Nicorandil structure, CAS 65141-46-0

Nicorandil

CAS Number65141-46-0

SynonymsNitorubin; Perisalol; 2-(pyridine-3-carbonylamino)ethyl nitrate; 2-[(Pyridin-3-ylcarbonyl)amino]ethylnitrat; Nicorandil; Ikorel; SG-75; Dancor; EINECS 265-514-1; Nikoran; Nicorandilum; 2-[(Pyridin-3-ylcarbonyl)amino]ethyl nitrate; N-(2-hydroxyethyl)nicotinamide nitrate ester; 2-[(3-Pyridinylcarbonyl)amino]ethyl nitrate; Adancor; N-[2-(nitroxy)ethyl]-3-pyridine carboxamide; Sigmart; 2-Nicotinamidoethyl nitrate

Molecular FormulaC8H9N3O4

Molecular Weight211.17

Purity≥98 (HPLC)%

Density1.3±0.1 g/cm3

Boiling Point456.7±25.0 °C at 760 mmHg

Melting Point92ºC

Flash Point

Appearancepowder

EINECS265-514-1

MSDSChineseEnglish

SymbolTransport

Signal WordWarning

Cat. No.: 2A-9011644 Purity: ≥98 (HPLC)%
Change View

Please Login or Create an Account to: See VlP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

