79 Results for "

rapamycin

" in MedChemExpress (MCE) Product Catalog:
Products (79)

79 Results for "rapamycin" in MCE Product Catalog:

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Cat. No.: HY-122402S
Umirolimus-d5 is the deuterium labeled Umirolimus (HY-122402). Umirolimus, a macrocyclic triene lactone Rapamycin derivative, is powerful immunosuppressant and anti-inflammatory agent. Umirolimus has highly lipophilicity and can be used agent-eluting stent (DES) applications .
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Cat. No.: HY-106979
CAS No.: 186752-78-3
Synonyms: SAR-943
Olcorolimus (SAR-943) is a Rapamycin (HY-10219) derivative. Olcorolimus can reduce IL-4, IL-5, eosinophil, neutrophil, lymphocyte, cellular fibronectin; lung epithelial cell proliferation and mucus hypersecretory phenotype in Ovalbumin (HY-W250978)-sensitized BALB/c mice. Olcorolimus can be used for the researches of inflammation and immunology, such as asthma .
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Cat. No.: HY-10218S1
CAS No.: 1661009-29-5
Synonyms: RAD001-13C2,d4; SDZ-RAD-13C2,d4
Everolimus- 13C2,d4 (RAD001- 13C2,d4) is 13C labeled Everolimus. Everolimus (RAD001) is a Rapamycin (HY-10219) derivative and a potent, selective and orally active mTOR1 inhibitor. Everolimus binds to FKBP-12 to generate an immunosuppressive complex. Everolimus inhibits tumor cells proliferation and induces cell apoptosis and autophagy. Everolimus has potent immunosuppressive and anticancer activities .
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Cat. No.: HY-145931
CAS No.: 1228012-18-7
Purity:  98.41%
Target:  

mTOR Autophagy

Research Areas:  

Cancer

CC214-2 is an oral active and selective mTOR kinase inhibitor. CC214-2 targets to both of mTORC1 (pS6) and mTORC2 (pAktS473). CC214-2 induces autophagy, which is a potential target for host-directed therapy (HDT) in tuberculosis. CC214-2 exhibits synergistic bactericidal and sterilizing activity agasinst tuberculosis (TB), and shortens the treatment duration. CC214-2 also inhibits Rapamycin (HY-10219)-resistant signaling and the growth of glioblastomas in vitro and in vivo .
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Cat. No.: HY-N15267
CAS No.: 64280-22-4
Ovalitenone is a flavonoid compound that can be isolated from the plant Millettia peguensis. It shows no cytotoxic effects on lung cancer H460 and A549 cells, but it significantly inhibits anchorage-independent growth, CSC-like phenotypes, colony formation, and the migration and invasion capabilities of cancer cells. Ovalitenone can significantly reduce the levels of N-cadherin, snail, and slug, while increasing E-cadherin, thus inhibiting the EMT pathway. Additionally, Ovalitenone suppresses the signaling pathways regulated by focal adhesion kinase (FAK), ATP-dependent tyrosine kinase (AKT), mammalian target of rapamycin (mTOR), and cell division cycle 42 (Cdc42) .
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Cat. No.: HY-133770
Target:  

Drug Metabolite

Research Areas:  

Others

Seco Rapamycin ethyl ester is an open-ring metabolite of Rapamycin derivative. Seco-rapamycin is reported not to affect the mTOR function .
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Cat. No.: HY-132003
CAS No.: 1067892-47-0
Target:  

Akt

Research Areas:  

Cancer

Wortmannin-Rapamycin Conjugate 1 (compound 7c) is a furan ring-opened derivative of wortmannin-rapamycin conjugate with potent antitumor activities and a fine water solubility. Wortmannin-Rapamycin Conjugate 1 can inhibit the AKT phosphorylation in the tumor and can be used for cancer research .
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Cat. No.: HY-W765245
Synonyms: Sirolimus-13C,d3-1; AY-22989-13C,d3-1
Rapamycin- 13C,d3-1 (Sirolimus- 13C,d3-1) is the deuterated, 13C-labeled Rapamycin (HY-10219). Rapamycin (Sirolimus; AY 22989) is a potent and specific blood-brain barrier-transmissible mTOR inhibitor with an IC50 of 0.1 nM in HEK293 cells. Rapamycin is a molecular glue that binds FKBP12 and mTOR proteins together, thereby inhibiting mTOR kinase activity. Rapamycin binds to FKBP12 and specifically acts as an allosteric inhibitor of mTORC1. Rapamycin is an autophagy activator, an immunosuppressant .
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Cat. No.: HY-W781875
CAS No.: 150821-39-9
Target:  

mTOR

Research Areas:  

