Acipimox

HCID 5310993CAS 51037-30-0

Grundinformationen

Standard-SMILES
Cc1cnc(C(=O)O)c[n+]1[O-]
InChIKey
DJQOOSBJCLSSEY-UHFFFAOYSA-N
Summenformel
C6H6N2O3
Durchschnittliche Molmasse
154,12 g/mol
Monoisotopische Masse
154,03784205

Überblick

5-methyl-4-oxido-2-pyrazin-4-iumcarboxylic acid is a pyrazinecarboxylic acid.

Namen und Bezeichner

Bevorzugter Name
Acipimox
IUPAC
5-methyl-4-oxidopyrazin-4-ium-2-carboxylic acid
Lokaler Name
Acipimox
Englischer Name
Acipimox
Summenformel
C6H6N2O3
Molmasse
154.12

Namen und Synonyme

ACIPIMOX51037-30-0OlbetamOlbemox5-methylpyrazine-2-carboxylic acid 4-oxide5-Methylpyrazinecarboxylic acid 4-oxide5-methyl-4-oxidopyrazin-4-ium-2-carboxylic acidDTXSID2046202NSC-759818K9AY9IR2SDDTXCID00262025-CARBOXY-2-METHYLPYRAZIN-1-IUM-1-OLATE
Weitere Namen anzeigen
K-9321AcimusAcipimox (K-9321)Acyclovir therapyAcipiMox-13C2,15N2Acipimox USP/EP/BPAcipimox - Bio-X ?
AcipimoxumRefChem:552678C10AD06256-928-35-Carboxy-2-methylpyrazine 1-oxideMFCD008657572-CARBOXY-5-METHYLPYRAZINE 4-OXIDEACIPIMOX [WHO-DD]

Datenbank-Bezeichner

CAS
51037-30-0
PubChem CID
5310993
DTXSID
DTXSID2046202
ChEMBL
CHEMBL345714
ChEBI
CHEBI:94688
UNII
K9AY9IR2SD
EC Number
256-928-3
Nikkaji
J10.290C

Eigenschaften

Berechnete Struktureigenschaften

XLogP
-1
Polarare Oberfläche (TPSA)
75,7 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
4
Frei drehbare Bindungen
1
Schwere Atome
11

Experimentelle und physikochemische Eigenschaften

Drugs · 2 Einträge

Pharmaceuticals -> Antilipidemics

Pharmaceuticals -> Listed in ZINC15

Physikochemische Eigenschaften

Schmelzpunkt
177 · 177-180 °C
Siedepunkt
539 · 539.0±45.0 °C(Predicted)
Dichte
1.44 · 1.44±0.1 g/cm3(Predicted)
storage temp.
2 · Inert atmosphere,2-8°C
Löslichkeit
Soluble in methanol, water (100 mM), DMSO (100 mM), ethanol (<1 mg/ml at 25° C), and 1 M NH4OH (1 mg/ml).
Aggregatzustand
Solid

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 5 Einträge

This chemical does not meet GHS hazard criteria for 41.7% (30 of 72) of reports.

Warning

H319 (58.3%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]

P264+P265, P280, P305+P351+P338, and P337+P317 (click each P-code to see the statement)

Aggregated GHS information provided per 72 reports by companies from 3 notifications to the ECHA C&L Inventory.

Gefahrenhinweise

Hazard Classes and CategoriesEye Irrit. 2A (58.3%)

Sicherheitsdaten

wgk
3
hs_code
2933.99.8290
RTECS-Nr.
UQ2453000
risk_code
36
Toxizität
LD50 orally in mice: 3500 mg/kg (Ambrogi)
hazard_code
Xi

Chemie und Industrie

Pharmakologische Informationen

ATC Code · 3 Einträge

C10AD06

C - Cardiovascular system

QC - Cardiovascular system

Mechanism of ActionAcipimox inhibits the production of triglycerides by the liver and the secretion of VLDL, which leads indirectly to a modest reduction in LDL and increase in HDL.
MeSH Pharmacological ClassificationSubstances that lower the levels of certain LIPIDS in the BLOOD. They are used to treat HYPERLIPIDEMIAS.
Anwendungen · 2 Einträge

BeschreibungAcipimox is a nicotinic acid derivate that structurally related to nicotinic acid. Like nicotinic acid, lowers lipids effectively, but unlike nicotinic acid, acipimox is longer acting and therefore much less prone to produce free fatty acid rebounding. It is usually employed in man in the therapy of hypertriglyceridemia. In addition to its lipid lowering activity, it produces a beneficial elevation of the anti-atherogenic high density lipoprotein subfraction, HDL2. Acipimox is recommended as a lipid-lowering agent to treat hyperlipidemia in patients with noninsulin dependent diabetes mellitus.

VerwendenAcipimox is a long-acting antilipemic agent and used for the treatment of hyperlipoproteinemias, in particular hypertriglyceridemias, and as adjunctive therapy for affecting cholesterol metabolism.

Darstellung · 1 Eintrag

synthetischeSynthesis of acipimox: Under cooling and stirring, 78 g of maleic anhydride was dissolved in a solution of 60 ml of chloroform, and 40 ml of 30% hydrogen peroxide was added. After 2 h, 4.8 g of 5-Methyl-2-pyrazinecarboxylic acid was added, and the temperature was kept at 0-5 °C for 2 d. The maleic acid was filtered off. Concentrate to a small volume, add ethyl acetate, and filter to obtain 1.1 g of acipimox, the melting point of which is 178-180 °C.

Anbieter50 Anbieter

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梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
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温州共赢化学有限公司+86-0086-577-64498589 +86-15355981851 · [email protected]
爱斯特(成都)生物制药股份有限公司+86-28-85122536 85324413 · [email protected]

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