Welcome to LookChem.com Sign In|Join Free

CAS

  • or

826-39-1

Post Buying Request

826-39-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

826-39-1 Usage

Description

Mecamylamine hydrochloride is a non-competitive nicotinic acetylcholine receptor antagonist with preferential activity at the α3β4 subtype (IC50 = 90-640 nM) compared to α4β2, α3β2, and α7 subtypes (IC50 range from 1-7 μM), previously used to treat hypertension.Displays antidepressant-like effects in mice.Mecamylamine HCl is supplied as tablets for oral use, each containing 2.5 mg mecamylamine HCl. Inactive ingredients are calcium phosphate, D&C Yellow 10, FD&C Yellow 6, lactose, magnesium stearate, cornstarch, and talc.

Chemical Properties

Mecamylamine hydrochloride is a white, odorless, or practically odorless, crystalline powder, is highly stable, soluble in water and has a molecular weight of 203.75.

Uses

Different sources of media describe the Uses of 826-39-1 differently. You can refer to the following data:
1. Mecamylamine hydrochloride has been used as an additive in extracellular saline during current-clamp recordings to reduce synaptic input. It has also been used as a non-selective nicotinic acetyl choline receptor blocker in aortic body neurons and in MLO-Y4 cells.
2. Mecamylamine is a noncompetitive nicotinic acetylcholine receptor antagonist with preferential activity at the α3β4 subtype (IC50 = 90-640 nM) compared to α4β2, α3β2, and α7 subtypes (IC50s range from 1-7 μM). Mecamylamine is widely used as a broad-spectrum antagonist of neuronal nicotinic acetylcholine receptors in basic nicotine research. It has been reported to be effective as an aid to smoking cessation and may also be of use in various nicotine-responsive, neuropsychiatric disorders.[Cayman Chemical]
3. A noncompetitive nicotinic AChR inhibitor.

Therapeutic Function

Antihypertensive

General Description

The secondary aminemecamylamine hydrochloride, N,2,3,3-tetramethyl-2-norbornanaminehydrochloride (Inversine), has a powerful ganglionicblocking effect that is almost identical to that ofhexamethonium. It has an advantage over most of the ganglionicblocking agents in being absorbed readily andsmoothly from the GI tract. It is rarely used, however, forthe treatment of moderate-to-severe hypertension becausesevere orthostatic hypotension occurs when the drug blockssympathetic ganglia.

Biological Activity

Non-competitive nicotinic acetylcholine receptor antagonist. Displays antidepressant-like effects in mice.

Biochem/physiol Actions

Noncompetitive nicotinic acetylcholine receptor antagonist; preferentially blocks nicotinic receptors at autonomic ganglia; crosses blood-brain barrier.

Metabolism

Mecamylamine hydrochloride (Inversine) is a secondary amine and can therefore easily penetrate cell membranes. Its absorption from the gastrointestinal tract is more complete than that of the quaternary ammonium compounds. Mecamylamine is well absorbed orally and crosses both the blood-brain and placental barriers; its distribution is not confined to the extracellular space. High concentrations of the drug accumulate in the liver and kidney, and it is excreted unchanged by the kidney. In contrast to most of the highly ionized ganglionic blocking agents, mecamylamine can produce central nervous system effects, including tremors, mental confusion, seizures, mania, and depression.The mechanism by which these central effects are produced is unclear.Mecamylamine is rarely used today as an antihypertensive drug because it blocks both parasympathetic and sympathetic ganglia.

Check Digit Verification of cas no

The CAS Registry Mumber 826-39-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 826-39:
(5*8)+(4*2)+(3*6)+(2*3)+(1*9)=81
81 % 10 = 1
So 826-39-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H21N.ClH/c1-10(2)8-5-6-9(7-8)11(10,3)12-4;/h8-9,12H,5-7H2,1-4H3;1H

826-39-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • USP

  • (1376006)  Mecamylamine hydrochloride  United States Pharmacopeia (USP) Reference Standard

  • 826-39-1

  • 1376006-200MG

  • 4,588.74CNY

  • Detail
  • Sigma

  • (M9020)  Mecamylamine hydrochloride  

  • 826-39-1

  • M9020-5MG

  • 537.03CNY

  • Detail
  • Sigma

  • (M9020)  Mecamylamine hydrochloride  

  • 826-39-1

  • M9020-25MG

  • 2,165.67CNY

  • Detail
  • Sigma

  • (M9020)  Mecamylamine hydrochloride  

  • 826-39-1

  • M9020-100MG

  • 6,546.15CNY

  • Detail

826-39-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Mecamylamine Hydrochloride

