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Search results for benzyl root_references_citation in Reference Text / Citation (approximate match)
Status:
Possibly Marketed Outside US
First approved in 2011
Source:
21 CFR 352
Source URL:
Class (Stereo):
CHEMICAL (RACEMIC)
Conditions:
The drug stimulates erythrocytes and leucopoiesis. Applied for the prevention of radiation sickness with X-ray and radiotherapy. For a better intake to take batilol together with a small amount of vegetable oil or butter. Side-effects are neuralgia and allergic reactions.
Status:
Possibly Marketed Outside US
Source:
21 CFR 333C
(2014)
Source URL:
First approved in 2011
Source:
M016
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Benzyl acetate is used as a fragrance ingredient and occurs in different plants and fruits, e.g., jasmine, apple, tea, plum, wine grape. It possesses a sweet and pleasant aroma, owing to which, it finds applications in personal hygiene and health care products.
Status:
Possibly Marketed Outside US
Source:
SALIGENIN by Leroux, H. at Vitry le François
Source URL:
First approved in 2011
Source:
21 CFR 333D
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
Salicyl alcohol is used as a local anesthetic and antiinflammatory. A light brown crystalline powder, stable, incompatible with acids, acid chlorides, acid anhydrides, strong oxidizing agents. It was found in bark of willow tree family and aspen Populus tremula. It is a well-known allergen in phenol-formaldehyde resins found to cause allergic contact dermatitis. Antioxidant activity of 2-hydroxybenzyl alcohol has been reported.
Status:
Possibly Marketed Outside US
Source:
21 CFR 358H
(2009)
Source URL:
First approved in 2009
Source:
21 CFR 358H
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Status:
Possibly Marketed Outside US
Source:
NCT03394950: Phase 4 Interventional Completed Stroke, Ischemic
(2018)
Source URL:
First approved in 2009
Source:
21 CFR 352
Source URL:
Class (Stereo):
CHEMICAL (RACEMIC)
3-N-Butylphthalide (NBP), a family comprised of optical isomers l-3-N-butylphthalide (l-NBP) and d-3-N-butylphthalide (d-NBP), with l-NBP being an extract from seeds of Apium graveolens Linn. (celery) and dl-3-N-butylphthalide (dl-NBP), a synthetized version, has been studied for its significant neuroprotective effects. NBP showed neuroprotective effects by decreasing oxidative damage, inhibiting inflammatory responses, improving mitochondrial function, and reducing
neuronal apoptosis. NBP received approval by the State Food and Drug Administration of China for clinical use in stroke patients in 2002. It demonstrates a potential for the treatment of central nervous system diseases, including Parkinson’s disease, Alzheimer’s disease.
Status:
Possibly Marketed Outside US
Source:
ANDA072781
(2009)
Source URL:
First approved in 2009
Source:
ANDA072781
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Sodium isobutoxide is an alkoxide of isobutanol. It is used in organic chemistry for the synthesis of isobutyl ethers.
Status:
Possibly Marketed Outside US
First approved in 2006
Source:
21 CFR 347
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
Benzyl cinnamate (also known as Jacobson's solution) was used to treat chronic salpingitis, and in combination with vitamin A to treat cerebrovascular lesions. In addition, it is used in heavy oriental perfumes and as a fixative and as a flavoring agent.
Status:
Possibly Marketed Outside US
Source:
NCT00515151: Phase 4 Interventional Completed Catheterization, Central Venous
(2002)
Source URL:
First approved in 2006
Source:
21 CFR 333E
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Propyl alcohol or n-Propanol, primary alcohol that is used as a solvent and chemical intermediate in the pharmaceutical, chemical and food industries. It was found that n-Propanol exhibited low acute toxicity for animals via the dermal, inhalation, and oral routes of exposure. n-Propanol has no evidence of carcinogenicity or mutagenicity. This compound is not a reproductive toxicant at levels expected from using it as an inert ingredient in pesticide formulations.
Status:
Possibly Marketed Outside US
Source:
LIDOTHOL by Preferred Pharmaceuticals Inc.
(2018)
Source URL:
First approved in 2005
Source:
M006
Source URL:
Class (Stereo):
CHEMICAL (RACEMIC)
Status:
Possibly Marketed Outside US
Source:
M006
(2004)
Source URL:
First approved in 2004
Source:
M006
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)