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 37931 products of "Other Inhibitors"
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Pamiparib maleate
CAS:<p>Pamiparib (BGB-290) is a selective PARP inhibitor that blocks DNA repair and promotes apoptosis.</p>Formula:C44H42F2N8O14Purity:98%Color and Shape:SolidMolecular weight:944.859SGK1-IN-3
<p>SGK1-IN-3: Potent oral inhibitor of SGK1, may target osteoarthritis.</p>Formula:C23H20Cl2N6O3SColor and Shape:SolidMolecular weight:531.41Naltalimide
CAS:<p>Naltalimide: µ-opioid receptor partial agonist, improves bladder storage by affecting spinal cord reflex.</p>Formula:C28H28N2O5Purity:98%Color and Shape:SolidMolecular weight:472.53L 739749
CAS:<p>L 739749 is a CAAX peptidomimetic. It is also an inhibitor of farnesyl-protein transferase.</p>Formula:C24H41N3O6S2Purity:98%Color and Shape:SolidMolecular weight:531.73Retelliptine
CAS:<p>Retelliptine, a DNA topoisomerase II inhibitor, is used potentially for the treatment of cancer.</p>Formula:C25H32N4OPurity:98%Color and Shape:SolidMolecular weight:404.55AY-22,252
CAS:<p>AY-22,252 is an inhibitor of beef heart & rat brain nucleoside-3',5'- monophosphate phosphodiesterase.</p>Formula:C27H37NaO7Color and Shape:SolidMolecular weight:496.57Cytosaminomycin A
CAS:<p>Cytosaminomycin A is an antibiotic with anticoccidial and antibacterial properties.</p>Formula:C22H34N4O8SColor and Shape:SolidMolecular weight:514.592TP-6076
CAS:<p>TP-6076 is a fluorocycline antibiotic, inhibiting bacterial protein synthesis, exhibiting great antimicrobial activity against carbapenem-resistant A.</p>Formula:C28H32F3N3O7Color and Shape:SolidMolecular weight:579.56MEN-10354
CAS:<p>MEN-10354 is a less potent and less selective NK-2 tachykinin receptor antagonist compared to the linear analog, R 396.</p>Formula:C37H46N8O9Color and Shape:SolidMolecular weight:746.81Dehydroindapamide
CAS:<p>Dehydroindapamide, an indole form of Indapamide, is utilized to quantify the turnover rate of Indapamide in CYP3A4, which is approximately 10 times higher than that of Indoline, with slightly enhanced affinity for CYP3A4.</p>Formula:C16H14ClN3O3SColor and Shape:SolidMolecular weight:363.82Dehydelone
CAS:<p>Dehydelone(KOS-1584, R-1645, SK-10088) is a microtubule stabilizer that may be used in the treatment of non-small cell lung cancer.</p>Formula:C27H39NO5SColor and Shape:SolidMolecular weight:489.67Cycloepoxydon
CAS:<p>Cycloepoxydon inhibits the NF-KB and AP-1 mediated secretion of alkaline phosphatase (SEAP) induced by Phorbol 12-myristate 13-acetate (PMA), with IC50 values of 1-2 μg/mL (4.2-8.4 μM) and 3-5 μg/mL (12.6-21 μM), respectively.</p>Formula:C12H16O5Color and Shape:SolidMolecular weight:240.25212(S)-HEPE
CAS:<p>12(S)-HEPE, made from EPA by 12-LO, is an anti-inflammatory ω-3 derivative affecting leukotriene formation.</p>Formula:C20H30O3Color and Shape:SolidMolecular weight:318.45MB725
CAS:<p>MB725 is a strong and selective inducer of viability reduction in several cancer cell lines containing the oncogenic p53-Y220C mutation.</p>Formula:C18H21IN4O2SColor and Shape:SolidMolecular weight:484.35Calphostin I
