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99% Tacrolimus Tacrolimus Manufacturer Macrolide Antibiotics
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Tacrolimus Basic information |
Product Name: | Tacrolimus |
Synonyms: | (2-propenyl)-,(3s-(3r*(e(1s*,3s*,4s*)),4s*,5r*,8s*,9e,12r*,14r*,15s*,16r*,18s*;,19s*,26ar*))-;16-dimethoxy-4,10,12,18-tetramethyl-8-3-(2-(4-hydroxy-3-methoxycyclohexyl)-1;19-epoxy-3h-pyrido(2,1-c)(1,4)oxaazacyclotricosine-1,7,20,21(4h,23h)-tetrone,5,6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-hexadecahydro-5,19-dihydroxy-3-(2-(4-hydroxy-3-methoxycyclohexyl)-14,16-dim;6,8,11,12,13,14,15,16,17,18,19,24,25,26,26a-hexadecahydro-5,19-dihydroxy-5;fr900506;prograf;tsukubaenolide |
CAS: | 104987-11-3 |
MF: | C44H69NO12 |
MW: | 804.02 |
EINECS: | 1308068-626-2 |
Product Categories: | Active Pharmaceutical Ingredients;Immunosuppressant.;Intermediates & Fine Chemicals;Pharmaceuticals;API;Chiral Reagents;Fujimycin, Prograf;antibiotic;Inhibitors |
Mol File: | 104987-11-3.mol |
Tacrolimus Chemical Properties |
Melting point | 113-115°C |
Fp | 2℃ |
storage temp. | −20°C |
solubility | DMSO: >3 mg/mL |
form | solid |
color | white |
Water Solubility | Freely soluble in DMSO or ethanol. Poorly soluble in water.Soluble in dimethyl sulfoxide, ethanol, water, acetone, chloroform, ethyl acetate, ether, methanol and dimethyl formamide. |
CAS DataBase Reference | 104987-11-3(CAS DataBase Reference) |
Safety Information |
Hazard Codes | T,Xi,Xn,F |
Risk Statements | 25-36/37/38-36-20/21/22-11 |
Safety Statements | 45-36-26-36/37-16-60-20 |
RIDADR | UN 2811 6.1/PG 3 |
WGK Germany | 3 |
RTECS | KD4201200 |
HazardClass | 6.1 |
Tacrolimus Usage And Synthesis |
Chemical Properties | White Crystalline Solid |
Uses | An immunosuppressant that blocks T cell proliferation in vitro by inhibiting the generation of several lymphokines, especially IL-2. Shown to inhibit the activity of FK-506 binding protein, thereby reversing its effects on sarcoplasmic reticulum Ca+2 release. |
Uses | FK-506 (Tacrolimus) is a macrolide immunosuppressive drug that is mainly used after allogeneic organ transplant to reduce the activity of the patient's immune system |
Uses | Tacrolimus (fujimycin) was discovered as a potent inhibitor of IL2 production in a targeted search for novel immunosuppressants. Tacrolimus acts by blocking T cell proliferation in vitro by inhibiting the generation of several lymphokines, notably the original target IL-2. Tacrolimus inhibits the activity of FK-506 binding protein, Ca2+-dependent phosphatase and calcineurin, and activates NF-κB through phosphorylation and degradation of IκBα. |
Uses | treatment of Cushing's syndrome |
Uses | For use after allogenic organ transplant to reduce the activity of the patient's immune system and so the risk of organ rejection. It was first approved by the FDA in 1994 for use in liver transplantation, this has been extended to include kidney, heart, |
Definition | ChEBI: Tacrolimus is a macrolide containing a 23-membered lactone ring, originally isolated from the fermentation broth of a Japanese soil sample that contained the bacteria Streptomyces tsukubaensis. |
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