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KARAKOLINE

Product Name
KARAKOLINE
CAS No.
39089-30-0
Chemical Name
KARAKOLINE
Synonyms
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
Molecular Formula
C22H35NO4
Formula Weight
377.52
MOL File
39089-30-0.mol
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KARAKOLINE Property

Melting point:
185-186℃ (acetone )
Boiling point:
540.2±50.0 °C(Predicted)
Density 
1.30±0.1 g/cm3 (20 ºC 760 Torr)
storage temp. 
2-8°C
pka
13.80±0.70(Predicted)
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Safety

RTECS 
AR5569480
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
K139700
Product name
Karacoline
Packaging
1mg
Price
$140
Updated
2021/12/16
TRC
Product number
K139700
Product name
Karacoline
Packaging
10mg
Price
$580
Updated
2021/12/16
ApexBio Technology
Product number
N2030
Product name
Karacoline
Packaging
20mg
Price
$600
Updated
2021/12/16
ChemScene
Product number
CS-0027924
Product name
Karacoline
Packaging
10mg
Price
$743
Updated
2021/12/16
ChemScene
Product number
CS-0027924
Product name
Karacoline
Packaging
5mg
Price
$457
Updated
2021/12/16
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KARAKOLINE Chemical Properties,Usage,Production

Description

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.

Uses

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.

References

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

KARAKOLINE Preparation Products And Raw materials

Raw materials

Preparation Products

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KARAKOLINE Suppliers

ALB Technology Limited
Tel
702-983-3769
Fax
702-983-3769
Email
sales@albtechnology.com
Country
United States
ProdList
2993
Advantage
55
BOC Sciences
Tel
+1-631-485-4226
Fax
1-631-614-7828
Email
inquiry@bocsci.com
Country
United States
ProdList
19553
Advantage
58
Aladdin Scientific
Tel
+1-833-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
52927
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354
Email
support@targetmol.com
Country
United States
ProdList
19973
Advantage
58

39089-30-0, KARAKOLINERelated Search:


  • (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