Inibitori
Gli inibitori sono molecole che si legano a enzimi, recettori o altre proteine per ridurre o bloccare la loro attività biologica. Questi composti sono ampiamente utilizzati nella ricerca per studiare le vie biologiche, comprendere i meccanismi delle malattie e sviluppare farmaci terapeutici. Gli inibitori svolgono un ruolo cruciale nel trattamento di varie malattie, tra cui il cancro, le malattie cardiovascolari e le infezioni. Presso CymitQuimica, offriamo una vasta gamma di inibitori di alta qualità per supportare le tue ricerche in biochimica, biologia cellulare e sviluppo farmaceutico.
Sottocategorie di "Inibitori"
- Angiogenesi(2.519 prodotti)
- Apoptosi(5.787 prodotti)
- Ciclo cellulare/Checkpoint(4.446 prodotti)
- Cromatina/Epigenetica(2.235 prodotti)
- Segnalazione citoscheletrica(1.381 prodotti)
- Danno al DNA/Riparazione del DNA(2.824 prodotti)
- Endocrinologia/Ormoni(3.500 prodotti)
- Enzima(3.639 prodotti)
- Proteina G/GPCR(8.318 prodotti)
- Immunologia e infiammazione(3.516 prodotti)
- Virus dell'influenza(296 prodotti)
- Segnalazione JAK/STAT(404 prodotti)
- Segnalazione MAPK(1.200 prodotti)
- Trasportatore di membrana/canale ionico(2.787 prodotti)
- Metabolismo(9.416 prodotti)
- Microbiologia/Virologia(6.968 prodotti)
- Neuroscienza(9.920 prodotti)
- Altri inibitori(37.928 prodotti)
- Ossidazione-riduzione(41 prodotti)
- Segnalazione PI3K/Akt/mTOR(1.400 prodotti)
- Proteasi/Proteasoma(1.596 prodotti)
- Cellule staminali e Derivati(831 prodotti)
- Adattatori Tirosin-chinasi(2.015 prodotti)
- Ubiquitinazione(1.649 prodotti)
Mostrare 16 più sottocategorie
Trovati 66627 prodotti di "Inibitori"
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Ceronapril
CAS:<p>Ceronapril (SQ 29852) is an orally active and potent angiotensin-converting enzyme (ACE) inhibitor (IC50 : 36 nM) for the study of dementia and hypertension.</p>Formula:C21H33N2O6PPurezza:97.94%Colore e forma:SolidPeso molecolare:440.47Glutaminyl Cyclase Inhibitor 4
CAS:<p>Glutaminyl Cyclase Inhibitor 4 is a potent, selective glutaminyl cyclase (QC) inhibitor (IC50: 6.1 nM). It is a potent anti-Alzheimer’s agent.</p>Formula:C22H33N5O3Purezza:98%Colore e forma:SolidPeso molecolare:415.53Ref: TM-T11423
Prodotto fuori produzionePL265
CAS:<p>PL265 is a long-acting dual ENKephalinase inhibitor (DENKi) with analgesic potential.</p>Formula:C27H35N2O9PPurezza:98%Colore e forma:SolidPeso molecolare:562.55FGFR1 inhibitor-10
CAS:<p>FGFR1 inhibitor-10 (Compound 4i), with an IC50 of 28 nM, effectively inhibits FGFR1 phosphorylation.</p>Formula:C26H30F3N7O2SPurezza:98%Colore e forma:SolidPeso molecolare:561.62Ref: TM-T79686
Prodotto fuori produzioneAlbuterol stearate
CAS:<p>Albuterol stearate, a salt form of Albuterol, is a selective beta2 agonist for treating asthma and COPD, with 29x preference for beta2 over beta1.</p>Formula:C31H57NO5Purezza:98%Colore e forma:SolidPeso molecolare:523.799Ref: TM-T25030
Prodotto fuori produzioneGR 218,231
CAS:<p>GR 218,231 is a selective antagonist of D3 dopamine receptor.</p>Formula:C24H33NO3SPurezza:98%Colore e forma:SolidPeso molecolare:415.59Ref: TM-T27431
Prodotto fuori produzione(E)-Crotylbarbital
