KARAKOLINE

KARAKOLINE Struktur
39089-30-0
CAS-Nr.
39089-30-0
Englisch Name:
KARAKOLINE
Synonyma:
Karacoline;Carmicheline(7CI);Inhibitor,Karacoline,inhibit;(16S)-20-Ethyl-16-methoxy-4-methylaconitane-1α,8,14α-triol;(1α,14α,16β)-20-Ethyl-16-methoxy-4-methylaconitane-1,8,14-triol;Aconitane-1,8,14-triol,20-ethyl-16-methoxy-4-methyl-, (1a,14a,16b)-;Aconitane-1,8,14-triol, 20-ethyl-16-methoxy-4-methyl-, (1α,14α,16β)-;11aH-12,3,6a-Ethanylylidene-7,9-methanonaphth[2,3-b]azocine, aconitane-1,8,14-triolderiv.
CBNumber:
CB3986952
Summenformel:
C22H35NO4
Molgewicht:
377.52
MOL-Datei:
39089-30-0.mol

KARAKOLINE Eigenschaften

Schmelzpunkt:
185-186℃ (acetone )
Siedepunkt:
540.2±50.0 °C(Predicted)
Dichte
1.30±0.1 g/cm3 (20 ºC 760 Torr)
storage temp. 
2-8°C
pka
13.80±0.70(Predicted)

Sicherheit

RTECS-Nr. AR5569480

KARAKOLINE Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

A second atisine base found in the tubers of Aconitum karacolicum, the structure has been elucidated from chemical and spectroscopic data. Oxidation with KMn04 gives anhydroepoxykaracoline. The alkaloid furnishes a triacetyl deriva_x0002_tive which, after pyrolysis and hydrolysis, yields acetyldemethylisopyrokaracoline.

Verwenden

Karacoline is an Aconitane (A189875) derivative, which is a neurotoxin which activates tetrodotoxin-sensitive Na+ channels, inducing presynaptic depolarization, thus blocking the nerve action potential which, in turn, blocks the release of neurotransmitters and decreases the end plate potential at the neuromuscular junction.

Definition

ChEBI: An organonitrogen heterocyclic compound that is aconitane bearing hydroxy groups at the 1alpha, 8, and 14alpha positions and substituted at on the nitrogen and at positions 4 and 16beta by ethyl, methyl, a d methoxy groups, respectively.

Einzelnachweise

Sultankhodzhaev, Yunusov, Yunusov., Khim. Prir. Soedin., 9, 199 (1973)

KARAKOLINE Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


KARAKOLINE Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 68)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Chengdu GLP biotechnology Co Ltd
028-87075086 13350802083
scglp@glp-china.com CHINA 1824 58
Chengdu Biopurify Phytochemicals Ltd.
+8618080483897
sales@biopurify.com China 3424 58
Shaanxi Pioneer Biotech Co., Ltd .
+8613259417953
sales@pioneerbiotech.com China 3000 58
BOC Sciences
+1-631-485-4226
inquiry@bocsci.com United States 19553 58
Neostar United (Changzhou) Industrial Co., Ltd.
+86-519-519-85557386
marketing1@neostarunited.com China 8349 58
Wuhan ChemNorm Biotech Co.,Ltd.
+86-27-8439 4403 18971486879
sales@chemnorm.com CHINA 2935 58
Hubei Ipure Biology Co., Ltd
+8613367258412
ada@ipurechemical.com China 10326 58
Chengdu Youngshe Chemical Co., Ltd.
+8618108235634
Cecilia@youngshechem.com China 2345 58
TargetMol Chemicals Inc.
+1-781-999-5354
support@targetmol.com United States 19973 58
ShenZhen Trendseen Biological Technology Co.,Ltd.
13417589054
trendseenbio@gmail.com China 11681 58

39089-30-0()Verwandte Suche:


  • (16S)-20-Ethyl-16-methoxy-4-methylaconitane-1α,8,14α-triol
  • Karacoline
  • Aconitane-1,8,14-triol,20-ethyl-16-methoxy-4-methyl-, (1a,14a,16b)-
  • Aconitane-1,8,14-triol, 20-ethyl-16-methoxy-4-methyl-, (1α,14α,16β)-
  • Carmicheline(7CI)
  • 11aH-12,3,6a-Ethanylylidene-7,9-methanonaphth[2,3-b]azocine, aconitane-1,8,14-triolderiv.
  • (1α,14α,16β)-20-Ethyl-16-methoxy-4-methylaconitane-1,8,14-triol
  • Inhibitor,Karacoline,inhibit
  • 39089-30-0
  • Alkaloids
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
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