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Home > Encyclopedia > Dibazole

Dibazole

pharmaceutical raw materials
Dibazole structure

Dibazole 

structure
  • CAS No:

    621-72-7

  • Formula:

    C14H12N2

  • Chemical Name:

    Dibazole

  • Synonyms:

    1H-Benzimidazole,2-(phenylmethyl)-;Benzimidazole,2-benzyl-;2-(Phenylmethyl)-1H-benzimidazole;Bendazol;2-Benzylbenzimidazole;Dibasol;Dibazol;Dibazole;Tromasedan;Bendazole;NSC 60020;NSC 631632;2-Benzyl-1H-benzimidazole;2-Benzyl-1H-benzo[d]imidazole;2-Benzyl-1H-1,3-benzodiazole;2-Benzyl-1H-benzoimidazole;102389-81-1

  • Categories:

    Active Pharmaceutical Ingredients  >  Circulatory System Drugs

Description

Bendazol is a hypotensive drug which can also enhance NO synthase activity in renal glomeruli and collecting tubules.


Bendazol is a member of benzimidazoles.

Dibazole Basic Attributes

208.26

208.26

210-703-6

26601THN1D

631632|60020

DTXSID80211157

2933990090

Characteristics

28.7

3.2

White or almost white crystalline powder

1.14 g/cm3 @ Temp: 298.15 °C

187 °C

453.5ºC at 760 mmHg

252.1±9.3 °C

1.680

>31.2 [ug/mL]

Oral-Mouse LD50: 100 mg/kg; Abdominal cavity-mouse LD50: 240 mg/kg

Flammable; burning produces toxic nitrogen oxide fumes

Safety Information

IRRITANT

Ventilated, low temperature and dry; stored separately from food materials in warehouse

P261, P264, P270, P271, P280, P301+P310, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501

H301

|Danger|H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P310, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Toxicity

highly toxic

Drug Information

Substances that augment, stimulate, activate, potentiate, or modulate the immune response at either the cellular or humoral level. The classical agents (Freund's adjuvant, BCG, Corynebacterium parvum, et al.) contain bacterial antigens. Some are endogenous (e.g., histamine, interferon, transfer factor, tuftsin, interleukin-1). Their mode of action is either non-specific, resulting in increased immune responsiveness to a wide variety of antigens, or antigen-specific, i.e., affecting a restricted type of immune response to a narrow group of antigens. The therapeutic efficacy of many biological response modifiers is related to their antigen-specific immunoadjuvanticity. (See all compounds classified as Adjuvants, Immunologic.)|Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS. (See all compounds classified as Antihypertensive Agents.)|Agents that promote the production and release of interferons. They include mitogens, lipopolysaccharides, and the synthetic polymers Poly A-U and Poly I-C. Viruses, bacteria, and protozoa have been also known to induce interferons. (See all compounds classified as Interferon Inducers.)|A heterogeneous group of drugs used to produce muscle relaxation, excepting the neuromuscular blocking agents. They have their primary clinical and therapeutic uses in the treatment of muscle spasm and immobility associated with strains, sprains, and injuries of the back and, to a lesser degree, injuries to the neck. They have been used also for the treatment of a variety of clinical conditions that have in common only the presence of skeletal muscle hyperactivity, for example, the muscle spasms that can occur in MULTIPLE SCLEROSIS. (From Smith and Reynard, Textbook of Pharmacology, 1991, p358) (See all compounds classified as Muscle Relaxants, Central.)

2-benzylbenzimidazole

Dibazole Use and Manufacturing

It can relax blood vessels, lower blood pressure, relieve smooth muscle spasm and stimulate the spinal cord. Used for hypertension, angina pectoris, toxemia of pregnancy, gastrointestinal spasm, sequelae of poliomyelitis, peripheral facial paralysis, etc.

Computed Properties

Molecular Weight:208.26
XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:208.100048391
Monoisotopic Mass:208.100048391
Topological Polar Surface Area:28.7
Heavy Atom Count:16
Complexity:223
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Drug Function and Efficacy

Not yet clear

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

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