CAS:<p>(E)-Crotylbarbital, a Crotylbarbital isomer, is a sedative with hypnotic, anticonvulsant properties, aiding sleep and mental stability.</p>Formula:C10H14N2O3Purezza:99.94%Colore e forma:SolidPeso molecolare:210.23Fosfonet sodium
CAS:<p>Fosfonet sodium is a sodium salt of phosphonoacetic acid, effective against herpesviruses by inhibiting viral DNA polymerase.</p>Formula:C2H4NaO5PColore e forma:SolidPeso molecolare:162.01Ref: TM-T69345
Prodotto fuori produzioneCK176
CAS:<p>CK176 is an HIV-1 inhibitor, 11x more effective than I-XW-053 in human PBMCs.</p>Formula:C21H12IN3O2Purezza:98%Colore e forma:SolidPeso molecolare:465.24Ref: TM-T27030
Prodotto fuori produzioneHPK1-IN-18
CAS:<p>HPK1-IN-18: Potent, specific inhibitor of HPK1, a MAP4K enzyme, for cancer research and treatment.</p>Formula:C24H24N4Colore e forma:LiquidPeso molecolare:368.47Ref: TM-T61449
Prodotto fuori produzioneJAK2-IN-9
CAS:<p>Compound A8, known as JAK2-IN-9, is a selective JAK2 inhibitor with an IC50 of 5 nM.</p>Formula:C20H24N6O2SPurezza:98%Colore e forma:SolidPeso molecolare:412.51Ref: TM-T79581
Prodotto fuori produzioneAminobutane bisphosphonate
CAS:<p>Aminobutane bisphosphonate curbs bone loss; may manage hypercalcemia in cancer.</p>Formula:C4H13NO6P2Colore e forma:SolidPeso molecolare:233.1Ref: TM-T69443
Prodotto fuori produzioneCH-100
CAS:<p>CH-100 is a Chinese herbal medicine previously used in the treatment of human hepatitis C.</p>Formula:C14H22ClNO3Colore e forma:SolidPeso molecolare:287.78Ref: TM-T30866
Prodotto fuori produzioneSB251023
CAS:<p>SB251023 is an agonist of β3-adrenoceptor.</p>Formula:C28H34NO6PColore e forma:SolidPeso molecolare:511.55DPX-3778
CAS:<p>DPX-3778, a triethanolamine salt, boosts tobacco callus growth 4-5x at 0.124-2.48 μM and slows aging with IAA and kinetin.</p>Formula:C16H23ClN4O6Colore e forma:SolidPeso molecolare:402.83Ref: TM-T31573
Prodotto fuori produzioneMitoE10
CAS:<p>MitoE10 is an effective mitochondrial targeting antioxidant.</p>Formula:C42H55O5PSColore e forma:SolidPeso molecolare:702.92Ref: TM-T33406
Prodotto fuori produzionePSB-6426
CAS:<p>PSB-6426 is the first potent and selective human nucleoside triphosphate diphosphohydrolase-2 inhibitor.</p>Formula:C22H29N4O10PPurezza:98%Colore e forma:SolidPeso molecolare:540.46Ref: TM-T24681
Prodotto fuori produzioneLp-PLA2-IN-15
CAS:<p>Lp-PLA2-IN-15 (example 2) is an inhibitor of lipoprotein-associated phospholipase A2 (Lp-PLA2) with potential application in Alzheimer's disease research [1].</p>Formula:C22H17F5N4O3Purezza:98%Colore e forma:SolidPeso molecolare:480.39Ref: TM-T79075
Prodotto fuori produzioneALPK1-IN-2
CAS:<p>ALPK1-IN-2 is a potent inhibitor of ALPK1 (α-kinase 1) (IC50: 95 nM). ALPK1-IN-2 inhibits NF-κB (IC50: 1.31 μM).</p>Formula:C20H18F2N4O2SColore e forma:SolidPeso molecolare:416.44Ref: TM-T62162
Prodotto fuori produzionePPARγ-IN-2
CAS:<p>"PPARγ-IN-2 (Compound 5a), a PPARγ inhibitor, exhibits an EC50 of 0.106 μM in inhibiting TG accumulation in 3T3-L1 preadipocytes.</p>Formula:C19H21N5OPurezza:98%Colore e forma:SolidPeso molecolare:335.4Ref: TM-T79678
Prodotto fuori produzioneLp-PLA2-IN-16
