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Rimonabant

CAS No.
168273-06-1
Chemical Name:
Rimonabant
Synonyms
A 281;xibuqum;ACOMPLIA;Sr 141716;rimobrant;Rimonaban;RIMONABANT;Limonabant;Unii-rml78en3xe;Rimonabant base
CBNumber:
CB4129374
Molecular Formula:
C22H21Cl3N4O
Molecular Weight:
463.79
MDL Number:
MFCD04034714
MOL File:
168273-06-1.mol
Last updated:2024-03-27 14:23:05

Rimonabant Properties

Melting point 154.7 °C
Density 1.41±0.1 g/cm3(Predicted)
storage temp. RT
solubility Soluble in DMSO (up to 20 mg/ml) or in Ethanol (up to 20 mg/ml).
pka 11.31±0.20(Predicted)
form solid
color White
Stability Stable for 1 year from date of purchase as supplied. Protect from moisture. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
CAS DataBase Reference 168273-06-1(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII RML78EN3XE
ATC code A08AX01

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS08,GHS09
Signal word  Danger
Hazard statements  H410-H372
Precautionary statements  P260-P264-P270-P314-P501-P273-P391-P501

Rimonabant price More Price(20)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 9000484 Rimonabant ≥98% 168273-06-1 5mg $46 2024-03-01 Buy
Cayman Chemical 9000484 Rimonabant ≥98% 168273-06-1 10mg $61 2024-03-01 Buy
Cayman Chemical 9000484 Rimonabant ≥98% 168273-06-1 25mg $138 2024-03-01 Buy
Cayman Chemical 9000484 Rimonabant ≥98% 168273-06-1 50mg $230 2024-03-01 Buy
ApexBio Technology B1429 Rimonabant 168273-06-1 10mM(in 1mL DMSO) $55 2021-12-16 Buy
Product number Packaging Price Buy
9000484 5mg $46 Buy
9000484 10mg $61 Buy
9000484 25mg $138 Buy
9000484 50mg $230 Buy
B1429 10mM(in 1mL DMSO) $55 Buy

Rimonabant Chemical Properties,Uses,Production

Description

Rimonabant is an inverse antagonist for the cannabinoid receptor (CB1). It acts by selectively blocking CB1 receptors found in the brain and in peripheral organs important in glucose and lipid metabolism, including adipose tissue, the liver, gastrointestinal tract, and muscle. Thus, rimonabant constitutes a therapeutic approach to obesity and cardiovascular risk factors. As an anorectic antiobesity drug, it was used as an adjunct to diet and exercise for obese or overweight patients with associated risk factors in Europe in 2006. Nevertheless, adverse effects including suicidality, depression, and anxiety were reported, based on which rimonadant was withdrawn worldwide in 2008.
Andogenous cannabinoids are related to the pleasurable effect of nicotine, rimonabant, as a cannabinoid receptor blocker, is also being tested as a potential anti-smoking treatment.

References

[1] https://www.drugs.com/acomplia.html
[2] Leite CE, Mocelin CA, Petersen GO, Leal MB, Thiesen FV (2009) Rimonabant: an antagonist drug of the endocannabinoid system for the treatment of obesity, Pharmacol Rep., 61, 217-224

Description

Rimonabant is a first-in-class drug launched as an oral treatment for obesity, and its mechanism of action involves the selective antagonism of cannabinoid type 1 (CB1) receptor. It is specifically indicated as an adjunct to diet and exercise for the treatment of obese patients (body mass index [BMI]≥30 kg/m2), or overweight patients (BMI>27 kg/m2) with associated risk factors such as type 2 diabetes or dyslipidemia. Additionally, rimonabant is currently under development as a treatment for nicotine dependence. The CB1 and CB2 receptors, along with their endogenous ligands, constitute the endocannabinoid system. The CB1 receptor is expressed in the brain, adipose tissue, and several peripheral organs; the CB2 receptor is predominantly expressed in immune cells. Activation of the CB1 receptor in the CNS is associated with appetite stimulation and the modulation of brain reward mechanism, whereas activation in the periphery favors metabolic processes that lead to hepatic lipogenesis and impaired glucose homeostasis. Rimonabant acts by selectively blocking the action of central and peripheral CB1 receptors, thereby reducing food intake and improving lipid and glucose metabolism.

