
Other Inhibitors
This category encompasses a wide variety of inhibitors that do not fit into the standard classifications but are still critical for various biochemical and pharmacological research. These inhibitors may target unique or less-studied pathways, enzymes, and molecular interactions, providing valuable tools for specialized research areas. At CymitQuimica, we offer a diverse selection of high-quality inhibitors across multiple biological targets and research disciplines, enabling you to explore novel therapeutic avenues and deepen your understanding of complex biological processes.
Found 37928 products of "Other Inhibitors"
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Sapintoxin D
CAS:<p>Sapintoxin D is a fluorescent phorbol ester and selective activator of protein kinase C.</p>Formula:C30H37NO8Color and Shape:SolidMolecular weight:539.62ODN 21158
CAS:<p>ODN 21158 is a potent, non-cytotoxic inhibitor of G-modified TLR3 and TLR9. ODN 21158 dose-dependently inhibits IFN-α secretion.</p>Color and Shape:SolidONL-1204
CAS:<p>ONL-1204 is a small molecule, CD95 antigen inhibitor (Fas inhibitor) being developed by ONL Therapeutics for the treatment of retinal detachment.</p>Formula:C71H100N18O16Color and Shape:SolidMolecular weight:1461.66Fistupyrone
CAS:<p>Fistupyrone, an antibiotic, is a microbial metabolite found in Streptomyces (TP-A0569). It has the ability to inhibit infections caused by Alternaria brassicicola in Chinese cabbage.</p>Formula:C10H14O3Color and Shape:SolidMolecular weight:182.216BM635 mesylate (1493762-74-5 free base)
<p>BM635 mesylate is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).</p>Formula:C26H33FN2O4SPurity:98%Color and Shape:SolidMolecular weight:488.61Calphostin D
CAS:<p>Calphostins, PKC inhibitors from Cladosporium cladosporioides, include A, B, C, D, I; C is most potent.</p>Formula:C30H30O10Color and Shape:SolidMolecular weight:550.55Heparastatin
CAS:<p>Heparastatin is an inhibitor of heparanase.</p>Formula:C8H11F3N2O5Purity:98%Color and Shape:SolidMolecular weight:272.18Axl-IN-3
<p>Axl-IN-3 is a selective, potent and orally active inhibitor of AXL kinase (IC50: 41.5 nM) and has a low inhibitory effect on other kinases.</p>Formula:C24H25ClN6O2Color and Shape:SolidMolecular weight:464.952,4-Diaminoanisole
CAS:<p>2,4-Diaminoanisole is a carcinogenic aromatic primary amine compound.</p>Formula:C7H10N2OColor and Shape:SolidMolecular weight:138.17Heme Oxygenase-1-IN-2
<p>Heme Oxygenase-1-IN-2 is a novel inhibitor of heme oxygenase-1 (HO-1), displaying potent antiproliferative activity in vitro, with an IC50 value of 0.95 μM.</p>Formula:C19H18ClN3OColor and Shape:SolidMolecular weight:339.82Quinagolide Free Base
CAS:<p>Quinagolide Free Base is a non-ergot dopamine D(2)-agonist.</p>Formula:C20H33N3O3SColor and Shape:SolidMolecular weight:395.56SCP1-IN-2
<p>SCP1-IN-2: potent, selective SCP1 inhibitor; induces REST degradation, hinders its activity, may study REST-driven glioblastoma growth.</p>Formula:C19H17F3N2O6S2Color and Shape:SolidMolecular weight:490.47Octahydrocyclopenta[c]pyrrole
CAS:<p>Octahydrocyclopenta[c]pyrrole has demonstrated promising applications in the fields of anti-inflammatory, anti-tumor, and neuroprotection. The unique structure-activity relationship of Octahydrocyclopenta[c]pyrrole offers fresh insights for the design of new drugs.</p>Formula:C7H13NColor and Shape:SolidMolecular weight:111.18Ganciclovir monophosphonate
CAS:<p>Ganciclovir monophosphate treats CMV, inhibiting replication in human/animal strains (IC50: 0.01μM).</p>Formula:C10H16N5O6PColor and Shape:SolidMolecular weight:333.24GRPR antagonist-1
<p>GRPR antagonist-1 targets GRPR, kills specific cancer cells (e.g., PC3, Pan02, HGC-27), and promotes apoptosis by modulating Bcl-2 and Bax.</p>Formula:C29H33F3N4O4Color and Shape:SolidMolecular weight:558.59PD-149163
