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Details

Stereochemistry ACHIRAL
Molecular Formula C8H20NO4P
Molecular Weight 225.2225
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CGP-35348

SMILES

CCOC(OCC)P(O)(=O)CCCN

InChI

InChIKey=QIIVUOWTHWIXFO-UHFFFAOYSA-N
InChI=1S/C8H20NO4P/c1-3-12-8(13-4-2)14(10,11)7-5-6-9/h8H,3-7,9H2,1-2H3,(H,10,11)

HIDE SMILES / InChI

Molecular Formula C8H20NO4P
Molecular Weight 225.2225
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
27.0 nM [IC50]
PubMed

PubMed

TitleDatePubMed
GABAB receptor-positive modulators: enhancement of GABAB receptor agonist effects in vivo.
2010-10
Behavioral effects of gamma-hydroxybutyrate, its precursor gamma-butyrolactone, and GABA(B) receptor agonists: time course and differential antagonism by the GABA(B) receptor antagonist 3-aminopropyl(diethoxymethyl)phosphinic acid (CGP35348).
2009-09
Pharmacological and autoradiographic studies on the pathophysiological role of GABA(B) receptors in the dystonic hamster: pronounced antidystonic effects of baclofen after striatal injections.
2009-08-18
Comparative pharmacological activity of optical isomers of phenibut.
2008-03-31
Gamma-aminobutyric acidB (GABAB)-receptor mediation of different in vivo effects of gamma-butyrolactone.
2008-02
GABAB receptor blockade enhances theta and gamma rhythms in the hippocampus of behaving rats.
2007
Detection of gamma-aminobutyric acid-induced glutamate release in acute mouse hippocampal slices with a patch sensor.
2006-06-01
Discriminative stimulus effects of gamma-hydroxybutyrate: role of training dose.
2006-04
Discriminative stimulus effects of gamma-hydroxybutyrate in pigeons: role of diazepam-sensitive and -insensitive GABA(A) and GABA(B) receptors.
2004-03
Hindquarters vasoconstriction through central GABA(B) receptors in conscious rats.
2003-07
The GABAB receptor and recognition memory: possible modulation of its behavioral effects by the nitrergic system.
2003
Therapeutic intervention in mice deficient for succinate semialdehyde dehydrogenase (gamma-hydroxybutyric aciduria).
2002-07
International Union of Pharmacology. XXXIII. Mammalian gamma-aminobutyric acid(B) receptors: structure and function.
2002-06
GABA-B-related activity in processing of transcallosal response in cat motor cortex.
2002-05-15
The human GABA(B1b) and GABA(B2) heterodimeric recombinant receptor shows low sensitivity to phaclofen and saclofen.
2000-11
Expression cloning of GABA(B) receptors uncovers similarity to metabotropic glutamate receptors.
1997-03-20
CGP 35348 and CGP 55845A block the baclofen-induced depression of dorsal root evoked potentials in lumbar motoneurons of the neonatal rat.
1996-08-23
Characterization of the antiabsence effects of SCH 50911, a GABA-B receptor antagonist, in the lethargic mouse, gamma-hydroxybutyrate, and pentylenetetrazole models.
1995-09
Phosphinic acid analogues of GABA. 2. Selective, orally active GABAB antagonists.
1995-08-18
Antagonism of baclofen-induced depression of whole-cell synaptic currents in spinal dorsal horn neurones by the potent GABAB antagonist CGP55845.
1993-12
Reversal of scopolamine-induced amnesia by the GABAB receptor antagonist CGP 35348 in the mouse.
1993-04
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:57:22 GMT 2025
Edited
by admin
on Mon Mar 31 18:57:22 GMT 2025
Record UNII
87TI61875H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CGP-35348
Common Name English
3-AMINOPROPYL(DIETHOXYMETHYL)PHOSPHINIC ACID
Preferred Name English
Code System Code Type Description
CAS
123690-79-9
Created by admin on Mon Mar 31 18:57:22 GMT 2025 , Edited by admin on Mon Mar 31 18:57:22 GMT 2025
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EPA CompTox
DTXSID70154064
Created by admin on Mon Mar 31 18:57:22 GMT 2025 , Edited by admin on Mon Mar 31 18:57:22 GMT 2025
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FDA UNII
87TI61875H
Created by admin on Mon Mar 31 18:57:22 GMT 2025 , Edited by admin on Mon Mar 31 18:57:22 GMT 2025
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PUBCHEM
107699
Created by admin on Mon Mar 31 18:57:22 GMT 2025 , Edited by admin on Mon Mar 31 18:57:22 GMT 2025
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WIKIPEDIA
CGP-35348
Created by admin on Mon Mar 31 18:57:22 GMT 2025 , Edited by admin on Mon Mar 31 18:57:22 GMT 2025
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