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A8001

Aconitin

≥95% (HPLC), fibronectin binding Inhibitor , crystalline

Synonym(e):

Acetylbenzoylaconin

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PackungsgrößeSKUVerfügbarkeitPreis
5 mg
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€ 31,10
25 mg
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€ 128,00
100 mg
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€ 342,00
250 mg
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€ 682,00
€ 579,70

Über diesen Artikel

Empirische Formel (Hill-System):
C34H47NO11
CAS-Nummer:
Molekulargewicht:
645.74
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
206-121-7
MDL number:
Beilstein/REAXYS Number:
74608
Assay:
≥95% (HPLC)
Form:
crystalline
Quality level:

€ 31,10


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Produktname

Aconitin, ≥95% (HPLC), crystalline

Quality Level

assay

≥95% (HPLC)

form

crystalline

color

white

solubility

H2O: 0.3 mg/mL, ethanol: 35 mg/mL

SMILES string

CCN1C[C@]2(COC)[C@H](O)C[C@@H](OC)C34C5C[C@]6(O)[C@@H](OC)[C@H](O)[C@@](OC(C)=O)(C5[C@H]6OC(=O)c7ccccc7)C([C@H](OC)C23)C14

InChI

1S/C34H47NO11/c1-7-35-15-31(16-41-3)20(37)13-21(42-4)33-19-14-32(40)28(45-30(39)18-11-9-8-10-12-18)22(19)34(46-17(2)36,27(38)29(32)44-6)23(26(33)35)24(43-5)25(31)33/h8-12,19-29,37-38,40H,7,13-16H2,1-6H3/t19-,20-,21-,22-,23+,24+,25?,26?,27+,28-,29+,31+,32-,33?,34-/m1/s1

InChI key

XFSBVAOIAHNAPC-VBUFWTEXSA-N

Application

Aconitine is a neurotoxin which activates tetrodotoxin-sensitive Na+ channels, inducing presynaptic depolarization and blocking the release of neurotransmitters. Aconitine also blocks norepinephrine reuptake. In the heart, aconitine induces ventricular tachycardia after intracoronary injection.
Aconitine has been used:
  • to study its cardiotoxic effects along the pericardium meridian (PM) on cardiac rhythm in rabbits[1]
  • as a standard in high-performance thin layer chromatography (HPTLC) fingerprinting method
  • in the aconitine-based lipo-alkaloids semi-synthesis[2]

Biochem/physiol Actions

Neurotoxin. 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. Aconitine also blocks norepinephrine reuptake. In the heart, aconitine induces ventricular tachycardia after intracoronary injection. In cultured ventricular myocytes, aconitine increases the duration of the action potential and induces the appearance of early after depolarization.
Aconitine is a diesterditerpene alkaloid found abundantly in the plant Aconitum genera.[3] It possesses analgesic, antipyretic and antirheumatic activity. Aconitine is involved in blocking neurotransmission. It acts as a neurotoxin as well as a cardiotoxin. Aconitine triggers ventricular tachycardia (VT) and ventricular fibrillation (VF). It interacts with voltage-dependent Na+ channels which results in the depolarization of membranes.[4] Aconitine may exhibit therapeutic effects against systemic lupus erythematosus (SLE).[5] It also inhibits the reuptake of norepinephrine.

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PHL89376

Aconitine

assay

≥95% (HPLC)

assay

≥95.0% (HPLC)

assay

≥98% (titration)

assay

≥95.0% (HPLC)

form

crystalline

form

-

form

crystalline

form

-

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

-

solubility

H2O: 0.3 mg/mL, ethanol: 35 mg/mL

solubility

-

solubility

H2O: 1 g/mL, ethanol: 20 mg/mL

solubility

-

color

white

color

-

color

white

color

-


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pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 1 Oral - Acute Tox. 2 Inhalation

Lagerklasse

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges



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Ling Ye et al.
Toxicology letters, 216(2-3), 86-99 (2012-12-04)
Aconitum alkaloids including aconitine (AC), mesaconitine (MA), hypaconitine (HA), are highly toxic. Their hydrolysates, such as benzoylaconine (BAC), benzoylmesaconine (BMA), benzoylhypaconine (BHA), aconine, and mesaconine, are considerably less toxic. Efflux transporters, including P-glycoprotein (P-gp), breast cancer resistance protein (BCRP), and
Bio-analytical studies on the process of detoxification and safety evaluation of Aconitum laciniatum and Abrus precatorius for use in ayurvedic preparations
Bapat, S P and Sane, R T
International Journal of Pharmaceutical Sciences and Research, 3(3), 914-914 (2012)
Peijian Tong et al.
Journal of ethnopharmacology, 146(2), 562-571 (2013-02-05)
Fuzi (lateral root of Aconitum carmichaeli) is a popular traditional Chinese medicine well known for its both therapeutic and high-toxic activities. Its toxic alkaloid ingredients, mainly aconitine, mesaconitine, and hypaconitine, are responsible for the high toxicity. However, to date, no



Global Trade Item Number

SKUGTIN
A8001-5MG04061833390948
A8001-250MG04061832569178
A8001-100MG04061832569161
A8001-25MG04061833390931

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