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CAS:207233-91-8
Molecular Formula:C3H9NaO4S3
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2,3-Dichloro-5-Hydroxypyridine; 2,3-Dimercaptopropanesulfonic Acid Sodium Salt Monohydrate,Dmps; Sodium Dl-2,3-Dithiopropanesulphonate Monohydrate; 2,3-Dimercaptopropanesulfonic Acid Sodium Salt Monohydrate Dmps; Sodium 2,3-Dimercaptopropanesulfonate Monohydrate; 2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate; Dl-2,3-Dimercapto-1-Propanesulfonic Acid,Sodium Salt Monohydrate; Mfcd00149543
Brief Introduction
Rubber and pharmaceutical industries. Antidote for heavy metal poisoning.
CAS:208110-64-9
Molecular Formula:C20H22ClF2N3O
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Unii-Rat9Oha1Yh; Befiradol; Nlx-112; Rat9Oha1Yh
Brief Introduction
Befiradol (F-13,640; NLX-112) is a very potent and highly selective 5-HT1A receptor full agonist. It has powerful analgesic and antiallodynic effects comparable to those of high doses of opioid painkillers, but with fewer and less prominent side effects, as well as little or no development of tolerance with repeated use. A SAR study revealed that replacement of the dihalophenyl moiety by 3-benzothienyl increases maximal efficacy from 84% to 124% (Ki=2.7 nM).
Befiradol was discovered and developed by Pierre Fabre Médicament, a French pharmaceuticals company. In September 2013, befiradol was out-licensed to Neurolixis, a California-based biotechnology company. Neurolixis announced that it intends to re-purpose befiradol for the treatment of Levodopa-induced dyskinesia in Parkinson's disease. In support of this indication, preclinical data was published describing the activity of befiradol in animal models of Parkinson's disease.
CAS:20830-81-3
Molecular Formula:C27H29NO10
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(8S-Cis)-8-Acetyl-10-((3-Amino-2,3,6-Trideoxy-Alpha-L-Lyxo-Hexopyranosyl)Oxy)-7,8,9,10-Tetrahydro-6,8,11-Trihydroxy-1-Methoxy-5,12-Naphthacenedione Hydrochloride; Daunorubicine Hydrochloride; Daunomycin Hydrochloride; Leukaemomycin C Hydrochloride; (8S-Cis)-8-Acetyl-10-[(3-Amino-2,3,6-Trideoxy-Alpha-L-Lyxo-Hexopyrannosyl)Oxy]; 3-Acetyl-1,2,3,4,6,11-Hexahydro-3,5,12-Trihydroxy-10-Methoxy-6,11-Dioxo-1-Naph
Brief Introduction
Daunorubicin is an anthracycline antibiotic that has antineoplastic activity and is used in the therapy of acute leukemia and AIDS related Kaposi sarcoma. Daunorubicin is associated with a low rate of transient serum enzyme and bilirubin elevations during therapy, but has not been implicated in cases of clinically apparent acute liver injury with jaundice.
CAS:208538-73-2
Molecular Formula:C56H70N9NaO23S
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Pneumocandin A0, 1-[(4R,5R)-4,5-Dihydroxy-N2-[4-[5-[4-(Pentyloxy)Phenyl]-3-Isoxazolyl]Benzoyl]-L-Ornithine]-4-[(4S)-4-Hydroxy-4-[4-Hydroxy-3-(Sulfooxy)Phenyl]-L-Threonine]-, Sodium Salt (1:1); 1-[(4R,5R)-4,5-Dihydroxy-N2-[4-[5-[4-(Pentyloxy)Phenyl]-3-Isoxazolyl]Benzoyl]-L-Ornithine]-4-[(4S)-4-Hydroxy-4-[4-Hydroxy-3-(Sulfooxy)Phenyl]-L-Threonine]Pneumocandin A0 Monosodium Salt; Funguard; Micafungin Sodium(Fk-463, Mycamine); Mycamine; Cs-705; Fk 463; Funguard; Mycamine; Micafungin Sodium Impurity
Brief Introduction
Micafungin sodium is the second echinocandin drug used in clinic after caspofungin. It is an antifungal drug developed by Estelle company of Japan. It was first listed in Japan in 2002 and approved by FDA in the United States in May 2005. Its indications are mycosis caused by Aspergillus and Candida, respiratory mycosis and gastrointestinal mycosis. In addition, amphotericin and triazole antifungal drugs were used in combination.
CAS:2098-66-0
Molecular Formula:C22H27ClO3
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Ciproterona; Ciproterone; Cyproteronum; (1S,2S,3S,5R,11R,12S,15R,16S)-15-Acetyl-9-Chloro-15-Hydroxy-2,16-Dimethylpentacyclo[9.7.0.02,8.03,5.012,16]Octadeca-7,9-Dien-6-One
Brief Introduction
The inhibitory effect of cyproterone on anterior pituitary gonadotropin is stronger than progesterone, and has strong anti androgen and anti progesterone effects. It is clinically used for central early puberty (inhibiting premature bone maturation and excessive growth) and for the treatment of advanced prostate cancer.
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