CAS:<p>Lp-PLA2-IN-16 (Example 1) is an inhibitor of lipoprotein-associated phospholipase A2 (Lp-PLA2) with potential applications in Alzheimer's disease research [1].</p>Formula:C22H17F5N4O3Purezza:98%Colore e forma:SolidPeso molecolare:480.39Ref: TM-T79076
Prodotto fuori produzioneCebranopadol ((1α,4α)stereoisomer)
CAS:<p>Cebranopadol ((1α,4α)stereoisomer) is a stereoisomer of cebranopadol which is a potent ORL-1 agonist.</p>Formula:C24H27FN2OPurezza:98%Colore e forma:SolidPeso molecolare:378.48Ref: TM-T10749
Prodotto fuori produzioneanti-TNBC agent-3
CAS:<p>Anti-TNBC agent-3 (compound 3g) is a compound that induces apoptosis and possesses anti-cancer cell proliferation properties.</p>Formula:C29H39F2N7OColore e forma:SolidPeso molecolare:539.66Ref: TM-T79410
Prodotto fuori produzioneH 35-25
CAS:<p>H 35-25 is a beta 2-antagonist.</p>Formula:C13H21NOColore e forma:SolidPeso molecolare:207.31Ref: TM-T70895
Prodotto fuori produzionePKUMDL-LTQ-301
CAS:PKUMDL-LTQ-301 is a potent inhibitor of HipA toxin. PKUMDL-LTQ-301 also inhibits E. coli persistence.Formula:C30H28N2O4Purezza:98%Colore e forma:SolidPeso molecolare:480.55Ref: TM-T28423
Prodotto fuori produzioneCulmerciclib
CAS:<p>Culmerciclib is a cell cycle protein-dependent kinase (CDK) inhibitor that exhibits antitumour effects.</p>Formula:C24H27FN8Colore e forma:SolidPeso molecolare:446.52Ref: TM-T62650
Prodotto fuori produzioneFostedil
CAS:<p>Fostedil enhances heart function, maintains blood flow during partial/total coronary occlusions, and lowers aortic pressure.</p>Formula:C18H20NO3PSPurezza:98%Colore e forma:SolidPeso molecolare:361.4Ref: TM-T27351
Prodotto fuori produzionePS372424 HCl
CAS:<p>PS372424 activates CXCR3, triggers ERK phosphorylation, and inhibits CXCL11's effect on CD45+ cell migration in humanized mice.</p>Formula:C33H45ClN6O4Colore e forma:SolidPeso molecolare:625.21Ref: TM-T70411
Prodotto fuori produzioneLp-PLA2-IN-12
CAS:<p>Lp-PLA2-IN-12 (compound 19), an Lp-PLA2 inhibitor, is utilized in researching neurodegenerative diseases including Alzheimer's disease (AD), glaucoma, age-</p>Formula:C24H23F2N5O3Purezza:98%Colore e forma:SolidPeso molecolare:467.47Ref: TM-T79010
Prodotto fuori produzioneSR14150
CAS:<p>SR14150 is a partial agonist of high-affinity NOP receptor.</p>Formula:C21H30N2OPurezza:98%Colore e forma:SolidPeso molecolare:326.48Ref: TM-T24828
Prodotto fuori produzioneErythrityl Tetranitrate
CAS:<p>Erythrityl Tetranitrate, a vasodilator similar to nitroglycerin, was first in "sustained release" tablets; may cause "nitro headache."</p>Formula:C4H6N4O12Colore e forma:SolidPeso molecolare:302.11Ref: TM-T31671
Prodotto fuori produzioneBET-IN-15
CAS:<p>BET-IN-15 (compound 1) is a potent, orally active inhibitor of BET, demonstrating inhibitory IC50 values of 0.64 nM for BRD4-BD1 and 0.25 nM for BRD4-BD2.</p>Formula:C21H18F2N4O3SPurezza:98%Colore e forma:SolidPeso molecolare:444.45Ref: TM-T79167
Prodotto fuori produzioneAEF0117
CAS:<p>AEF0117 is a signaling inhibitor of CB1-SSi that inhibits cannabinoid self-administration and can be used to study cannabis withdrawal.</p>Formula:C29H40O3Purezza:99.58%Colore e forma:SolidPeso molecolare:436.63HBV-IN-38