Quality Control of [ 65141-46-0 ] Purity: ≥98 (HPLC)% SDS Specification MoL

Chemical & Physical Properties
CAS Number65141-46-0
Catalog No.2A-9011644
Chinese Name尼可地尔
SynonymsNitorubin; Perisalol; 2-(pyridine-3-carbonylamino)ethyl nitrate; 2-[(Pyridin-3-ylcarbonyl)amino]ethylnitrat; Nicorandil; Ikorel; SG-75; Dancor; EINECS 265-514-1; Nikoran; Nicorandilum; 2-[(Pyridin-3-ylcarbonyl)amino]ethyl nitrate; N-(2-hydroxyethyl)nicotinamide nitrate ester; 2-[(3-Pyridinylcarbonyl)amino]ethyl nitrate; Adancor; N-[2-(nitroxy)ethyl]-3-pyridine carboxamide; Sigmart; 2-Nicotinamidoethyl nitrate
Molecular FormulaC8H9N3O4
Molecular Weight211.17
Purity≥98 (HPLC)
Density1.3±0.1 g/cm3
Boiling Point456.7±25.0 °C at 760 mmHg
Melting Point92ºC
Appearancepowder
Storage ConditionStore in an airtight container in a cool, dry plac
ApplicationNicorandil potassium channel activator.
EINECS265-514-1
HTC2933399090
PubChem ID329818637
MDL NumberMFCD00186520
SMILES[O-][N+](=O)OCCNC(=O)c1cccnc1
InChI1S/C8H9N3O4/c12-8(7-2-1-3-9-6-7)10-4-5-15-11(13)14/h1-3,6H,4-5H2,(H,10,12)
InChI KeyLBHIOVVIQHSOQN-UHFFFAOYSA-N
NACRES CodeNA.77
UNSPSC12352200
Hazard SymbolsTransport
MSDSmsds/11644_1_65141_46_0.pdf
BioactivityNicorandil is potassium channel activator.Target: Potassium ChannelNicorandil is a vasodilatory drug used to treat angina. Nicorandil stimulates guanylate cyclase to increase formation of cyclic GMP (cGMP). cGMP activates protein kinase G (PKG) which phosphorylates and inhibits GTPase RhoA and decreases Rho-kinase activity. Reduced Rho-kinase activity permits an increase in myosin phosphatase activity, decreasing the calcium sensitivity of the smooth muscle. PKG also activates the sarcolemma calcium pump to remove activating calcium. PKG acts on K+ channels to promote K+ efflux and the ensuing hyperpolarization inhibits voltage-gated calcium channels. Overall, this leads to relaxation of the smooth muscle and coronary vasodilation [1, 2]. Related Catalog Signaling Pathways >> Membrane Transporter/Ion Channel >> Potassium Channel Research Areas >> Cardiovascular Disease References [1]. Nakae, I., et al., Effects of intravenous nicorandil on coronary circulation in humans: plasma concentration and action mechanism. J Cardiovasc Pharmacol, 2000. 35(6): p. 919-25. [2]. Sauzeau, V., et al., Cyclic GMP-dependent protein kinase signaling pathway inhibits RhoA-induced Ca2+ sensitization of contraction in vascular smooth muscle. J Biol Chem, 2000. 275(28): p. 21722-9. Chemical & Physical Properties Density 1.3±0.1 g/cm3 Boiling Point 456.7±25.0 °C at 760 mmHg Melting Point 92ºC Molecular Formula C8H9N3O4 Molecular Weight 211.175 Flash Point 230.0±23.2 °C Exact Mass 211.059311 PSA 97.04000 LogP 0.72 Vapour Pressure 0.0±1.1 mmHg at 25°C Index of Refraction 1.548 InChIKey LBHIOVVIQHSOQN-UHFFFAOYSA-N SMILES O=C(NCCO[N+](=O)[O-])c1cccnc1 Storage condition 2-8°C
Use ofNicorandil is potassium channel activator.Target: Potassium ChannelNicorandil is a vasodilatory drug used to treat angina. Nicorandil stimulates guanylate cyclase to increase formation of cyclic GMP (cGMP). cGMP activates protein kinase G (PKG) which phosphorylates and inhibits GTPase RhoA and decreases Rho-kinase activity. Reduced Rho-kinase activity permits an increase in myosin phosphatase activity, decreasing the calcium sensitivity of the smooth muscle. PKG also activates the sarcolemma calcium pump to remove activating calcium. PKG acts on K+ channels to promote K+ efflux and the ensuing hyperpolarization inhibits voltage-gated calcium channels. Overall, this leads to relaxation of the smooth muscle and coronary vasodilation [1, 2]. Properties Articles51 Name nicorandil Synonym More Synonyms Nicorandil Biological Activity Description Nicorandil is potassium channel activator.Target: Potassium ChannelNicorandil is a vasodilatory drug used to treat angina. Nicorandil stimulates guanylate cyclase to increase formation of cyclic GMP (cGMP). cGMP activates protein kinase G (PKG) which phosphorylates and inhibits GTPase RhoA and decreases Rho-kinase activity. Reduced Rho-kinase activity permits an increase in myosin phosphatase activity, decreasing the calcium sensitivity of the smooth muscle. PKG also activates the sarcolemma calcium pump to remove activating calcium. PKG acts on K+ channels to promote K+ efflux and the ensuing hyperpolarization inhibits voltage-gated calcium channels. Overall, this leads to relaxation of the smooth muscle and coronary vasodilation [1, 2]. Related Catalog Signaling Pathways >> Membrane Transporter/Ion Channel >> Potassium Channel Research Areas >> Cardiovascular Disease References [1]. Nakae, I., et al., Effects of intravenous nicorandil on coronary circulation in humans: plasma concentration and action mechanism. J Cardiovasc Pharmacol, 2000. 35(6): p. 919-25. [2]. Sauzeau, V., et al., Cyclic GMP-dependent protein kinase signaling pathway inhibits RhoA-induced Ca2+ sensitization of contraction in vascular smooth muscle. J Biol Chem, 2000. 275(28): p. 21722-9. Chemical & Physical Properties Molecular Formula C8H9N3O4 Exact Mass 211.059311 PSA 97.04000 Index of Refraction 1.548 InChIKey LBHIOVVIQHSOQN-UHFFFAOYSA-N
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport InfoProduct name: Purity: 98.0%
MSDS Transport InfoModule 14. Shipping information 14.1 UN number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: No dangerous goods IMDG Code: No dangerous goods International Air Transport Dangerous Regulations: No dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special precautions for users No data available The company is not responsible for any damage caused by any operation or contact with the above products. For more terms of use, see invoice or package The reverse side of the mounting strip.
Related Products in Specialty Chemicals
Nicoclonate10571-59-22A-9011638
Nicodicodine808-24-22A-9011639
Nicofurate4397-91-52A-9011641
Nicomol27959-26-82A-9011642
Nicoracetam128326-80-72A-9011643
Nicotafuryl2A-3027292A-9011646
Nicotinanilide1752-96-12A-9011647
Nicotinyl hydroxamic acid5657-61-42A-9011648
Nicotredole29876-14-02A-9011649
Nictiazem95058-70-12A-9011650
Browse all Specialty Chemicals products »
Contact Us

Phone:

630-322-8886

630-322-8887

Email:

[email protected]

Office Locations:

Chicago, IL, USA

San Francisco, CA, USA