Free shipping on all orders over $ 500

6-Benzoylheteratisine

Cat. No. M39042
6-Benzoylheteratisine Structure
Size Price Availability Quantity
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

6-Benzoylheteratisine is a naturally occurring antagonist of the Na+ channel activator aconitine.

Chemical Information
Molecular Weight 495.61
Formula C29H37NO6
CAS Number 99759-48-5
Form Solid
Storage 4°C, protect from light
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Arash Salehi et al. Pharmaceuticals (Basel). Neuropharmacological Potential of Diterpenoid Alkaloids

[2] J F Heubach et al. Phytomedicine. 6-Benzoylheteratisine - a class-I antiarrhythmic substance from Aconitum tanguticum (Maxim.) Stapf

[3] U T Gutser et al. Neuropharmacology. The alkaloid 6-benzoylheteratisine inhibits voltage-gated Na+ channels in rat brain synaptosomes

[4] A Ameri. Neuropharmacology. Effects of the alkaloids 6-benzoylheteratisine and heteratisine on neuronal activity in rat hippocampal slices

[5] A Ameri. Naunyn Schmiedebergs Arch Pharmacol. Electrophysiological actions of the plant alkaloid 6-benzoylheteratisine in rat hippocampal slices

Related Sodium Channel Products
ASN008

ASN008 is a permanently positively charged sodium channel blocker.

Psalmotoxin 1

Psalmotoxin 1 (PcTx1) is a protein toxin that can bind at subunit-subunit interfaces of acid-sensing ion channel 1a (ASIC1a).

Jingzhaotoxin-III

Jingzhaotoxin-III is a potent and selective blocker of Nav1.5 channels, with an IC50 of 348 nM, and shows no effect on other sodium channel isoforms.

Huwentoxin-IV

Huwentoxin-IV is a potent and selective sodium channel blocker, inhibits neuronal Nav1.7, Nav1.2, Nav1.3 and Nav1.4 with IC50s of 26, 150, 338 and 400 nM, respectively.

Phrixotoxin 3

Phrixotoxin 3 is a potent blocker of voltage-gated sodium channels, with IC50s of 0.6, 42, 72, 288, 610 nM for NaV1.2, NaV1.3, NaV1.4, NaV1.1 and NaV1.5, respectively.

  Catalog
Abmole Inhibitor Catalog




Keywords: 6-Benzoylheteratisine supplier, Sodium Channel, inhibitors, activators


Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2023 AbMole BioScience. All Rights Reserved.