CAS:<p>HBV-IN-38 (Example 193), an HBV DNA inhibitor with an EC50 value of ≤100 nM, serves as a research tool for investigating viral infections [1].</p>Formula:C18H16F3N5O4S2Purezza:98%Colore e forma:SolidPeso molecolare:487.48Antitumor photosensitizer-2
CAS:<p>Compound 11, also known as Antitumor Photosensitizer-2, is a potent photosensitizer with remarkable photodynamic anti-tumor properties and minimal skin photo-</p>Formula:C40H47N5O7Colore e forma:SolidPeso molecolare:709.83Mal-cyclohexane-Gly-Gly-Phe-Gly-Exatecan
CAS:<p>Mal-cyclohexane-Gly-Gly-Phe-Gly-Exatecan is a linker molecule employed in the synthesis of antibody-drug conjugates (ADCs), demonstrating potent antitumor</p>Formula:C55H60FN9O13Colore e forma:SolidPeso molecolare:1074.12Cap-dependent endonuclease-IN-9
CAS:<p>Cap-dependent endonuclease-IN-9, a strong influenza inhibitor, shows low toxicity, good pharmacokinetics, and dynamic action.</p>Formula:C29H22F2N4O7SPurezza:98%Colore e forma:SolidPeso molecolare:608.57Ref: TM-T72125
Prodotto fuori produzionediMal-O-CH2COOH
CAS:<p>DiMal-O-CH2COOH is a cleavable linker utilized in antibody-drug conjugates (ADCs).</p>Formula:C13H12N2O7Colore e forma:SolidPeso molecolare:308.24JAK1-IN-11
CAS:<p>JAK1-IN-11 (compound 11) serves as a potent inhibitor of Janus kinases, exhibiting nanomolar inhibitory concentrations with IC50 values of 0.02 nM (JAK1) and 0.</p>Formula:C26H36N6O4SPurezza:98%Colore e forma:SolidPeso molecolare:528.67Tibremciclib
CAS:<p>Tibremciclib is a cyclin-dependent kinase 4 (CDK4) inhibitor that exhibits antineoplastic properties [1].</p>Formula:C28H32F2N8Purezza:98%Colore e forma:SolidPeso molecolare:518.6Mal-VC-PAB-PNP-CDN-A
CAS:<p>Mal-VC-PAB-PNP-CDN-A is a conjugate comprised of an agent and a linker, utilized in antibody-drug conjugates (ADC) [1] [2].</p>Formula:C51H67N17O20P2Colore e forma:SolidPeso molecolare:1300.13FAP-IN-2
CAS:<p>FAP-IN-2 is a 99mTc-labeled, isonitrile-containing derivative of a fibroblast activation protein (FAPI) inhibitor suitable for tumor imaging [1].</p>Formula:C24H28F2N6O3Colore e forma:SolidPeso molecolare:486.51SARS-CoV-2-IN-68
CAS:<p>SARS-CoV-2-IN-68 (compound 6C) is a covalent inhibitor of both SARS-CoV-2 PLpro and Mpro, exhibiting potent antiviral properties by targeting the Zn-finger</p>Formula:C14H12N2OSePurezza:98%Colore e forma:SolidPeso molecolare:303.22PF-05236216 hydrochloride
CAS:<p>PF-05236216 hydrochloride: Brain-penetrant, potent CK1δ/ε inhibitor affecting mouse circadian rhythms.</p>Formula:C18H15FN4OColore e forma:SolidPeso molecolare:322.34Ref: TM-T70812
Prodotto fuori produzioneBTK-IN-27
CAS:<p>BTK-IN-27 (example 8), a potent BTK inhibitor with an IC50 of 0.2 nM, demonstrates anti-proliferative effects in TMD8 cells with an IC50 of less than 5 nM.</p>Formula:C31H35N7O2Purezza:98%Colore e forma:SolidPeso molecolare:537.66Canlitinib
CAS:<p>Canlitinib, a tyrosine kinase inhibitor, holds potential for cancer research.</p>Formula:C33H31F2N3O7Purezza:98%Colore e forma:SolidPeso molecolare:619.61VISTA-IN-2
