99 Results for "

Ra Inhibitors

" in MedChemExpress (MCE) Product Catalog:
Products (99)

99 Results for "Ra Inhibitors" in MCE Product Catalog:

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Cat. No.: HY-N10076
CAS No.: 1191255-15-8
Ganomycin I is a non-competitive dual inhibitor of α-glucosidase and HMG-CoA reductase, with IC50 values of 0.3 μM and 12.3 μM, respectively. Ganomycin I inhibits HIV-1 protease, with an IC50 of 7.5 μg/mL. Ganomycin I also suppresses RANKL-induced osteoclast differentiation and bone resorption by inhibiting the activation of ERK, JNK and p38 MAPK, as well as downregulating the c-Fos/NFATc1 signaling pathway. Ganomycin I exhibits antibacterial activity against Gram-positive bacteria, and shows weak activity against Mycobacterium tuberculosis H37Ra. It can be used in research related to metabolic diseases, bone metabolism and anti-infection .
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Cat. No.: HY-137007
CAS No.: 1496553-39-9
Target:  

Interleukin Related

Research Areas:  

Others Inflammation/Immunology

SMA-12b is a small molecule analogue of the parasitic worm compound ES-62. SMA-12b has immunomodulatory activity, acting by regulating the expression of multiple inflammatory response genes, especially those associated with inflammatory bodies. SMA-12b significantly reduces the expression of cytokine IL-1β associated with inflammatory bodies and inhibites the production of IL-1β through a mechanism mediated by NRF2. SMA-12b can be used in the study of rheumatoid arthritis (RA) and other autoimmune diseases .
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Cat. No.: HY-106857A
CAS No.: 123060-44-6
Synonyms: HOE 065
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

RA-octil is a derivative related to angiotensin-converting enzyme inhibitors. RA-octil exhibits a memory promoting effect. RA-octil can be used for research on neurological conditions .
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Cat. No.: HY-118689
CAS No.: 1867107-62-7
RA-2 is a negative-gating modulator of KCa2/3 channels with an IC50 of 17 nM. RA-2 inhibits bradykinin-induced endothelium-derived hyperpolarization (EDH)-type relaxation in U46619-precontracted rings. RA-2 can help to define the physiologic and pathomechanistic roles of KCa2/3 in the vasculature, central nervous system, and during inflammation .
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Cat. No.: HY-161762A
CAS No.: 2305572-22-7
Synonyms: (E/Z)-Ra-2034
Target:  

Influenza Virus CHIKV

Research Areas:  

Cancer

(E/Z)-RA-0002034 is a Chikungunya virus (CHIKV) nsP2 protease inhibitor with IC50 of 58 nM. RA-0002034 covalently modifies the catalytic cysteine in a site-specific manner.
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Cat. No.: HY-107644
CAS No.: 123548-16-3
Target:  

mAChR

Research Areas:  

Cardiovascular Disease

AQ-RA 741 is a potent and selective M 2 antagonist. AQ-RA 741 inhibits the vagally or agonist-induced bradycardia in rats, cats and guinea-pigs. AQ-RA 741 is used in bradycardiac disorders research .
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Cat. No.: HY-154962
CAS No.: 2750555-36-1
Target:  

Bcl-2 Family

Research Areas:  

Cancer

Mcl-1 inhibitor 15 (Compound (Ra)-15) is a Mcl-1 inhibitor (Ki: 0.02 nM). Mcl-1 inhibitor 15 can be used for research of cancer .
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Cat. No.: HY-154961
CAS No.: 2750555-21-4
Target:  

Bcl-2 Family

Research Areas:  

Cancer

Mcl-1 inhibitor 14 (Compound (Ra)-10) is an inhibitor of myeloid cell leukemia-1 (MCL-1) with an Ki of 0.018 nM and can be used for anticancer research .
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Cat. No.: HY-106019CR
CAS No.: 1883548-96-6
Synonyms: R75251 dihydrochloride (Standard)
Liarozole (dihydrochloride) (Standard) is the analytical standard of Liarozole (dihydrochloride). This product is intended for research and analytical applications. Liarozole (R75251) dihydrochloride is an imidazole derivative and orally active retinoic acid (RA) metabolism-blocking agent (RAMBA). Liarozole dihydrochloride inhibits the cytochrome P450 (CYP26)-dependent 4-hydroxylation of RA (IC50=7 μM), resulting in increased tissue levels of RA. Liarozole dihydrochloride shows antitumoral properties .
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Cat. No.: HY-163750
Target:  

COX

Research Areas:  