CAS:<p>Calphostins, from Cladosporium fungus, inhibit PKC. Notably, calphostin C is a potent biochemical tool.</p>Formula:C44H38O15Color and Shape:SolidMolecular weight:806.76Antibiotic LL Z1640-2
CAS:<p>Antibiotic LL Z1640-2 is an inhibitor against the TAK1 activity.</p>Formula:C19H22O7Color and Shape:SolidMolecular weight:362.38Istamycin Y0
CAS:<p>Istamycin Y0 is an aminoglycoside antibiotic found in *Streptomyces tenjimariensis* [ATCC 31603]. This compound exhibits weak antibacterial activity against only a limited range of bacteria.</p>Formula:C14H30N4O4Color and Shape:SolidMolecular weight:318.413-IN-PP1
CAS:<p>3-IN-PP1: PKD inhibitor (IC50: 94-108 nM for PKD1/2/3), broad anticancer agent for research.</p>Formula:C17H18N6Color and Shape:SolidMolecular weight:306.36Porothramycin A
CAS:<p>Porothramycin A is an antibiotic effective against Gram-positive bacteria and anaerobic bacteria.</p>Formula:C18H21N3O4Color and Shape:SolidMolecular weight:343.377Nothramicin
CAS:<p>Nothramicin is an anthracycline antibiotic that exhibits antimycobacterial activity.</p>Formula:C30H37NO11Color and Shape:SolidMolecular weight:587.615MMP408
CAS:<p>MMP408 acts as an inhibitor of MMP-12.</p>Formula:C19H20N2O7SColor and Shape:SolidMolecular weight:420.44Dinordrin
CAS:<p>Dinordrin is an implantation inhibitor and hormone.</p>Formula:C27H36O4Purity:98%Color and Shape:SolidMolecular weight:424.57Epithienamycin C
CAS:<p>Epithienamycin C is a carbapenem antibiotic with activity against both Gram-positive and Gram-negative bacteria.</p>Formula:C13H18N2O5SColor and Shape:SolidMolecular weight:314.357Nanaomycin B
CAS:<p>Nanaomycin B is an antibiotic with activity against Gram-positive bacteria, mycobacteria, mycoplasma, and fungi.</p>Formula:C16H16O7Color and Shape:SolidMolecular weight:320.294MMG-11 quarterhydrate
<p>MMG-11 quarterhydrate, a potent hTLR2 antagonist, inhibits TLR2/1 and TLR2/6 with IC50s of 1.7μM and 5.7μM; low toxicity.</p>Formula:C15H16O8Color and Shape:SolidMolecular weight:310.781,6-Dihydroxy-2-chlorophenazine
CAS:<p>1,6-Dihydroxy-2-chlorophenazine exhibits weak antifungal and anti-yeast activity.</p>Formula:C12H7ClN2O2Color and Shape:SolidMolecular weight:246.65Tubulosine
CAS:<p>Tubulosine is an anticancer agent that inhibits cancer cell growth.</p>Formula:C29H37N3O3Color and Shape:SolidMolecular weight:475.62SSR-182289A (Free)
CAS:<p>SSR-182289A (Free) is a thrombin inhibitor.</p>Formula:C30H33F2N5O4SPurity:98%Color and Shape:SolidMolecular weight:597.68Reumycin
CAS:<p>Reumycin is a 7-azaindole antibiotic that exhibits cytotoxicity against tumor cells such as Ellrich carcinoma, Sarcoma-180, Sarcoma-37, and lymphosarcoma.</p>Formula:C6H5N5O2Color and Shape:SolidMolecular weight:179.136L 767679
CAS:<p>L 767679 is an antagonist of the fibrinogen receptors.</p>Formula:C20H24N4O4Purity:98%Color and Shape:SolidMolecular weight:384.43BRD-9526
CAS:<p>BRD-9526 is a potent and selective inhibitor of Sonic Hedgehog (Shh).</p>Formula:C26H31Cl2N3O6SPurity:98%Color and Shape:SolidMolecular weight:584.51Trypanothione synthetase-IN-4
<p>Trypanothione synthetase-IN-4, an L. infantum inhibitor, has potent anti-leishmanicidal properties (EC50: 0.6 μM).</p>Formula:C29H52INO2Color and Shape:SolidMolecular weight:573.63BAY-091