CAS:<p>VISTA-IN-2 (Compound 1) is a V-domain Ig suppressor of T-cell activation (VISTA) inhibitor that promotes the degradation of VISTA in cells via autophagy,</p>Formula:C23H23N3OPurezza:98%Colore e forma:SolidPeso molecolare:357.45Ref: TM-T79653
Prodotto fuori produzioneCYY292
CAS:<p>CYY292 is a chemical compound acting as an inhibitor of PDGFRα, PDGFRβ, FGFR1, -2, and -3, with respective IC50 values of 5.35, 4.6, 28, 28, and 78 nM.</p>Formula:C24H28N8OColore e forma:SolidPeso molecolare:444.53YK-029A
CAS:<p>YK-029A, an orally active EGFR mutant inhibitor, targets both EGFR T790M and EGFRex20ins mutations.</p>Formula:C27H32N8O2Purezza:98%Colore e forma:SolidPeso molecolare:500.6Ref: TM-T79461
Prodotto fuori produzione(αR)-Cyclopropaneacetamide-Exatecan
CAS:<p>(αR)-Cyclopropaneacetamide-Exatecan (compound 2-A), an Exenotecan derivative, serves as a cytotoxic agent that effectively inhibits the proliferation of U87MG</p>Formula:C29H28FN3O6Colore e forma:SolidPeso molecolare:533.55JAK-IN-34
CAS:<p>JAK-IN-34 (compound 11n) is a potent inhibitor of Janus kinases (JAKs), demonstrating IC50 values of 0.40 nM for JAK1, 0.83 nM for JAK2, 2.10 nM for JAK3,</p>Formula:C27H26N6OPurezza:98%Colore e forma:SolidPeso molecolare:450.53MDVN1003
CAS:<p>MDVN1003 inhibits BTK & PI3Kδ in B cells, blocking NHL growth; it kills lymphoma cells, not erythroblasts.</p>Formula:C22H20FN7OPurezza:98%Colore e forma:SolidPeso molecolare:417.44Ref: TM-T28008
Prodotto fuori produzioneTauro-Obeticholic Acid sodium
CAS:<p>Tauro-obeticholic acid, a farnesoid X receptor (FXR) agonist and semisynthetic derivative of chenodeoxycholic acid, is an active metabolite of obeticholic acid.</p>Formula:C28H48NO6S·NaColore e forma:SolidPeso molecolare:549.74CGP 56999A
CAS:<p>CGP 56999A is a GABA(B) receptor antagonist; it boosts BDNF and reduces dopamine loss in rat striatum.</p>Formula:C19H30NO5PPurezza:98%Colore e forma:SolidPeso molecolare:383.42Ref: TM-T26993
Prodotto fuori produzioneFOXM1-IN-2
CAS:<p>FOXM1-IN-2, a FOXM1 inhibitor, exhibits antineoplastic activity [1].</p>Formula:C48H47F4N7O12SColore e forma:SolidPeso molecolare:1021.99URAT1 inhibitor 5
CAS:<p>URAT1 Inhibitor 5 (compound 16) serves as a powerful inhibitor of URAT1 and is utilized in hyperuricemia research [1].</p>Formula:C18H14BrN3O2SColore e forma:SolidPeso molecolare:416.29VMAT2-IN-2 tosylate
CAS:<p>VMAT2-IN-2 tosylate is a potent inhibitor of VMAT2 and is applicable in the research of tardive dyskinesia [1].</p>Formula:C27H36F3NO6SPurezza:98%Colore e forma:SolidPeso molecolare:559.64Ref: TM-T79061
Prodotto fuori produzioneDiaFluo
CAS:<p>DiaFluo is a probe for protein S-sulfinylation from cells.</p>Formula:C32H32N4O9SColore e forma:SolidPeso molecolare:648.69Xilmenolone
CAS:<p>Xilmenolone acts as a positive allosteric modulator of the GABA_A receptor [1].</p>Formula:C26H37N3O2Purezza:98%Colore e forma:SolidPeso molecolare:423.59Ref: TM-T78670
Prodotto fuori produzioneAntibacterial agent 157
CAS:<p>Compound B12 (Antibacterial agent 157) is a fungicidal agent that can impact protein synthesis in Botrytis cinerea.</p>Formula:C26H23BrF4N2O3Colore e forma:SolidPeso molecolare:567.37Davelizomib