Inflammation/Immunology

KMU-11342 is a potent inhibitor of multi-protein kinase. KMU-11342 plays an important inhibitor of rheumatoid arthritis (RA) research .
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Cat. No.: HY-106618
CAS No.: 13665-88-8
Synonyms: Ra 233
Research Areas:  

Cancer

Mopidamol (RA 233), a derivative of Dipyridamole (HY-B0312), is a phosphodiesterase inhibitor. Mopidamol can be used for non-small cell lung cancer (N-SCLC) research .
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Cat. No.: HY-135376
CAS No.: 345891-62-5
Purity:  98.76%
Target:  

Drug Derivative

Research Areas:  

Metabolic Disease

Atorvastatin methyl ester (Compound 2a) is a methyl esterified derivative of Atorvastatin. Atorvastatin methyl ester inhibits the 9-cis-RA-induced Gal4 reporter activity more strongly than Atorvastatin .
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Cat. No.: HY-121500
CAS No.: 355860-40-1
R-116010 is a potent and selective retinoic acid (RA) metabolism inhibitor and can inhibit hydroxylase CYP26. R-116010 can enhance the anti-tumor effect of retinoic acid drugs. R-116010 can be used for the research of cancer, metabolic and neurological disease, such as neuroblastoma .
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Cat. No.: HY-173071
Target:  

Bacterial

Research Areas:  

Infection

DprE1-IN-13 (Compound 42) is the inhibitor for decaprenyl-phosphoryl-β-d-ribose oxidase (DprE1) with IC50 of 12.72 μM. DprE1-IN-13 inhibits Mycobacterium tuberculosis H37Ra with MIC50 of 1.071 μM .
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Cat. No.: HY-125068
CAS No.: 218160-26-0
Research Areas:  

Inflammation/Immunology

RPR203494 is a potent inhibitor against CYP isozymes. RPR203494 shows inhibition against p38 kinase with an IC50 value of 9 nM and an EC50 value of 60 nM. RPR203494 demonstrates an inhibition of hepatic Cytochrome P450. RPR203494 is promising for research of rheumatoid arthritis (RA) .
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Cat. No.: HY-172397
Target:  

Bacterial

Research Areas:  

Infection

Mycobacterium Tuberculosis-IN-7 (Compound 4c) inhibits M. tuberculosis H37Ra with MIC of 5.34 μg/mL. Mycobacterium Tuberculosis-IN-7 exhibits slight cytotoxicity in cancer cell Vero, A549, and HepG2 (IC50s >50 μM) .
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Cat. No.: HY-151472
CAS No.: 3031666-31-3
Target:  

Carbonic Anhydrase

Research Areas:  

Infection

hCAIX/XII-IN-6 is an orally active carbonic anhydrase (CA) inhibitor. hCAIX/XII-IN-6 inhibits human CA isoforms hCA I, II, IV, IX, and XII with Ki values of 6697 nM, 2950 nM, 4093 nM, 4.1 nM and 7.7 nM, respectively. hCAIX/XII-IN-6 can be used for the research of rheumatoid arthritis (RA) .
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Cat. No.: HY-10291R
CAS No.: 51543-40-9
Synonyms: (R)-Flurbiprofen (Standard); MPC7869 (Standard)
Tarenflurbil (Standard) is the analytical standard of Tarenflurbil. This product is intended for research and analytical applications. Tarenflurbil ((R)-Flurbiprofen) is the R-enantiomer of the racemate NSAID Flurbiprofen, Tarenflurbil ((R)-Flurbiprofen) inhibits the binding of [3H]9-cis-RA to RXRα LBD with IC50 of 75 μM. Tarenflurbil can be used for Alzheimer's disease research.
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Cat. No.: HY-106019A
CAS No.: 145858-50-0
Synonyms: R75251 hydrochloride
Liarozole hydrochloride is an imidazole derivative and orally active retinoic acid (RA) metabolism-blocking agent (RAMBA). Liarozole hydrochloride inhibits the cytochrome P450 (CYP26)-dependent 4-hydroxylation of retinoic acid (IC50=7 μM), resulting in increased tissue levels of retinoic acid. Liarozole hydrochloride shows antitumoral properties .
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Cat. No.: HY-152035
CAS No.: 3033421-29-0
Target:  

Bacterial

Research Areas:  

Infection Inflammation/Immunology

Mycobacterial Zmp1-IN-1 is a mycobacterial zinc metalloprotease-1 (Zmp1) inhibitor. Mycobacterial Zmp1-IN-1 has anti-mycobacterial activity for Mtb H37Ra in dose-dependent inhibition. Mycobacterial Zmp1-IN-1 can be used for the research of tuberculosis (TB) .
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