.87252
Polar Surface Area
49.33
Rotatable Bonds
1
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
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RDKit
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JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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Synonyms
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IUPAC Traditional name
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IUPAC name
Registration numbers
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CAS Number
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MDL Number
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PubChem SID
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PubChem CID
Properties
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Safety Information
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Product Information
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Pharmacology Properties
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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Sigma Aldrich
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TRC
References
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PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
011532
MP Biomedicals
02153685
Sigma Aldrich
G002
TRC
I819560
Academic Data
PubChem
155107
Names and Identifiers
Synonyms
1,2,3,6-Tetrahydro-pyridine-4-carboxylic acid hydrochloride
1,2,3,6-Tetrahydro-4-pyridinecarboxylic acid hydrochloride
Isoguvacine hydrochloride
1,2,5,6,-Tetrahydroisonicotinic acid Hydrochloride
ISOGUVACINE
Iso Guvacine Hydrochloride
IUPAC Traditional name
isoguvacine hydrochloride
IUPAC name
1,2,3,6-tetrahydropyridine-4-carboxylic acid hydrochloride
Registration numbers
CAS Number
64603-90-3
68547-97-7
MDL Number
MFCD00055192
PubChem SID
24278160
160977334
PubChem CID
155107
Properties
Safety Information
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
TSCA Listed
false
Source
Storage Condition
Room Temperature (15-30°C)
Source
German water hazard class
3
Source
Safety Statements
26
-
36
Source
European Hazard Symbols
Irritant (Xi)
Source
Risk Statements
36/37/38
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
GHS Signal Word
Warning
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Product Information
Certificate of Analysis
Download link
Source
Download link
Source
Pharmacology Properties
Gene Information
human ... GABRA1(2554), GABRA2(2555), GABRA3(2556), GABRA4(2557), GABRA5(2558), GABRA6(2559), GABRB1(2560), GABRB2(2561), GABRB3(2562)
Source
Physical Property
Solubility
methanol: slightly soluble
Source
neutral and acidic solutions: stable (in basic solutions the free amine can oxidize easily)
Source
H2O: soluble (refrigerate if not used immediately.)
Source
Apperance
white solid
Source
Molecule Details
MP Biomedicals
02153685
Hydrochloride
GABA agonist
Sigma Aldrich
G002
Biochem/physiol Actions
GABAA receptor agonist.
TRC
I819560
A GABAA receptor agonist. Anticonvulsant; antiepileptic.
References
PubChem Literature
From Data Sources
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Falch, E., et al.: J. Med. Chem., 24, 285 (1981)
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Bain, J., et al.: Biochem. J., 408, 297 (1981)
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Kennedy, H., et al.: J. Biol. Chem., 274, 13281 (1981)
Bioactivity
PubChem BioAssay