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Isothipendyl

Isothipendyl structure

Isothipendyl 

structure
  • CAS No:

    482-15-5

  • Formula:

    C16H19N3S

  • Chemical Name:

    Isothipendyl

  • Synonyms:

    10H-Pyrido[3,2-b][1,4]benzothiazine-10-ethanamine,N,N,α-trimethyl-;10H-Pyrido[3,2-b][1,4]benzothiazine,10-[2-(dimethylamino)propyl]-;N,N,α-Trimethyl-10H-pyrido[3,2-b][1,4]benzothiazine-10-ethanamine;D 201;AY 56012;Dimethylaminoisopropylazaphenothiazine;10-[2-(Dimethylamino)propyl]-10H-pyrido[3,2-b][1,4]benzothiazine;10-(2-Dimethylaminopropyl)-9-thia-1,10-diazaanthracene;10-(2-Dimethylaminopropyl)thiophenylpyridylamine;Isothipendyl;10-(2-Dimethylamino-2-methylethyl)-10H-pyrido[3,2-b][1,4]benzothiazine;10-(2-Dimethylaminopropyl)-1-azaphenothiazine;N-Dimethylaminoisopropylthiophenylpyridylamine;Udantol;Odantol;(±)-Isothipendyl

  • Categories:

    Organic Chemistry  >  Heterocyclic Ring

Description

Solid


Solid


Isothipendyl is a tertiary amino compound and an aromatic amine.|Isothipendyl is an antihistamine and anticholinergic used as an antipruritic.

Isothipendyl Basic Attributes

285.409

285.41

207-578-5

DTXSID5048267

D04AA22|D - Dermatologicals|R - Respiratory system

Characteristics

44.7

3.69940

Solid

1.167g/cm3

213-216

172.5 °C

208.6ºC

1.62

2.63E-07mmHg at 25°C

LD50 in mice (mg/kg): 65 ±2 i.p.; 222 ±18 orally (Schlichtegroll)

Safety Information

P264, P270, P301+P312, P330, P501

H302

Drug Information

For the topical treatment of itching associated with allergic reactions.

Isothipendyl, an azaphenothiazine derivative, competitively binds to histamine (H1) receptors, resulting in inhibition of the pharmacological effects of histamines. It also has some sedative, anticholinergic and antiserotoninergic effects.

Drugs that bind to but do not activate histamine receptors, thereby blocking the actions of histamine or histamine agonists. Classical antihistaminics block the histamine H1 receptors only. (See all compounds classified as Histamine Antagonists.)

Isothipendyl is a selective histamine H1 antagonist and binds to the histamine H1 receptor. This blocks the action of endogenous histamine, which subsequently leads to temporary relief of the negative symptoms brought on by histamine.

10-(2-dimethylamino-2-methylethyl)-10H-pyrido(3,2- b)(1,4)benzothiazine

Isothipendyl Use and Manufacturing

Uses

Antihistaminic.

Pharmaceuticals

Computed Properties

Molecular Weight:285.4
XLogP3:3.5
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:285.12996879
Monoisotopic Mass:285.12996879
Topological Polar Surface Area:44.7
Heavy Atom Count:20
Complexity:323
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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    CAS No.: 482-15-5
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