PHACLOFEN structure
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Common Name | PHACLOFEN | ||
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CAS Number | 114012-12-3 | Molecular Weight | 249.63100 | |
Density | 1.432 g/cm3 | Boiling Point | 467.1ºC at 760 mmHg | |
Molecular Formula | C9H13ClNO3P | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 236.3ºC | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of PHACLOFENPhaclofen is a selective GABAB receptor antagonist. Phaclofen is a peripheral and central baclofen antagonist. Phaclofen maybe a potential compound in determining the physiological significance of central and peripheral bicuculline-insensitive receptors with which GABA and (-)-baclofen interact[1][2]. |
Name | Phaclofen,(RS)-3-Amino-2-(4-chlorophenyl)propylphosphonicacid |
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Synonym | More Synonyms |
Description | Phaclofen is a selective GABAB receptor antagonist. Phaclofen is a peripheral and central baclofen antagonist. Phaclofen maybe a potential compound in determining the physiological significance of central and peripheral bicuculline-insensitive receptors with which GABA and (-)-baclofen interact[1][2]. |
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Related Catalog | |
Target |
GABAB receptor[1] |
In Vivo | Phaclofen (100 nmol; intrathecal injection) antagonizes the depressant effect of baclofen. Phaclofen (100 nmol) is devoid of stimulatory or depressant effects on spinal reflexes[3]. |
References |
Density | 1.432 g/cm3 |
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Boiling Point | 467.1ºC at 760 mmHg |
Molecular Formula | C9H13ClNO3P |
Molecular Weight | 249.63100 |
Flash Point | 236.3ºC |
Exact Mass | 249.03200 |
PSA | 93.36000 |
LogP | 2.26030 |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi: Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | 26-36 |
RIDADR | NONH for all modes of transport |
~% PHACLOFEN CAS#:114012-12-3 |
Literature: Hall Synthesis, 1989 , # 6 p. 442 - 443 |
~% PHACLOFEN CAS#:114012-12-3 |
Literature: Hall Synthesis, 1989 , # 6 p. 442 - 443 |
~% PHACLOFEN CAS#:114012-12-3 |
Literature: Chiefari, John; Galanopoulos, Speros; Janowski, Wit K.; Kerr, David I. B.; Prager, Rolf H. Australian Journal of Chemistry, 1987 , vol. 40, # 9 p. 1511 - 1518 |
~% PHACLOFEN CAS#:114012-12-3 |
Literature: Chiefari, John; Galanopoulos, Speros; Janowski, Wit K.; Kerr, David I. B.; Prager, Rolf H. Australian Journal of Chemistry, 1987 , vol. 40, # 9 p. 1511 - 1518 |
~% PHACLOFEN CAS#:114012-12-3 |
Literature: Chiefari, John; Galanopoulos, Speros; Janowski, Wit K.; Kerr, David I. B.; Prager, Rolf H. Australian Journal of Chemistry, 1987 , vol. 40, # 9 p. 1511 - 1518 |
Precursor 3 | |
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DownStream 0 |
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Transcriptome analysis of the key role of GAT2 gene in the hyper-accumulation of copper in the oyster Crassostrea angulata.
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The antinociceptive effect of stimulating the retrosplenial cortex in the rat tail-flick test but not in the formalin test involves the rostral anterior cingulate cortex.
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3-Amino-2-(4-chlorophenyl)propanephosphonic acid |
MFCD00069328 |