CAS:<p>Davelizomib is a proteasome inhibitor that exhibits antineoplastic activity [1].</p>Formula:C21H26BF2N3O7Purezza:98%Colore e forma:SolidPeso molecolare:481.25MOR agonist-1
CAS:<p>MOR Agonist-1 is a μ-opioid receptor (MOR) agonist noted for its potent analgesic properties and is utilized in research concerning pain and associated</p>Formula:C22H26ClFN2O2Purezza:98%Colore e forma:SolidPeso molecolare:404.91URAT1&XO inhibitor 1
CAS:<p>URAT1&XO Inhibitor 1 (compound 29) serves as a dual inhibitor with IC50 values of approximately 10 μM for URAT1 and 1.01 μM for Xanthine Oxidase.</p>Formula:C20H13N5O3SPurezza:98%Colore e forma:SolidPeso molecolare:403.41Ref: TM-T79175
Prodotto fuori produzioneBelfosdil
CAS:<p>Belfosdil is a blocker of antihypertensive calcium channel.</p>Formula:C27H50O7P2Purezza:98%Colore e forma:SolidPeso molecolare:548.63Ref: TM-T26764
Prodotto fuori produzioneBBDDL2059
CAS:<p>BBDDL2059 is a selective covalent inhibitor targeting EZH2, exhibiting an IC50 of 1.5 nM against the EZH2-Y641F mutant.</p>Formula:C27H36N4O4SPurezza:98%Colore e forma:SolidPeso molecolare:512.66Ref: TM-T79200
Prodotto fuori produzioneBi-Mc-VC-PAB-MMAE
CAS:<p>Bi-Mc-VC-PAB-MMAE is an agent-linker conjugate for antibody-drug conjugates (ADCs), featuring the linker (Fmoc-Val-Cit-PAB) and the potent tubulin inhibitor (</p>Formula:C71H104N12O18Colore e forma:SolidPeso molecolare:1413.66LT-540-717
CAS:<p>LT-540-717 (compound 32), a potent FLT3 inhibitor (IC50=0.62 nM), exhibits antiproliferative activity and effectively inhibits various acquired FLT3 mutations,</p>Formula:C24H24N8O2Colore e forma:SolidPeso molecolare:456.5Ref: TM-T79490
Prodotto fuori produzioneLerzeparib
CAS:<p>Lerzeparib is a PARP (ADP-ribose polymerase) inhibitor that exhibits antineoplastic activity [1].</p>Formula:C21H20FN3O2Purezza:98%Colore e forma:SolidPeso molecolare:365.4DPP
CAS:<p>DPP, a Platinum(IV) complex with a pterostilbene-derived axial ligand, inhibits the JAK2-STAT3 pathway in breast cancer (BC) cells, demonstrating</p>Formula:C36H40Cl2N2O10PtPurezza:98%Colore e forma:SolidPeso molecolare:926.7DDO-2213
CAS:<p>DDO-2213 is a potent, orally active inhibitor of the WDR5-MLL1 interaction, demonstrating an IC50 of 29 nM and a Kd of 72.9 nM against WDR5.</p>Formula:C24H27ClFN7OColore e forma:SolidPeso molecolare:483.97Antibacterial agent 160
CAS:<p>Antibacterial Agent 160 is a potent antibacterial agent that rapidly eradicates bacteria and inhibits the formation of bacterial biofilms.</p>Formula:C29H27ClFN3O6Colore e forma:SolidPeso molecolare:567.99Estrogen receptor modulator 8
CAS:<p>Estrogen Receptor Modulator 8 (compound 4) is an orally active inhibitor targeting Estrogen Receptor/ERR α with potent efficacy (IC50 = 0.437 nM in MCF-7 cells</p>Formula:C25H24F4N2O2Purezza:98%Colore e forma:SolidPeso molecolare:460.46RIOK2-IN-2
CAS:<p>RIOK2-IN-2 (8) functions as an inhibitor of RIOK2, exhibiting IC50 values of 3.02 μM in MKN-1 cells and 5.34 μM in MOLT4 cells [1].</p>Formula:C27H23F3N6O2Colore e forma:SolidPeso molecolare:520.51And1-IN-1
CAS:<p>And1-IN-1, also known as compound III, is a potent inhibitor of And1 [1].</p>Formula:C15H11BCl2O2Colore e forma:SolidPeso molecolare:304.96ROCK2-IN-6
