AAG IMMUNOMYCIN 4-hydroxy-3-methoxycyclohexyl
1.Certificate Of Analysis (COA)
2.Material Safety Data Sheet (MSDS)
3.Route of synthesis (ROS)
4.Method of Aanlysis(MOA)
5.Nuclear Magnetic Resonance(NMR)
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Product Name: | Ascomycin |
Synonyms: | AAG;FK-520;FR-900520;IMMUNOMYCIN;ASCOMYCIN, STREPTOMYCES HYGROSCOPICUS;ASCOMYCIN, STREPTOMYCES HYGROSCOPICUS VAR ASCOMYCETICUS;12,18-tetramethyl-,(3s-(3r*(e(1s*,3s*,4s*)),4s*,19s*,26ar*))--10;8-ethyl-3-(2-(4-hydroxy-3-methoxycyclohexyl)-1-methylethenyl)-14,16-dimethoxy |
CAS: | 104987-12-4 |
MF: | C43H69NO12 |
MW: | 792.01 |
EINECS: | 200-835-2 |
Product Categories: | Intermediates & Fine Chemicals;Pharmaceuticals;Macrolactams;Antibiotics;Antibiotics A to;Antibiotics A-FAntibiotics;Antibiotics by Application;AntifungalAntibiotics;Antineoplastic and Immunosuppressive AntibioticsAntibiotics;Chemical Structure Class;Inhibits an EnzymeAntibiotics;Mechanism of Action;Spectrum of Activity;antibiotic;Inhibitors |
Mol File: | 104987-12-4.mol |
Ascomycin Chemical Properties |
mp | 153-157°C |
storage temp. | −20°C |
Safety Information |
Hazard Codes | Xn,F |
Risk Statements | 20/21/22-36-11 |
Safety Statements | 36/37-16 |
WGK Germany | 3 |
RTECS | KD4185000 |
F | 10 |
Ascomycin Usage And Synthesis |
Chemical Properties | White Solid |
Usage | A potent immunosuppressive agent and could be used as a potential therapeutic agent for autoimmune diseases |
Usage | Ascomycin is a macrocyclic lactone closely related to tacrolimus and rapamycin. Ascomycin is isolated from several species of Streptomyces and was first reported in 1988. Ascomycin exhibits limited, potent antifungal activity but has found considerable utility as an immunosuppressant. |
Usage | Ascomycin is a macrocyclic lactone closely related to tacrolimus and rapamycin. Ascomycin is isolated from several species of Streptomyces and was first reported in 1962. Ascomycin exhibits limited, potent antifungal activity but has found considerable utility as an immunosuppressant. |
Usage | Everolimus is a semi-synthetic macrocyclic lactone prepared from rapamycin by selective alkylation of the 42-hydroxy group with a silyl-protected hydroxyethyl triflate moiety, followed by addition of an ethylhydroxy moiety to provide greater stability and bioavailability. Like all tacrolimus analogues, everolimus binds to receptor protein, FKBP12. The complex then binds to mTOR preventing it from interacting with target proteins. Everolimus is extensively cited in the literature with over 2,000 citations. |
Ascomycin Preparation Products And Raw materials |
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