1.2 Other means of identification

Product number -
Other names Bicyclo[2.2.1]heptan-2-amine, N,2,3,3-tetramethyl-, hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:826-39-1 SDS

826-39-1Synthetic route

(+/-)-exo-mecamylamine hydrochloride
826-39-1

(+/-)-exo-mecamylamine hydrochloride

(S)-phenylethyl isocyanate
14649-03-7

(S)-phenylethyl isocyanate

A

(1S,2R,4R)-N-<((S)-1-phenylethyl)carbamoyl>mecamylamine

(1S,2R,4R)-N-<((S)-1-phenylethyl)carbamoyl>mecamylamine

B

(1R,2R,4S)-N-<((S)-1-phenylethyl)carbamoyl>mecamylamine
107485-87-0

(1R,2R,4S)-N-<((S)-1-phenylethyl)carbamoyl>mecamylamine

Conditions
ConditionsYield
With sodium carbonate 2.) CHCl3, 1 h, room t.; Yield given. Multistep reaction. Yields of byproduct given;
ethyl bromide
74-96-4

ethyl bromide

(+/-)-exo-mecamylamine hydrochloride
826-39-1

(+/-)-exo-mecamylamine hydrochloride

N-ethyl mecamylamine

N-ethyl mecamylamine

Conditions
ConditionsYield
With potassium hydrogencarbonate In tetrahydrofuran; N,N-dimethyl-formamide Alkylation; Heating;
(+/-)-exo-mecamylamine hydrochloride
826-39-1

(+/-)-exo-mecamylamine hydrochloride

benzyl chloride
100-44-7

benzyl chloride

N-benzyl mecamylamine

N-benzyl mecamylamine

Conditions
ConditionsYield
With potassium hydrogencarbonate In tetrahydrofuran; N,N-dimethyl-formamide Alkylation; Heating;
(+/-)-exo-mecamylamine hydrochloride
826-39-1

(+/-)-exo-mecamylamine hydrochloride

cyclopropylcarbinyl bromide
7051-34-5

cyclopropylcarbinyl bromide

N-cyclopropylmethyl mecamylamine

N-cyclopropylmethyl mecamylamine

Conditions
ConditionsYield
With potassium hydrogencarbonate In tetrahydrofuran; N,N-dimethyl-formamide Alkylation; Heating;
(+/-)-exo-mecamylamine hydrochloride
826-39-1

(+/-)-exo-mecamylamine hydrochloride

allyl bromide
106-95-6

allyl bromide

N-allyl mecamylamine

N-allyl mecamylamine

Conditions
ConditionsYield
With potassium hydrogencarbonate In tetrahydrofuran; N,N-dimethyl-formamide Alkylation; Heating;
(+/-)-exo-mecamylamine hydrochloride
826-39-1

(+/-)-exo-mecamylamine hydrochloride

propargyl bromide
106-96-7

propargyl bromide

N-propargyl mecamylamine

N-propargyl mecamylamine

Conditions
ConditionsYield
With potassium hydrogencarbonate In tetrahydrofuran; N,N-dimethyl-formamide Alkylation; Heating;
(+/-)-exo-mecamylamine hydrochloride
826-39-1

(+/-)-exo-mecamylamine hydrochloride

1-chloromethyl-4-fluorobenzene
352-11-4

1-chloromethyl-4-fluorobenzene

N-(4-fluorobenzyl) mecamylamine

N-(4-fluorobenzyl) mecamylamine

Conditions
ConditionsYield
With potassium hydrogencarbonate In tetrahydrofuran; N,N-dimethyl-formamide Alkylation; Heating;
(+/-)-exo-mecamylamine hydrochloride
826-39-1

(+/-)-exo-mecamylamine hydrochloride

1-bromomethyl-4-nitro-benzene
100-11-8

1-bromomethyl-4-nitro-benzene

N-(4-nitrobenzyl) mecamylamine

N-(4-nitrobenzyl) mecamylamine

Conditions
ConditionsYield
With potassium hydrogencarbonate In tetrahydrofuran; N,N-dimethyl-formamide Alkylation; Heating;
(+/-)-exo-mecamylamine hydrochloride
826-39-1

(+/-)-exo-mecamylamine hydrochloride

S-(+)-mecamylamine hydrochloride

S-(+)-mecamylamine hydrochloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1.) aq. Na2CO3 / 2.) CHCl3, 1 h, room t.
2: 64 percent / ethanol / 0.75 h / Heating
View Scheme

826-39-1Upstream product

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 826-39-1