CAS:<p>ROCK2-IN-6 (Comp A) is a selective inhibitor of ROCK2, applicable in the study and treatment of ROCK-mediated, autoimmune, and inflammatory diseases [1].</p>Formula:C26H21F2N7OPurezza:98%Colore e forma:SolidPeso molecolare:485.49S-72
CAS:<p>S-72 acts as a microtubule polymerization inhibitor, effective in cell-free assays at concentrations of 1, 3, and 10 µM.</p>Formula:C20H22N4O3SColore e forma:SolidPeso molecolare:398.50Ref: TM-T83874
Prodotto fuori produzioneL 689037
CAS:<p>L 689037 is an inhibitor of leukotriene biosynthesis.</p>Formula:C36H37ClN2O4Purezza:98%Colore e forma:SolidPeso molecolare:597.14Ref: TM-T24337
Prodotto fuori produzioneBET-IN-14
CAS:<p>BET-IN-14 is a pan BET inhibitor with an IC50 of 5.35 nM, demonstrating oral activity and anticancer properties [1].</p>Formula:C30H37N7O2Purezza:98%Colore e forma:SolidPeso molecolare:527.66FLT3-IN-19
CAS:<p>FLT3-IN-19 (Comp 50) is a potent, selective inhibitor of FLT3, demonstrating an IC50 value of 0.213 nM, and is applicable in research pertaining to acute</p>Formula:C22H26N8OColore e forma:SolidPeso molecolare:418.49ALPK1-IN-3
CAS:<p>ALPK1-IN-3,serves as an ALPK1 inhibitor that dampens proinflammatory gene expression in the kidney and enhances survival in animal models of sepsis-induced</p>Formula:C20H16F2N4OSPurezza:98%Colore e forma:SolidPeso molecolare:398.43Antitumor photosensitizer-1
CAS:<p>Antitumor Photosensitizer-1 (Compound 8) is a potent photosensitizer with remarkable photodynamic anti-tumor properties and minimal skin photo-toxicity,</p>Formula:C42H51N5O6Colore e forma:SolidPeso molecolare:721.88PI3Kδ-IN-13
CAS:<p>PI3Kδ-IN-13 (compound 89), with an IC50 value of 2.6 nM, is an inhibitor of PI3Kδ, applicable for researching diseases involving cell proliferation, including</p>Formula:C27H39N7O4S2Colore e forma:SolidPeso molecolare:589.77I-BET282
CAS:<p>BET-IN-1 is a bromodomain inhibitor extracted from patent WO/2013024104A1 (example 2, plC50: 6.0 - 7.0).</p>Formula:C25H30N4O4Purezza:98%Colore e forma:SolidPeso molecolare:450.53Antitumor agent-104
CAS:<p>Antitumor Agent-104 (Compound 9) serves as an antineoplastic by impeding DNA repair mechanisms in tumor cells, primarily through the inhibition of PARP1 enzyme</p>Formula:C31H33FN6O3Purezza:98%Colore e forma:SolidPeso molecolare:556.63ATR-IN-24
CAS:<p>ATR-IN-24 (Compound 1) is an ATR inhibitor with demonstrated anticancer activity [1].</p>Formula:C23H26N6O2Purezza:98%Colore e forma:SolidPeso molecolare:418.49Ref: TM-T79058
Prodotto fuori produzioneSakura 6
CAS:<p>Sakura 6, a synthetic serotonin transporter (SERT)-binding peptide, enhances the interaction between SERT and neuronal nitric oxide synthase.</p>Formula:C31H45N5O7Colore e forma:SolidPeso molecolare:599.73LFS-1107
CAS:<p>LFS-1107, a reversible CRM1 inhibitor (Kd: 12.5 pM), selectively targets and eliminates ENKTL cells, offering potential for cancer research applications [1].</p>Formula:C12H11N5OS2Purezza:98%Colore e forma:SolidPeso molecolare:305.38HPK1-IN-38
CAS:<p>HPK1-IN-38 (compound 15) is an inhibitor of MAP4K1/HPK1, suitable for research into disorders related to HPK1 [1].</p>Formula:C29H29N5O3Colore e forma:SolidPeso molecolare:495.57CIAC001
