Shanghai Nianxing Industrial Co., Ltd
China
Product Name: Rilmenidine
Price:
Purity: 98.0%
Stocking Period: 10 Day
Contact: Yang

Shanghai Jizhi Biochemical Technology Co., Ltd
China
Product Name: Rilmenidine
Price: ￥1208.0/5mg ￥4938.0/25mg
Purity: 98.0%
Stocking Period: Inquiry
Contact: Liu jia

DC Chemicals Limited
China
Product Name: Rilmenidine
Price: $Inquiry/250mg $Inquiry/100mg $Inquiry/1g
Purity: 98.0%
Stocking Period: 3 Day
Contact: Tony Cao

Dayang Chem (Hangzhou) Co., Ltd.
China
Product Name: Rilmenidine
Price: $Inquiry/100g $Inquiry/1kg $Inquiry/100kg $Inquiry/1000kg
Purity: 98.0%
Stocking Period: Inquiry
Contact: Ms Wang

54187-04-1

54187-04-1 structure

Name: Rilmenidine
Chemical Name: N-(dicyclopropylmethyl)-4,5-dihydro-1,3-oxazol-2-amine
CAS Number: 54187-04-1
Molecular Formula: C₁₀H₁₆N₂O
Molecular Weight: 180.247
Catalog: API Circulatory system medication Antihypertensive drug
Create Date: 2018-07-25 17:37:37
Modify Date: 2024-01-02 17:36:24
Rilmenidine, an innovative antihypertensive agent, is an orally active, selective I1 imidazoline receptor agonist. Rilmenidine is an alpha 2-adrenoceptor agonist. Rilmenidine induces autophagy. Rilmenidine modulates proliferation and stimulates the proapoptotic protein Bax thus inducing the perturbation of the mitochondrial pathway and apoptosis in human leukemic K562 cells[1][2][3].

Name	N-(dicyclopropylmethyl)-4,5-dihydro-1,3-oxazol-2-amine
Synonyms	2-Oxazolamine, N-(dicyclopropylmethyl)-4,5-dihydro- Rilmenidine S 3341-3 S 3341 N-(Dicyclopropylmethyl)-4,5-dihydro-2-oxazolamine Oxaminozoline hyperium N-(Dicyclopropylmethyl)-4,5-dihydro-1,3-oxazol-2-amine 2-[N-(Dicyclopropylmethyl)amino]oxazoline EINECS 259-021-0 Tenaxum MFCD00865924

Description	Rilmenidine, an innovative antihypertensive agent, is an orally active, selective I1 imidazoline receptor agonist. Rilmenidine is an alpha 2-adrenoceptor agonist. Rilmenidine induces autophagy. Rilmenidine modulates proliferation and stimulates the proapoptotic protein Bax thus inducing the perturbation of the mitochondrial pathway and apoptosis in human leukemic K562 cells[1][2][3].
Related Catalog	Signaling Pathways >> Neuronal Signaling >> Imidazoline Receptor Signaling Pathways >> Apoptosis >> Apoptosis Research Areas >> Cardiovascular Disease Signaling Pathways >> GPCR/G Protein >> Imidazoline Receptor Signaling Pathways >> Autophagy >> Autophagy Signaling Pathways >> GPCR/G Protein >> Adrenergic Receptor
In Vitro	Rilmenidine (25-100 μM; 24 hours) inhibits K562 cell proliferation[2]. Cell Viability Assay[2] Cell Line: K562 cells Concentration: 25, 50, 100 μM Incubation Time: 24 hours Result: Dose-dependently inhibited K562 colony formation.
In Vivo	Rilmenidine-treated N171-82Q mice (i.p.; 4-times a week) displays significant improved forelimb grip strength and all limbs grip strength from 12 to 22 weeks of age[3].
References	[1]. Reid JL. Rilmenidine: a clinical overview. Am J Hypertens. 2000;13(6 Pt 2):106S-111S. [2]. Srdic-Rajic T, et al. Rilmenidine suppresses proliferation and promotes apoptosis via the mitochondrial pathway in human leukemic K562 cells. Eur J Pharm Sci. 2016;81:172-180. [3]. Rose C, et al. Rilmenidine attenuates toxicity of polyglutamine expansions in a mouse model of Huntington's disease. Hum Mol Genet. 2010;19(11):2144-2153.

Density	1.5±0.1 g/cm3
Boiling Point	355.5±9.0 °C at 760 mmHg
Melting Point	106 - 107ºC
Molecular Formula	C₁₀H₁₆N₂O
Molecular Weight	180.247
Flash Point	168.8±18.7 °C
Exact Mass	180.126266
PSA	33.62000
LogP	0.57
Vapour Pressure	0.0±0.8 mmHg at 25°C
Index of Refraction	1.711
Storage condition	Store at -20°C
Water Solubility	H2O: 7.3 mg/mL

CHEMICAL IDENTIFICATION

RTECS NUMBER :: RP7207400

CHEMICAL NAME :: Oxazolidine, 2-((dicyclopropylmethyl)imino)-

CAS REGISTRY NUMBER :: 54187-04-1

LAST UPDATED :: 199612

DATA ITEMS CITED :: 2

MOLECULAR FORMULA :: C10-H16-N2-O

MOLECULAR WEIGHT :: 180.28

WISWESSER LINE NOTATION :: T5N CO AUTJ BMY- AL3TJ&- AL3TJ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intravenous

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 24 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

MUTATION DATA

TYPE OF TEST :: Mutation in microorganisms

TEST SYSTEM :: Bacteria - Salmonella typhimurium

DOSE/DURATION :: 1 umol/plate

REFERENCE :: ENMUDM Environmental Mutagenesis. (New York, NY) V.1-9, 1979-87. For publisher information, see EMMUEG. Volume(issue)/page/year: 5,527,1983

Safety Phrases	S22-S24/25
WGK Germany	3
RTECS	RP7207400
HS Code	2934999090

Precursor 2
54187-44-9 54187-03-0
DownStream 0

HS Code	2934999090
Summary	2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

54187-04-1	54249-57-9
85047-14-9	85409-38-7
54187-44-9	207572-68-7
1158522-08-7	940364-43-2
1266541-83-6	134104-43-1
131615-57-1	6906-52-1
930439-75-1	1018584-77-4
1375289-11-4	849349-65-1