Originator

Sanofi-Synthelabo (France)

Uses

Rimonabant is a selective antagonist of CB1 with IC50 of 13.6 nM and EC50 of 17.3 nM in hCB1 transfected HEK 293 membrane

Definition

ChEBI: Rimonabant is a carbohydrazide obtained by formal condensation of the carboxy group of 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxylic acid with the amino group of 1-aminopiperidine. It is a potent and selective cannabinoid receptor 1 (CB1R) antagonist. Besides its antagonistic properties, numerous studies have shown that, at micromolar concentrations rimonabant behaves as an inverse agonist at CB1 receptors. The drug was the first selective CB1 antagonist/inverse agonist introduced into clinical practice to treat obesity and metabolic-related disorders. It was later withdrawn from market due to CNS-related adverse effects including depression and suicidal ideation. It has a role as an anti-obesity agent, a CB1 receptor antagonist and an appetite depressant. It is a member of pyrazoles, a dichlorobenzene, a carbohydrazide, an amidopiperidine and a member of monochlorobenzenes.

brand name

Acomplia (Sanofi-Synthe-labo).

Synthesis

The reported preparation of rimonabant, both in small and large scale, is shown in the scheme. Lithium enolate formation of p-chlorophenyl ethyl ketone 54 with LiHMDS in THF at -78oC for 45 min followed by reaction with diethyl oxalate at -78oC and warming to room temperature over 16 h provided the lithium enolate salt of the diketoester 55. Reaction of diketoester salt 55 with 2,4-dichlorophenyl hydrazine (56) in ethanol at room temperature gave intermediate hydrazone 57 which is then cyclized in refluxing acetic acid for 24 h to obtain pyrazole ester 58. Hydrolysis of ester 58 with KOH in refluxing methanol:water mixture gave acid 59 which was then converted to the acid chloride 60 with thionyl chloride in refluxing toluene in very good yield. On scale, the synthesis of the acid chloride was performed in cyclohexane at 83oC. Reaction of acid chloride 60 with 1-aminopiperidine (61) in the presence of triethylamine at 0oC to room temperature over 3h gave rimonabant (VIII) which was isolated as the HCl salt by treating it with HCl in ether.

Synthesis_168273-06-1

References

1) Rinaldi-Carmona et al. (1994) SR141716A, a potent and selective antagonist of the brain cannabinoid receptor; FEBS Lett. 350 240 2) Rinaldi-Carmona et al. (1995) Biochemical and pharmacological characterization of SR141716A, the first potent and selective cannabinoid receptor antagonist; Life Sci. 56 1941

158681-13-1
168273-06-1
Synthesis of Rimonabant from Rimonabant hydrochloride

Rimonabant Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 262)Suppliers
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Hebei Mojin Biotechnology Co., Ltd
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18631714998 sales@czwytech.com CHINA 906 58

View Lastest Price from Rimonabant manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Rimonabant pictures 2024-04-25 Rimonabant
168273-06-1
US $100.00 / kg 1kg 99.9% 20tons Hong Kong Excellence Biotechnology Co., Ltd.
Rimonabant pictures 2024-04-12 Rimonabant
168273-06-1
US $3.00-1.00 / kg 1kg 99.9% 10 tons Shanghai Aosiris new Material Technology Co., LTD
Rimonabant pictures 2024-03-04 Rimonabant
168273-06-1
US $1.00 / g 1g 99.98% 50000 Doublewin Biological Technology Co., Ltd
  • Rimonabant pictures
  • Rimonabant
    168273-06-1
  • US $100.00 / kg
  • 99.9%
  • Hong Kong Excellence Biotechnology Co., Ltd.
  • Rimonabant pictures
  • Rimonabant
    168273-06-1
  • US $3.00-1.00 / kg
  • 99.9%
  • Shanghai Aosiris new Material Technology Co., LTD
  • Rimonabant pictures
  • Rimonabant
    168273-06-1
  • US $1.00 / g
  • 99.98%
  • Doublewin Biological Technology Co., Ltd

Rimonabant Spectrum

ACOMPLIA RIMONABANT RIMONABANT(ACOMPLIA,SR141716) 5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-N-piperidinopyrazole-3-carboxamide 1H-Pyrazole-3-carboxamide, 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-N-1-piperidinyl- 5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-N-1-piperidinyl-1H-pyrazole-3-carboxamide A 281 Sr 141716 Unii-rml78en3xe Rimonabant base ,99% N-(piperidin-1-yl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-Methyl-1H-pyrazole-3-carboxyaMide RiMonabant (SR141716) N-piperidino-5-(4-chlorophenyl)-1(2,4-dichlorophenyl)-4-Methyl-pyrazole-3-carboxaMide N-(Piperidin-1-yl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide hydrochloride Rimonabant(SR141716A) 158681-13-1 (HCl CAS) Rimonabant base 5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamid xibuqum Limonabant Rimonabant Powder rimobrant RimonabantQ: What is Rimonabant Q: What is the CAS Number of Rimonabant Q: What is the storage condition of Rimonabant Q: What are the applications of Rimonabant Rimonaban 168273-06-1 C22Cl3HN4O C22H21Cl3N4O SR141716 Weight Loss