CAS:<p>CIAC001, a pyruvate kinase PKM2 inhibitor, exhibits anti-neuroinflammatory properties.</p>Formula:C20H25N3O2Colore e forma:SolidPeso molecolare:339.43Ref: TM-T79637
Prodotto fuori produzioneAPG-2449
CAS:<p>APG-2449 is an orally active inhibitor targeting ALK, ROS1, and FAK, demonstrating antitumor efficacy in mouse models of non-small cell lung cancer (NSCLC) [1].</p>Formula:C33H42ClN5O4SPurezza:98%Colore e forma:SolidPeso molecolare:640.24Ref: TM-T79363
Prodotto fuori produzioneJDB175
CAS:<p>JDB175, a selective BTK inhibitor with oral bioavailability, demonstrates excellent penetration through the blood-brain barrier.</p>Formula:C26H21F3N4O2Purezza:98%Colore e forma:SolidPeso molecolare:478.47IDO1-IN-22
CAS:<p>IDO1-IN-22 (Compound 3) is an inhibitor of IDO1, demonstrating potent activity with biochemical hIDO1 IC50 of 67.4 nM and HeLa hIDO1 IC50 of 17.6 nM.</p>Formula:C12H12BrFN6O3Purezza:98%Colore e forma:SolidPeso molecolare:387.16Igermetostat
CAS:<p>Igermetostat, an EZH2 inhibitor, is utilized both in vivo and in vitro for cancer research [1].</p>Formula:C32H46N4O4Purezza:98%Colore e forma:SolidPeso molecolare:550.73LM2I
CAS:<p>LM2I, a derivative of Spinosyn A (SPA), serves both as an argininosuccinate synthase (ASS1) enzyme activator and a tumor inhibitor through direct interaction</p>Formula:C47H77N3O11Colore e forma:SolidPeso molecolare:860.13Civorebrutinib
CAS:<p>Civorebrutinib (WS-413) is an inhibitor of Bruton's tyrosine kinase that exhibits antineoplastic activity [1].</p>Formula:C23H22ClN7O2Colore e forma:SolidPeso molecolare:463.92Immune cell migration-IN-1
CAS:<p>Immune cell migration-IN-1 (compound 2) serves as a potent inhibitor of immune cell migration, with potential research applications for mitigating conditions</p>Formula:C30H25ClN4O6SColore e forma:SolidPeso molecolare:605.06Yhhu6669
CAS:<p>Yhhu6669 is an anti-HBV agent that suppresses viral DNA and replication by promoting DNA-free capsid assembly, effectively reducing HBV DNA and HBcAg levels in</p>Formula:C29H28ClFN6O3Purezza:98%Colore e forma:SolidPeso molecolare:563.02Ref: TM-T78756
Prodotto fuori produzioneIDO/Tubulin-IN-2
CAS:<p>IDO/Tubulin-IN-2 inhibits TDO/tubulin, effective on U87, HepG2, A549, HCT-116, LO2 cancer cells; IC50 values 0.036-1.04 μM, boosts antitumor action.</p>Formula:C48H40N6O10Colore e forma:SolidPeso molecolare:860.87Ref: TM-T74536
Prodotto fuori produzioneAzilsartan mepixetil potassium
CAS:<p>Azilsartan medoxomil potassium (QR-01019K), an angiotensin II receptor antagonist, exhibits a potent and sustained antihypertensive effect, along with a more</p>Formula:C36H33KN6O8Colore e forma:SolidPeso molecolare:716.78EST73502
CAS:<p>EST73502 is a compound that functions as a dual agonist for the μ-opioid receptor (MOR) and an antagonist for the σ1 receptor (σ1R). It is selective, orally active, and possesses the ability to penetrate the blood-brain barrier (BBB). The compound exhibits a Ki value of 64 nM for the MOR and 118 nM for the σ1R. Additionally, EST73502 demonstrates antinociceptive activity [1].</p>Formula:C19H26F2N2O2Purezza:98%Colore e forma:SolidPeso molecolare:352.426
