Inhibitors
Inhibitors are molecules that bind to enzymes, receptors, or other proteins to reduce or block their biological activity. These compounds are widely used in research to study biological pathways, understand disease mechanisms, and develop therapeutic drugs. Inhibitors play a crucial role in the treatment of various diseases, including cancer, cardiovascular diseases, and infections. At CymitQuimica, we provide a diverse range of high-quality inhibitors to support your research in biochemistry, cell biology, and pharmaceutical development.
Subcategories of "Inhibitors"
- Angiogenesis(2,765 products)
- Apoptosis(6,237 products)
- Cell Cycle/Checkpoint(4,778 products)
- Chromatin/Epigenetics(2,426 products)
- Cytoskeletal Signaling(1,515 products)
- DNA Damage/DNA Repair(2,957 products)
- Endocrinology/Hormones(3,692 products)
- Enzyme(3,665 products)
- GPCR/G-Protein(8,968 products)
- Immunology and Inflammation(3,857 products)
- Influenza Virus(301 products)
- JAK/STAT signaling(413 products)
- MAPK Signaling(1,249 products)
- Membrane Transporter/Ion Channel(3,024 products)
- Metabolism(10,184 products)
- Microbiology/Virology(7,551 products)
- Neuroscience(10,359 products)
- Other Inhibitors(36,088 products)
- Oxidation-Reduction(43 products)
- PI3K/Akt/mTOR Signaling(1,444 products)
- Proteases/Proteasome(1,718 products)
- Stem Cell and Derivatives(825 products)
- Tyrosine Kinase/Adaptors(2,035 products)
- Ubiquitination(1,710 products)
Show 16 more subcategories
Found 66669 products of "Inhibitors"
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Tetramethylrhodamine-5-iodoacetamide
CAS:5-TMRIA: thiol-selective dye; labels proteins at cysteine residues; covalently marks DNA.Formula:C26H24IN3O4Purity:98%Color and Shape:SolidMolecular weight:569.39E3 ligase Ligand 13
E3 ligase Ligand 13, used for PROTACs making, induces degradation of cancer proteins via ubiquitination.Formula:C31H34N2O6Purity:98%Color and Shape:SolidMolecular weight:530.61Plozalizumab
CAS:<p>Plozalizumab (MLN-1202) is a humanized selective and potent anti-CCR2 antibody.Plozalizumab has antitumor activity.Plozalizumab is used in the study of</p>Purity:96.4%Color and Shape:LiquidMolecular weight:146.02 kDaSulfo-Cy5.5 ethylenediamine
Sulfo-Cyanine5.5 is a water soluble cyanine dye for far red / NIR applications such as in vivo imaging.Formula:C43H47K3N4O14S4Purity:98%Color and Shape:SolidMolecular weight:1089.41SJ1008030 TFA
SJ1008030 (compound 8) TFA is a selective JAK2-degrading PROTAC that inhibits the growth of MHH-CALL-4 leukemia cells with an IC50 of 5.4 nM, indicating itsFormula:C44H44F3N13O9SPurity:98%Color and Shape:SolidMolecular weight:987.96Sanggenon N
CAS:Sanggenon N protects against oxidative stress, EC50 of 23.45 ± 4.72 uM, and blocks NO in macrophages.Formula:C25H26O6Purity:98%Color and Shape:SolidMolecular weight:422.477Thiol-PEG-CH2COOH (MW 3400)
Thiol-PEG-CH2COOH (MW 3400) is a Polyethylene Glycol (PEG) derivative employed as a PROTAC linker for PROTAC synthesis[1].Purity:98%Color and Shape:SolidMolecular weight:N/AH4R antagonist 3
CAS:H4R antagonist 3 is a novel histamine-4 receptor (H4R) antagonist with an EC50 <10 mM.H4R antagonist 3 has potential inflammatory activity for the study ofFormula:C19H21ClN4SPurity:98%Color and Shape:SolidMolecular weight:372.92Prionitin
CAS:Prionitin is a natural product from Salvia prionitis Hance.Formula:C21H26O2Purity:98%Color and Shape:SolidMolecular weight:310.43BCN-PEG3-Val-Cit
BCN-PEG3-Val-Cit is a PEG linker used in PROTAC creation and ADCs as a cleavable unit.Formula:C31H51N5O10Purity:98%Color and Shape:SolidMolecular weight:653.76SPR741 TFA (1179330-52-9 free base)
<p>SPR741 TFA (NAB741 TFA) is a cationic peptide derived from polymyxin B and is a potentiator molecule.</p>Formula:C46H74F3N13O15Purity:98%Color and Shape:SolidMolecular weight:1106.15D-JBD19
CAS:D-JBD19 is a non-permeable peptide with neuroprotective effects.Formula:C99H164N32O28Purity:98%Color and Shape:SolidMolecular weight:2250.597Amino-PEG36-acid
CAS:Amino-PEG36-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules.Formula:C75H151NO38Purity:98%Color and Shape:SolidMolecular weight:1674.99Ac-AAVALLPAVLLALLAP-YVAD-CHO
CAS:Ac-AAVALLPAVLLALLAP-YVAD-CHO is a cell-permeable inhibitor of caspase-1 exhibiting antitumor activity [1].Formula:C97H160N20O24Purity:98%Color and Shape:SolidMolecular weight:1990.43MST-312
CAS:<p>MST-312, a telomerase inhibitor derived from green tea's EGCG, has research potential in cancer, including MM.</p>Formula:C20H16N2O6Purity:99.61% - 99.68%Color and Shape:SolidMolecular weight:380.35Imitrodast
CAS:Imitrodast is a small molecule thromboxane A2 synthase (TXA2 synthase) inhibitor for the treatment of immune system disorders, respiratory disorders, andFormula:C13H12N2O2SPurity:98.39%Color and Shape:SolidMolecular weight:260.31Rhuscholide A
CAS:Rhuscholide A possesses significant anti-HIV-1 activity with an EC50 value of 1.62 microM and a therapeutic index (TI) of 42.40.Formula:C31H42O3Purity:98%Color and Shape:SolidMolecular weight:462.66BKM1644
CAS:BKM1644 is an effective inhibition of the proliferation of metastatic, castration-resistant PCa (mCRPC) cells.Formula:C34H37Cl2F5N2O9P2Purity:98%Color and Shape:SolidMolecular weight:845.51Raddeanoside R17
CAS:Raddeanoside R17 is a natural product for research related to life sciences. The catalog number is TN4863 and the CAS number is 824401-07-2.Formula:C71H116O35Purity:98%Color and Shape:SolidMolecular weight:1529.66PROTAC FAK degrader 1
CAS:<p>PROTAC FAK degrader 1 is a selective and potent degrader of focal adhesion kinase (Fak) (IC50 of 6.5 nM).</p>Formula:C47H56F3N9O8S2Purity:98%Color and Shape:SolidMolecular weight:996.13
