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Rimantadine hydrochloride

pharmaceutical raw materials
Rimantadine hydrochloride structure

Rimantadine hydrochloride 

structure
  • CAS No:

    1501-84-4

  • Formula:

    C12H21N.ClH

  • Chemical Name:

    Rimantadine hydrochloride

  • Synonyms:

    Tricyclo[3.3.1.13,7]decane-1-methanamine,α-methyl-,hydrochloride (1:1);1-Adamantanemethylamine,α-methyl-,hydrochloride;Tricyclo[3.3.1.13,7]decane-1-methanamine,α-methyl-,hydrochloride;EXP 126;α-Methyl-1-adamantanemethylamine hydrochloride;Rimantadine hydrochloride;1-(1-Aminoethyl)adamantane hydrochloride;Remantadine;Meradan;Meradane;JP 61;Remantadin;Flumadine;Roflual;NSC 206764;1-(1-Adamantyl)ethylamine hydrochloride;1-(Adamantan-1-yl)ethan-1-amine hydrochloride;12710-47-3;33122-80-4

  • Categories:

    Active Pharmaceutical Ingredients  >  Synthetic Anti-infective Drugs

Description

White Crystalline SolidRimantadine hydrochloride is an antiviral analogue of amantadine, reportedly useful in the prophylaxis and treatment of influenza A. Compared with amantadine, nmantadine appears to have a lower side-effect profile.


Rimantadine hydrochloride is an organic molecular entity.|An RNA synthesis inhibitor that is used as an antiviral agent in the prophylaxis and treatment of influenza.

Rimantadine hydrochloride Basic Attributes

215.76

215.144073

1806241-263-5

759149|206764

DTXSID1047813

29213000

Characteristics

26

4.05230

white crystalline solid

373-375 °C

247.8ºC at 760mmHg

99.3ºC

Freely soluble in water.

-20°C Freezer

0.0251mmHg at 25°C

Oral-rat LD50: 640 mg/kg;Abdominal cavity-mouse LD50: 135 mg/kg

Flammable; burning produces toxic nitrogen oxides and hydrogen chloride fumes

146.2 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]

Safety Information

NONH for all modes of transport

3

22-36/37/38

26-36

AU4717000

Xn

Warehouse ventilated, low temperature and dry

P261-P305 + P351 + P338

H302-H315-H319-H335

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, 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 44 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Toxicity

moderately toxic

Drug Information

Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly. (See all compounds classified as Antiviral Agents.)|Compounds that inhibit cell production of DNA or RNA. (See all compounds classified as Nucleic Acid Synthesis Inhibitors.)

Flumadine

Rimantadine hydrochloride Use and Manufacturing

Uses

Used as an antiviral agent

Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients

Computed Properties

Molecular Weight:215.76
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:215.1440774
Monoisotopic Mass:215.1440774
Topological Polar Surface Area:26
Heavy Atom Count:14
Complexity:180
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

Drug Function and Efficacy

This product is an antiviral drug, mainly active against influenza A virus. It inhibits the proliferation of type A viruses in vitro, including H1N1, H2N2 and H3N2 subtypes isolated from humans. It has both preventive and therapeutic effects on animals infected with influenza A myxovirus. It may work early in the viral replication cycle by inhibiting the uncoating of viral particles in host cells. It does not suppress the immune response after exposure to influenza A virus. It has only a weak effect on other types of influenza viruses.

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

Registered Holders

  • Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.

    China China
    Active
  • NORTHEAST Pharmaceutical Group Co., Ltd.

    China China
    Active
  • Olpha AS

    United States United States
    Active

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