Oxacyclohexane Open Ring Tacrolimus

Product Name Oxacyclohexane Open Ring Tacrolimus
Alternate Names Tacrolimus Impurities, Impurities of Tacrolimus
CAT No. CS-ED-00227
CAS No. 144432-23-5
Category Impurities
Stock IN-Stock
Mol. Wt. 822.03 g/mol
Mol. For. C₄₄H₇₁NO₁₃
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Tacrolimus
Therapeutic Immunosuppressants
Smileys O=C(O[C@@H]([C@@H]([C@H](CC([C@@H](/C=C(C[C@H](C)C1)/C)CC=C)=O)O)C)/C(C)=C/[C@H](CC[C@H]2O)C[C@H]2OC)[C@@](CCCC3)([H])N3C(C(O)(C([C@@H](C[C@]([C@@H]([C@@]1([H])OC)O)([H])OC)C)=O)O)=O
Controlled No
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Oxacyclohexane open ring Tacrolimus is a chemical compound used in the treatment of organ transplant rejection and autoimmune diseases. It is a potent immunosuppressive drug that helps to prevent the body from rejecting transplanted organs by inhibiting the activity of T lymphocytes. Tacrolimus works by binding to a protein called FKBP-12, which then binds to and inhibits a protein called calcineurin. Calcineurin is involved in the activation of T lymphocytes, which play a key role in the immune response. By inhibiting calcineurin, Tacrolimus prevents the activation of T lymphocytes and reduces the risk of rejection. Oxacyclohexane open ring Tacrolimus is typically administered orally or through injection. The drug is metabolized by the liver and excreted through the kidneys. It has a half-life of approximately 12 hours and reaches peak concentration in the blood within 1-2 hours of administration. The chemical formula of Oxacyclohexane open ring Tacrolimus is C44H69NO12. It is a macrolide lactone compound that belongs to the class of drugs known as calcineurin inhibitors. The molecular weight of Tacrolimus is 804.02 g/mol. It is a white to off-white crystalline powder that is highly soluble in water and ethanol. In conclusion, Oxacyclohexane open ring Tacrolimus is a potent immunosuppressive drug that is used to prevent organ transplant rejection and treat autoimmune diseases. Its chemical structure and mechanism of action make it an effective and valuable medication in the field of transplant medicine.

Related Compounds

Tacrolimus Impurity III | Tacrolimus Dehydro Impurity | Tacrolimus Regioisomer | Tacrolimus Impurity 18 | Tacrolimus impurity-1 | Tacrolimus Impurity 21 | Tacrolimus Ring-opening Impurity | Tacrolimus Butenyl analogue | Tacrolimus C4-epimer Diene | Tacrolimus Impurity 6 (Tacrolimus Hydroxy Acid Impurity) | Tacrolimus alpha-Hydroxy Acid (TAC-H1) | Tacrolimus EP Impurity B | Tacrolimus 21-carboxylic acid | Tacrolimus Impurity 23 | Tacrolimus EP Impurity H | Tacrolimus Impurity I | Tacrolimus Diene | Tacrolimus Impurity 39 | Tacrolimus Impurity VII | Tacrolimus EP Impurity F | Tacrolimus Methyl Acryl Aldehyde | Tacrolimus Lactone Isomer | Tacrolimus impurity | Tacrolimus Impurity X | Tacrolimus Related Compound A | Tacrolimus 8-Propyl Analog |

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