FAUC 213

Product Name
FAUC 213
CAS No.
337972-47-1
Chemical Name
FAUC 213
Synonyms
FAUC213 FAUC-213;Pyrazolo[1,5-a]pyridine, 2-[[4-(4-chlorophenyl)-1-piperazinyl]methyl]-;inhibit,p5-HT2,FAUC 213,orally,pα1,BBB,AMPH,barrier,amphetamin,blood-brain,Inhibitor,Dopamine Receptor,p5-HT1,antipsychotic
CBNumber
CB8503491
Molecular Formula
C18H19ClN4
Formula Weight
326.82
MOL File
337972-47-1.mol
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FAUC 213 Property

storage temp. 
2-8°C
solubility 
DMSO: ~24 mg/mL with warming up to 60°C
form 
solid
color 
white
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
F101068
Product name
FAUC 213
Packaging
5mg
Price
$130
Updated
2021/12/16
TRC
Product number
F101068
Product name
FAUC 213
Packaging
10mg
Price
$200
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0002679
Product name
FAUC 213
Purity
95.00%
Packaging
5MG
Price
$765.48
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0002679
Product name
FAUC 213
Purity
95.00%
Packaging
25MG
Price
$1286.73
Updated
2021/12/16
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FAUC 213 Chemical Properties,Usage,Production

Uses

FAUC 213 is a highly selective D4 dopamine receptor full antagonist.

in vivo

FAUC 213 (7.5-30 mg/kg; orally; single dose) significantly reduces this elevation in AMPH-induced locomotor hyper-activity only pre-treatment with 30 mg/kg. FAUC 213 significantly restores the prepulse inhibition (PPI) reduction caused by the apomorphine (APO) treatment with 30 mg/kg[1].

Animal Model:Male adult Wistar rats weighing 300-350 g[1]
Dosage:7.5, 15, 30 mg/kg
Administration:Orally; single dose
Result:Significantly reduced this elevation in amphetamin (AMPH)-induced locomotor hyper-activity only pre-treatment with 30 mg/kg.

IC 50

hD4.4 Receptor: 2.2 nM (Ki); hD2 Receptor: 3.4 μM (Ki); hD3 Receptor: 5.3 μM (Ki)

FAUC 213 Preparation Products And Raw materials

Raw materials

Preparation Products

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FAUC 213 Suppliers

China 30 India 1 Switzerland 1 United States 4 Global 36
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9803
Advantage
58
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
71826
Advantage
60
ShangHai Biochempartner Co.,Ltd
Tel
177-54423994 17754423994
Fax
QQ:2853530913
Email
2853530910@QQ.com
Country
China
ProdList
8000
Advantage
62
Shanghai Chaolan Chemical Technology Center
Tel
021-QQ：65489617 15618227136
Fax
21-5161 9052
Email
Sales@ATKchemical.com
Country
China
ProdList
9125
Advantage
58
Chuzhou KeMail Chemical Technology Co., Ltd
Tel
0550-5196001 15000891977
Fax
0550-5196001
Email
wj520wjxby@126.com
Country
China
ProdList
1944
Advantage
55
TargetMol Chemicals Inc.
Tel
+1-781-999-5354; +17819995354
Email
marketing@targetmol.com
Country
United States
ProdList
32435
Advantage
58
Zhejiang J&C Biological Technology Co.,Limited
Tel
+1-2135480471
Email
sales@sarms4muscle.com
Country
China
ProdList
10473
Advantage
58
Suzhou Chenrui Biotechnology Co. LTD
Tel
17625585511
Fax
qq：1580084073
Email
1580084073@qq.com
Country
China
ProdList
960
Advantage
58
ShangHai ChuanQian Chemcial Technique Centre
Tel
15869524721
Email
3525679403@qq.com
Country
China
ProdList
4989
Advantage
58
Energy Chemical
Tel
021-58432009 400-005-6266
Fax
021-58436166
Email
marketing@energy-chemical.com
Country
China
ProdList
44918
Advantage
58

337972-47-1, FAUC 213Related Search:

FAUC 213 C-PYRAZOLO[1,5-A]PYRIDIN-2-YL-METHYLAMINE

  • Pyrazolo[1,5-a]pyridine, 2-[[4-(4-chlorophenyl)-1-piperazinyl]methyl]-
  • inhibit,p5-HT2,FAUC 213,orally,pα1,BBB,AMPH,barrier,amphetamin,blood-brain,Inhibitor,Dopamine Receptor,p5-HT1,antipsychotic
  • FAUC213 FAUC-213
  • 337972-47-1