CAS:<p>BAY-091 is a novel potent and highly selective PIP4K2A kinase inhibitor.</p>Formula:C26H21FN4O2Purity:97.66% - 99.23%Color and Shape:SoildMolecular weight:440.479(R)-HETE
CAS:<p>9(R)-HETE, 50% of racemic mix, activates RXRγ 1.5x at 300 nM; identified by HPLC comparison.</p>Formula:C20H32O3Color and Shape:SolidMolecular weight:320.47Ici D1542
CAS:<p>Ici D1542: potent TXS inhibitor & TXA2 receptor antagonist, effective thromboxane blocker in vitro.</p>Formula:C25H30N2O7Purity:98%Color and Shape:SolidMolecular weight:470.5117β-HSD1-IN-1
<p>17β-HSD1-IN-1 (Compound 1) can be used in the non-small cell lung cancer (NSCLC) research.</p>Formula:C21H21NO3Color and Shape:SolidMolecular weight:335.4BM635 hydrochloride (1493762-74-5 free base)
<p>BM635 hydrochloride is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).</p>Formula:C25H30ClFN2OPurity:98%Color and Shape:SolidMolecular weight:428.97BMS-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:694.63AT-IAP
CAS:<p>AT-IAP is an effective dual antagonist of XIAP and cIAP1.</p>Formula:C29H40FN5O2Purity:98%Color and Shape:SolidMolecular weight:509.66ACSS2-IN-1
CAS:<p>ACSS2-IN-1, a potent ACSS2 inhibitor, has IC50 0.01-<1 nM; useful in cancer research.</p>Formula:C27H25ClN6O2Color and Shape:SolidMolecular weight:500.98B-3852
CAS:<p>B-3852 is a Bradykinin inhibitor.</p>Formula:C55H74F3N15O11Color and Shape:SolidMolecular weight:1178.27AKR1C3-IN-5
<p>AKR1C3-IN-5 inhibits AKR1C3, key in prostate/breast cancers, with MCF-7 cell IC50 of 9.6 μM.</p>Formula:C34H44N2O7Color and Shape:SolidMolecular weight:592.72Granaticin B
CAS:<p>Granaticin B inhibits the initial phase of RNA biosynthesis and exhibits activity against Gram-positive bacteria, mycobacteria (weak), and Trichomonas vaginalis, along with the ability to suppress tumor cells.</p>Formula:C28H30O12Color and Shape:SolidMolecular weight:558.531IDX-320
CAS:<p>IDX-320 is an HCV protease inhibitor.</p>Formula:C37H43F3N6O7S2Color and Shape:SolidMolecular weight:804.9MDL-27088
CAS:<p>MDL-27088 is an angiotensin-covering enzyme inhibitor.</p>Formula:C25H28N2O5Color and Shape:SolidMolecular weight:436.50GW311616
CAS:<p>GW-311616 is a long duration, orally bioavailable, and selective human neutrophil elastase (HNE) inhibitor (IC50: 22 nM; Ki: 0.31 nM).</p>Formula:C19H31N3O4SColor and Shape:SolidMolecular weight:397.53Dihydrokainic acid
CAS:<p>EAAT2(GLT1)-selective non-transportable inhibitor of L-glutamate and L-aspartate uptake</p>Formula:C10H17NO4Purity:98%Color and Shape:SolidMolecular weight:215.25LY3325656
CAS:<p>LY3325656, a GPR142 agonist with anti-diabetic properties, progresses to phase 1 trials for Type 2 diabetes.</p>Formula:C21H23F3N6O2Color and Shape:SolidMolecular weight:448.44nNOS-IN-25
CAS:<p>nNOS-IN-25 is an effective, selective, and cell-permeable inhibitor of neuronal nitric oxide synthase.</p>Formula:C21H22N4Purity:98%Color and Shape:SolidMolecular weight:330.43PREP inhibitor-1
CAS:<p>PREP inhibitor-1 is a prolyl oligopeptidase (PREP) inhibitor for the study of Alzheimer's disease.</p>Formula:C22H28N4O2Purity:98.78%Color and Shape:SoildMolecular weight:380.48