CAS:<p>PD-149163: brain-penetrating, selective NTR1 agonist; shows pro-cognitive, anti-psychotic, anxiolytic effects.</p>Formula:C42H71N9O6Color and Shape:SolidMolecular weight:798.07Phellinsin
CAS:<p>Phellinsin selectively inhibits the activity of chitin synthase I and II, with IC50 values of 76 and 28 μg/mL, respectively. It also exhibits antimicrobial effects against pathogens such as anthracnose, rice blast fungus, Aspergillus fumigatus, and Trichophyton mentagrophytes, with a MIC ranging from 12.5 to 50 μg/mL.</p>Formula:C18H14O8Color and Shape:SolidMolecular weight:358.30Revamilast sodium
CAS:<p>Revamilast sodium, also known as GRC4039 sodium, is a phosphodiesterase IV inhibitor for potentially treating of asthma and rheumatoid arthritis</p>Formula:C18H8Cl2F2N3NaO4Color and Shape:SolidMolecular weight:462.17Amidomycin
CAS:<p>Amidomycin is an antibiotic that primarily targets yeast.</p>Formula:C40H68N4O12Color and Shape:SolidMolecular weight:796.99NPEC-caged-(S)-3,4-DCPG
CAS:<p>mGlu8a agonist</p>Formula:C19H16N2O10Purity:98%Color and Shape:SolidMolecular weight:432.34Anticancer agent 28
<p>Anticancer agent 28 is 50x more potent than Oridonin, IC50 of 0.09 μM against K562; effective in H22 mouse tumors.</p>Formula:C28H33NO6Color and Shape:SolidMolecular weight:479.56Flavipucine
CAS:<p>Flavipucine (Flavipucin) is a glutarimide antibiotic found in the Aspergillus flavipes F-2090/7 strain. It exhibits antibacterial activity against Bacillus subtilis, possesses antiprotozoal properties, and demonstrates cytotoxic effects on various cancer cells.</p>Formula:C12H15NO4Color and Shape:SolidMolecular weight:237.252L-744832
CAS:<p>L-744832, also known as L-744,832, is a potent Farnesyltransferase inhibitor with potential anticancer activity.</p>Formula:C26H45N3O6S2Color and Shape:SolidMolecular weight:559.78DJT06001
CAS:<p>DJT06001 is a selective Factor Xa inhibitor, reducing thrombus formation with low risk of bleeding.</p>Formula:C21H20ClN3O5SColor and Shape:SolidMolecular weight:461.92CCW 28-3
CAS:<p>CCW 28-3 is a novel potent covalent BRD4 degrader, degrading BRD4 in a proteasome- and RNF4-dependent manner without inhibiting RNF4 autoubiquitination activity</p>Formula:C44H42Cl2N6O4SColor and Shape:SolidMolecular weight:821.81BMS-751324
CAS:<p>BMS-751324: p38α MAPK inhibitor with carbamyl-methyl, esters, phosphate from HPA. Reduces rat arthritis swelling and TNFα.</p>Formula:C32H35N6O10PColor and Shape:SolidMolecular weight:694.63Calphostin I
CAS:<p>Calphostins, from Cladosporium fungus, inhibit PKC. Notably, calphostin C is a potent biochemical tool.</p>Formula:C44H38O15Color and Shape:SolidMolecular weight:806.76ATR-IN-7
CAS:<p>ATR-IN-7 is a potent inhibitor of ATR.</p>Formula:C21H22FN7OColor and Shape:SolidMolecular weight:407.44SX 3202
CAS:<p>SX 3202 is an aldose reductase inhibitor being developed for the treatment of diabetic neuropathy.</p>Formula:C17H11BrFN3O4Color and Shape:SolidMolecular weight:420.19Porothramycin A
CAS:<p>Porothramycin A is an antibiotic effective against Gram-positive bacteria and anaerobic bacteria.</p>Formula:C18H21N3O4Color and Shape:SolidMolecular weight:343.377Odiparcil
CAS:<p>Odiparcil is an orally active beta-d-thioxyloside analog.</p>Formula:C15H16O6SPurity:98%Color and Shape:SolidMolecular weight:324.35Menoxymycin B
CAS:<p>Menoxymycin B is an antibiotic with cytotoxic properties, inhibiting KB and N18-RE-105 cells with IC50 values of 0.22 μM and 0.023 μM, respectively.</p>Formula:C25H31NO9Color and Shape:SolidMolecular weight:489.515NPR-C activator 1
CAS:<p>NPR-C activator 1 is an activator of the natriuretic peptide receptor C (NPR-C), which can be used to study cardiovascular diseases.</p>Formula:C18H24N6O3Purity:98.74%Color and Shape:SolidMolecular weight:372.42PARP1-IN-5