Cancer

Sirolimus isomer C is an impurity of Rapamycin (Sirolimus) (HY-10219) .
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Cat. No.: HY-19555AR
CAS No.: 148554-65-8
Synonyms: Secorapamycin A monosodium (Standard)
Research Areas:  

Others

Phenglutarimid (hydrochloride) (Standard) is the analytical standard of Phenglutarimid (hydrochloride). This product is intended for research and analytical applications. Phenglutarimid hydrochloride is an anticholinergic used as an antiparkinsonian agent.
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Cat. No.: HY-18672
CAS No.: 944153-47-3
Target:  

Autophagy

Research Areas:  

Cancer

SMER18 is a small molecule enhancer of rapamycin which act as a mTOR-independent autophagy inducer.
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Cat. No.: HY-13766
CAS No.: 179033-51-3
Synonyms: VX-853
Target:  

PPAR

Research Areas:  

Others

Timcodar is a macrolide agent, and studies have shown that during adipogenesis, timcodar can significantly inhibit fat accumulation, with an effect similar to that of rapamycin. However, unlike rapamycin, timcodar does not cause immunosuppression and glucose resistance. In addition, timcodar can effectively inhibit the adipogenic transcriptional regulators PPAR?? and C/EBP??, thereby inhibiting genes involved in fat accumulation. These studies lay the foundation for timcodar as a potential anti-obesity therapy, as obesity is becoming a global epidemic.
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Cat. No.: HY-139085A
Purity:  ≥95.0%
Target:  

Drug Intermediate

Research Areas:  

Cancer

XL388-C2-amide-PEG9-NH2 hydrochloride is an intermediate used in the synthesis of C26-linked Rapamycin analog .
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Cat. No.: HY-139085B
Target:  

Drug Intermediate

Research Areas:  

Cancer

XL388-C2-amide-PEG9-NH2 TFA is an intermediate used in the synthesis of C26-linked Rapamycin analog .
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Cat. No.: HY-W339757
CAS No.: 321883-54-9
Research Areas:  

Cancer

Dioctanoylphosphatidic acid sodium functions as a modulator of phagocyte respiratory burst, acts as a precursor to diacylglycerol and lysophosphatidic acid, and influences the phosphorylation of the mammalian target of rapamycin (mTOR) while enhancing the viability of gallbladder carcinoma cells treated with histone deacetylase inhibitors (HDACIs); it is derived from glycerophospholipid through the action of phospholipase D.
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Cat. No.: HY-149861
CAS No.: 2984599-57-5
Target:  

Bacterial

Research Areas:  

Infection

Mip-IN-1(S,S-28i)is a new rapamycin-derived macrophage infectivity potentiator (Mip) inhibitor. Mip-IN-1 displays strong anti-enzymatic activity against the Mip proteins of Neisseria meningitidis and Neisseria gonorrhoeae and substantially improved the ability of macrophages to kill the bacteria .
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Cat. No.: HY-172789
Target:  

mTOR Apoptosis

Research Areas:  

Cancer

mTOR inhibitor-27 (Compound 7e) is a mammalian target of rapamycin (mTOR) inhibitor with an IC50 value of 5.47 μM. mTOR inhibitor-27 can induce tumor cell apoptosis and arrest the cell cycle in the S-phase, thereby inhibiting cancer cell growth. mTOR inhibitor-27 is promising for research of cancers, such as skin cancer .
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Cat. No.: HY-W003943
CAS No.: 903899-13-8
Research Areas:  

Infection

6-Hydroxypyridin-3-ylboronic acid is a heterocyclic building block, which can be used in the synthesis of non-nucleoside inhibitors of hepatitis C virus (HCV) RNA-dependent RNA polymerase nonstructural protein 5B (NS5B). 6-Hydroxypyridin-3-ylboronic acid has also been used in the synthesis of mammalian target of rapamycin (mTOR) inhibitors .
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Cat. No.: HY-116191
CAS No.: 1309087-83-9
Target:  

PI3K mTOR

Research Areas:  

Cancer

WJD008 is a potent dual phosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) inhibitor with antiproliferative and anticlonogenic activity in tumor cells and transformed cells with PIK3CA mutant. WJD008 inhibits kinase activity of PI3K α and mTOR and abrogates insulin-like growth factor-I-activated PI3K-Akt-mTOR signaling cascade. WJD008 is promising for research of cancers .
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Cat. No.: HY-185200
CAS No.: 155589-16-5
Target:  

Drug Derivative

Research Areas:  

Others

Rapamycin 42-hemisuccinate is a Rapamycin (HY-10219) derivative used in the synthesis of sterolated Rapamycin liposomes .
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