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Tacrolimus monohydrate
[CAS# 109581-93-3]

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Complete supplier list of Tacrolimus monohydrate
Identification
Classification Biochemical >> Inhibitor >> Immune inhibitor
Name Tacrolimus monohydrate
Synonyms (1R,9S,12S,13R,14S,17R,18E,21S,23S,24R,25S,27R)-1,14-dihydroxy-12-[(E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-23,25-dimethoxy-13,19,21,27-tetramethyl-17-prop-2-enyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9]octacos-18-ene-2,3,10,16-tetrone;hydrate
Molecular Structure CAS # 109581-93-3, Tacrolimus monohydrate, (1R,9S,12S,13R,14S,17R,18E,21S,23S,24R,25S,27R)-1,14-dihydroxy-12-[(E)-1-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]prop-1-en-2-yl]-23,25-dimethoxy-13,19,21,27-tetramethyl-17-prop-2-enyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9]octacos-18-ene-2,3,10,16-tetrone,hydrate
Molecular Formula C44H69NO12.H2O
Molecular Weight 822.03
CAS Registry Number 109581-93-3
EC Number 634-559-2
SMILES C[C@@H]1C[C@@H]([C@@H]2[C@H](C[C@H]([C@@](O2)(C(=O)C(=O)N3CCCC[C@H]3C(=O)O[C@@H]([C@@H]([C@H](CC(=O)[C@@H](/C=C(/C1)\C)CC=C)O)C)/C(=C/[C@@H]4CC[C@H]([C@@H](C4)OC)O)/C)O)C)OC)OC.O
Safety Data
Hazard Symbols symbol   GHS06 Danger    Details
Hazard Statements H301    Details
Precautionary Statements P264-P270-P301+P316-P321-P330-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.3H301
Specific target organ toxicity - repeated exposureSTOT RE1H372
Reproductive toxicityRepr.2H361
Acute toxicityAcute Tox.3H311
Acute toxicityAcute Tox.3H331
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
CarcinogenicityCarc.2H351
Reproductive toxicityRepr.1BH360FD
Skin irritationSkin Irrit.2H315
Transport Information UN 2811
SDS Available
up Discovory and Applicatios
Tacrolimus, also known as FK506, was discovered in the 1980s by researchers at Fujisawa Pharmaceutical Co., Ltd. The discovery was serendipitous, as it was initially identified as a metabolite produced by the bacterium Streptomyces tsukubaensis during a search for novel immunosuppressive agents. Tacrolimus exhibited potent immunosuppressive properties, particularly in inhibiting T-cell activation, making it a promising candidate for the prevention of organ rejection in transplantation.

Tacrolimus monohydrate revolutionized organ transplantation by significantly improving graft survival rates. As a calcineurin inhibitor, tacrolimus inhibits T-cell activation by binding to the protein FKBP-12, thereby disrupting the signaling pathway required for T-cell activation. It is widely used in solid organ transplantation, particularly in kidney and liver transplants, to prevent acute rejection episodes and improve long-term graft survival. Tacrolimus-based immunosuppressive regimens have become standard of care in transplantation medicine. Tacrolimus has found applications beyond transplantation in the treatment of various autoimmune diseases. It is used off-label in conditions such as rheumatoid arthritis, psoriasis, and inflammatory bowel disease, where aberrant immune responses play a central role in disease pathogenesis. Tacrolimus suppresses the immune system's inflammatory response, providing symptomatic relief and improving disease outcomes in patients with autoimmune disorders. Topical formulations of tacrolimus are used in the treatment of certain dermatologic conditions, such as atopic dermatitis and psoriasis. Tacrolimus ointment acts as an immunomodulator, reducing inflammation and pruritus associated with these conditions. Its use is particularly beneficial in sensitive areas of the skin or when prolonged use of corticosteroids is not desirable. Tacrolimus is also used in the prevention and treatment of graft-versus-host disease (GVHD), a common complication of allogeneic hematopoietic stem cell transplantation. By suppressing the immune response of donor-derived T cells against recipient tissues, tacrolimus helps mitigate the risk of acute and chronic GVHD, improving outcomes in patients undergoing stem cell transplantation.
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