<p>PARP1-IN-5 is a potent, selective, orally active, low-toxicity PARP-1 inhibitor with an IC50 value of 14.7 nM. PARP1-IN-5 can be used in cancer research.</p>Formula:C25H24N2O5SColor and Shape:SolidMolecular weight:464.53Gusperimus
CAS:<p>Gusperimus was synthesized by chemical modification of spergualin and in combination with cyclosporine A to prevent diabetes in susceptible NOD mice.</p>Formula:C17H37N7O3Color and Shape:SolidMolecular weight:387.52Nurr1 agonist 1
<p>Nurr1 agonist 1 is an inverse agonist tool for the neuroprotective transcription factor Nurr1 which is an appealing target to treat neurodegenerative diseases.</p>Formula:C16H14N2O2Color and Shape:SolidMolecular weight:266.29GDC-6036-NH
CAS:<p>GDC-6036-NH is a precursor of compound 17a /b, which is a RAS inhibitor that can be used in cancer research.</p>Formula:C26H30ClF4N7OPurity:99.84%Color and Shape:SolidMolecular weight:568.01Ekatetrone
CAS:<p>Ekatetrone displays activity against both Gram-positive and Gram-negative bacteria, with particularly strong inhibitory effects on Mycobacterium tuberculosis.</p>Formula:C19H13NO7Color and Shape:SolidMolecular weight:367.30923-De(mycinosyloxy)tylosin
CAS:<p>23-De(mycinosyloxy)tylosin is a macrolide antibiotic exhibiting activity against Gram-positive bacteria, with limited efficacy against Gram-negative bacteria and mycoplasma.</p>Formula:C38H63NO12Color and Shape:SolidMolecular weight:725.91Pyrrolomycin A
CAS:<p>Pyrrolomycin A is a pyrrole antibiotic that exhibits activity against Gram-positive bacteria, Gram-negative bacteria, and fungi.</p>Formula:C4H2Cl2N2O2Color and Shape:SolidMolecular weight:180.977Peptaibolin
CAS:<p>Peptaibolin exhibits activity against Gram-positive bacteria and yeast. The minimum inhibitory concentration (MIC) for its effect on Bacillus subtilis [ATCC 6633] and Candida albicans is 100 μg/mL.</p>Formula:C31H51N5O6Color and Shape:SolidMolecular weight:589.77trans-Doxercalciferol
CAS:<p>trans-Doxercalciferol is an isomer of Doxercalciferol. Doxercalciferol is an activator of the Vitamin D receptor and prevents renal disease.</p>Formula:C28H44O2Purity:98%Color and Shape:SolidMolecular weight:412.65Exfoliazone
CAS:<p>Exfoliazone is a phenazinic antibiotic with activity against Trichoderma viride, exhibiting an ED50 for inhibiting mycelial growth of 70 μg/mL.</p>Formula:C15H12N2O4Color and Shape:SolidMolecular weight:284.267Mutalomycin
CAS:<p>Mutalomycin is a polyether antibiotic with activity against Gram-positive bacteria, mycoplasma, and coccidia.</p>Formula:C41H70O12Color and Shape:SolidMolecular weight:754.987Novokinin
CAS:<p>Angiotensin AT2 receptor agonist</p>Formula:C39H61N11O7Purity:98%Color and Shape:SolidMolecular weight:795.97FTI-2628
CAS:<p>FTI-2628 is a novel inhibitor of protein farnesyltransferase (FT), inhibiting the growth of P. falciparum in red blood cells and suppressing parasitemia.</p>Formula:C31H34N4O3SColor and Shape:SolidMolecular weight:542.69Chitinase-IN-4
<p>Chitinase-IN-4 (compound 8f) is a potent and selective inhibitor of OfChi-h with an IC50 value of 0.1 μM and good insecticidal activity.</p>Formula:C21H24ClN7Color and Shape:SolidMolecular weight:409.92AZD-4121 tert-butylammonium
CAS:<p>AZD-4121 tert-butylammonium is an oral cholesterol absorption inhibitor targeting NPC1L1 for the treatment of dyslipidaemia.</p>Formula:C40H50F2N4O7SColor and Shape:SolidMolecular weight:768.91Ro-24-4736
CAS:<p>Ro 24-4736 is an effective and selective platelet-activating factor antagonist.</p>Formula:C31H20ClN5OSPurity:98%Color and Shape:SolidMolecular weight:546.04Scorodonin
CAS:<p>SScorodonin exhibits antibacterial, antistreptomycete, and antifungal properties. It inhibits DNA-dependent RNA polymerase with an IC50 of 25 μg/mL.</p>Formula:C7H7ClOColor and Shape:SolidMolecular weight:142.583

