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CAS:10361-46-3
Molecular Formula:Bi5H9N4O22
Alias
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Bismuth Subnitrate; Bismuth Nitrate Oxide; Oxobismuthanyl Nitrate
Brief Introduction
It is used to test sugars and alkaloids in clinical tests. Manufacturing bismuth salt and ceramic glaze. Medically, it is a medicine for neutralizing gastric acid and astringent. It is used for gastric and duodenal ulcer and diarrhea
CAS:104987-11-3
Molecular Formula:C44H69NO12
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Fujimycin; Prograf; Protopic; Fk506; Tacrolimus Anhydrous; Advagraf; Modigraf; Protopy; Anhydrous Tacrolimus; 8-Deethyl-8-[But-3-Enyl]-Ascomycin; Unii-Y5L2157C4J; (-)-Fk 506; Tsukubaenolide; Prograf (Tn); Prograft; Avagraf; Envarsus; Graceptor; Envarsus Xr; (3S,4R,5S,8R,9E,12S,14S,15R,16S,18R,19R,26As)-5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26A-Hexadecahydro-5,19-Dihydroxy-3-[(1E)-2-[(1R,3R,4R)-4-Hydroxy-3-Methoxycyclohexyl]-1-Methylethenyl]-14,16-Dimethoxy-4,10,12,18-Tetramethyl-8-(2-Propen-1-Yl)-15,19-Epoxy-3H-Pyrido[2,1-C][1,4]Oxaazacyclotricosine-1,7,20,21(4H,23H)Tetrone
Brief Introduction
Tacrolimus is a macrolide drug isolated from Streptomyces, which has strong immunosuppressive effect. Tacrolimus can specifically bind and inhibit calmodulin phosphatase activity, inhibit IL-2 signal transcription, thus inhibit T cell activation and TNF- α、 IL-1 β And IL-6 production and T cell dependent B cell proliferation. Compared with cyclosporine, another calmodulin phosphatase inhibitor, tacrolimus has stronger inhibitory effect on T cell activation and less adverse reactions.
CAS:106941-25-7
Molecular Formula:C8H12N5O4P
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((2-(6-Amino-9H-Purin-9-Yl)Ethoxy)Methyl)Phosphonic Acid; Pmea; Treatment Adefovir; Tenofovir Desmethyl Impurity; 2-(6-Amino-9H-Purin-; Adefovir Dipivox (Pmea); [[2-(6-Amino-9H-Purin-9-Yl)Ethoxy]; Methyl]Phosponic Acid; P-[[2-(6-Amino-9H-Purin-9-Yl)Ethoxy]Methyl]Phosphonic Acid; Adefovir(Pmea)
Brief Introduction
Adefovir is a acyclic nucleoside analogue of adenosine monophosphate. It is a new type of anti HBV drug. It is used in the form of the former drug A Duff Vee ester, and belongs to adenine nucleoside. Under the action of cell kinase, Adefovir is phosphorylated to an active metabolite, namely adefovir diphosphate. Adefovir diphosphate inhibits HBV DNA polymerase (reverse transcriptase) in two ways. One is that it competes with the natural substrate deoxyadenosine triphosphate, and the other is that it causes DNA strand elongation and termination after integration into virus DNA. Therefore, Adefovir is mainly used for the treatment of adult chronic hepatitis B patients with evidence of active replication of hepatitis B virus, continuous increase of serum amino acid transferase (ATL or AST), or liver tissue active lesions with liver function compensation.
CAS:107648-80-6
Molecular Formula:C19H26Cl2N6O5S2
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Pyrrolidinium,1-[[(6R,7R)-7-[[(2Z)-2-(2-Amino-4-Thiazolyl)-2-(Methoxyimino)Acetyl]Amino]-2-Carboxy-8-Oxo-5-Thia-1-Azabicyclo[4.2.0]Oct-2-En-3-Yl]Methyl]-1-Methyl-,Chloride,Hydrochloride (1:1:1; 1-[[(6R,7R)-7-[2-(2-Amino-4-Thiazolyl)-2-(Z-Methoxyimino)-Acetamido]-2-Carboxy-8-Oxo-5-Thia-1-Azabicyclo[4.2.0]Oct-2-En-3-Yl]Methyl]-1-Methyl-Pyrrolidinium Chloride,Monohydrochloride; L-[[(6R,7R)-7-[2-(2-Amino-4-Thiazolyl)-Glyoxylamido]-2-Carboxy-8-Oxo-5-Thia-L-Azabicyclo[4.2.0]Oct-2-En-3-Yl]Methyl]-1-Methyl-Pyrrolidinium Chloride; 1-[[(6R,7R)-7-[[(2Z)-(2-Amino-4-Thiazolyl)(Methoxyimino)Acetyl]Amino]-2-Carboxy-8-Oxo-5-Thia-1-Azabicyclo[4.2.0]Oct-2-En-3-Yl]Methyl]-1-Methyl-Pyrrolidinium Chloride Hydrochloride; Cefepime Dihydrochloride; (6R,7R)-7-[[(2E)-2-(2-Amino-1,3-Thiazol-4-Yl)-2-Methoxyiminoacetyl]Amino]-3-[(1-Methylpyrrolidin-1-Ium-1-Yl)Methyl]-8-Oxo-5-Thia-1-Azabicyclo[4.2.0]Oct-2-Ene-2-Carboxylic Acid Chloride Hydrochloride; Cefepime Hcl Sterile Powder; Cefepime Hcl; Cefepime Hydrochloric; Pyrrolidinium,1-[[(6R,7R)-7-[[(2Z)-2-(2-Amino-4-Thiazolyl)-2-(Me
Brief Introduction
For the treatment of a variety of bacterial infections, including severe infections.
CAS:108612-45-9
Molecular Formula:C24H25FN6O
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Mizolastine; Mizollen; Zolistan; Sl 85.0324
Brief Introduction
Mizolastine is an antihistamine, also known as mizolastine. It not only has strong antihistamine effect, but also can inhibit other inflammatory transmitters, such as inhibiting the production of leukotrienes and reducing edema. Therefore, in theory, mizolastine not only has antihistamine and antiallergic effects, but also has anti-inflammatory activity. It is the preferred drug for the treatment of acute urticaria. It takes effect significantly faster than other antihistamines. After 1 ~ 3 hours, the number of wind masses is reduced, the degree of pruritus is reduced, and the maintenance time is long, up to 24 hours. At present, it is mainly used to treat skin allergy symptoms such as urticaria, seasonal allergic rhinitis (hay fever) and perennial allergic rhinitis in adults or children over 12 years old.
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