CymitQuimica ha oltre 25 partner, tra i quali spicca il fornitore TargetMol
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UR-MB108
CAS:UR-MB108 is a potent and selective inhibitor of ABCG2 (BCRP), displaying an IC50 value of 79 nM, and exhibits stability in blood plasma.Formula:C40H38N6O4Colore e forma:SolidPeso molecolare:666.77Kinetin riboside
CAS:Kinetin riboside (N6-Furfuryladenosine) can induce apoptosis in cancer cells. It inhibits the proliferation of HCT-15 cells(IC50 of 2.5 μM)Formula:C15H17N5O5Purezza:98.17%Colore e forma:White SolidPeso molecolare:347.33RSV-IN-7
CAS:<p>RSV-IN-7 (example 253) is a RSV inhibitor ( EC 50 : < 0.4 μΜ) .</p>Formula:C27H22F3N7O3Colore e forma:SolidPeso molecolare:549.50BAY-3153
CAS:BAY-3153 is a selective CCR1 ( C-C motif chemokine receptor 1 ) antagonist (human IC 50 =3 nM ; rat IC 50 =11 nM ; mice IC 50 =81 nM) .Formula:C25H29Cl2N3O4Colore e forma:SolidPeso molecolare:506.42GNE-2256
CAS:GNE-2256, also known as molecule 19, is an orally active compound that inhibits Interleukin 1 receptor-associated kinase 4 (IRAK4) with a K i of 1.4 nM and hasFormula:C24H27FN6O4Colore e forma:SolidPeso molecolare:482.51TP-030-2
CAS:TP-030-2 is a RIPK1 inhibitor (human K i =0.43 nM ; mouse IC 50 =100 nM) .Formula:C23H21BrN4O3Colore e forma:SolidPeso molecolare:481.34TP-030-1
CAS:TP-030-1, RIPK1 inhibitor: K(i) hRIPK1 at 3.9nM, IC50 mRIPK1 at 4.2μM; targets inflammation, neurodegeneration research.Formula:C23H22N4O3Colore e forma:SolidPeso molecolare:402.45CK2-IN-4
CAS:CK2-IN-4 is a protein kinase (CK2) inhibitor with an IC50 value of 8.6 µM.Formula:C18H11N3O4SPurezza:99.65%Colore e forma:SolidPeso molecolare:365.36IGUANA-1
CAS:<p>IGUANA-1 is a highly efficient and selective ALDH1B1 inhibitor that inhibits the growth of colorectal cancer cells and colorectal cancer cell-derived organoids.</p>Formula:C27H26ClN3O4Purezza:99.08%Colore e forma:SolidPeso molecolare:491.97MSC-1186
CAS:MSC-1186 selectively inhibits SRPKs—IC50: 2.7nM (SRPK1), 81nM (SRPK2), 0.6nM (SRPK3)—for cancer research.Formula:C19H17ClFN7O2SColore e forma:SolidPeso molecolare:461.9TMV-IN-1
CAS:TMV-IN-1: a chalcone inhibits TMV with EC50s of 70.7 and 60.8 μg/mL, applicable in infection and tumor studies.Formula:C28H26O4Colore e forma:SolidPeso molecolare:426.5DHBP dibromide
CAS:DHBP dibromide (1,1'-DI-N-HEPTYL-4,4'-BIPYRIDINIUM DIBRO) is calcium release and a muscle relaxant inhibitor.Formula:C24H38Br2N2Purezza:99.73%Colore e forma:Yellow To Yellow-Green Powder Or FlakesPeso molecolare:514.38CK2-IN-6
CAS:CK2-IN-6: Potent CK2 inhibitor for cancer, inflammation, pain, and immune research.Formula:C19H16ClN7O2Colore e forma:SolidPeso molecolare:409.83BGB-8035
CAS:<p>BGB-8035 is a BTK inhibitor with antitumor activity that inhibits BTK, TEC, and EGFR.BGB-8035 is used in the study of tumors and autoimmune diseases.</p>Formula:C24H31N5O4Purezza:96.74%Colore e forma:SolidPeso molecolare:453.53SZM-1209
CAS:<p>SZM-1209 is a potent and specific RIPK1 inhibitor with oral activity, displaying a dissociation constant (Kd) of 85 nM.</p>Formula:C31H29F5N4O5S2Purezza:98%Colore e forma:SolidPeso molecolare:696.71GLPG3970
CAS:GLPG3970, a pioneering inhibitor of SIK2/SIK3, is utilized in the investigation of inflammation and autoimmune diseases.Formula:C25H27F3N4O4Purezza:99.60% - >99.99%Colore e forma:SolidPeso molecolare:504.5DKFZ-748
CAS:<p>DKFZ-748 is a selective HDAC10 inhibitor and has a dose-dependent growth inhibitory effect on HeLa cells.</p>Formula:C18H23N3O3Purezza:98.10%Colore e forma:SolidPeso molecolare:329.39RGT-068A
CAS:RGT-068A is a potent, selective and oral bioavailable MALT1 inhibitor .Formula:C17H16ClN9O2Colore e forma:SolidPeso molecolare:413.82DHBP
CAS:DHBP (Benzoresorcinol) is an WalKR TCS activator.Formula:C13H10O3Purezza:99.95%Colore e forma:Light-Yellow Solid CrystallinePeso molecolare:214.22Angiotensin (1-7)
CAS:Angiotensin (1-7) (ASP-ARG-VAL-TYR-ILE-HIS-PRO) is a synthetic heptapeptide, inhibits canine ACE activity with vasodilator and antiproliferative activities.Formula:C41H62N12O11Purezza:>99.99%Colore e forma:White Lyophilised SolidPeso molecolare:899I-BET432
I-BET432, a BET inhibitor, blocks BRD4 BD1/BD2 (pIC50: 7.5/7.2), is oral, and targets cancer/inflammation.Formula:C18H21N3O3Colore e forma:SolidPeso molecolare:327.38BLM-IN-2
BLM-IN-2: BLM inhibitor, IC50=0.8 μM; hinders CRC cell growth, invasion, cycle arrest, and death.Formula:C33H38BrFN4OColore e forma:SolidPeso molecolare:605.58TUL01101
CAS:TUL01101, a selective oral JAK1 inhibitor (IC50: 3 nM), also targets JAK2, JAK3, TYK2; for rheumatoid arthritis research.Formula:C22H25F2N5O2Colore e forma:SolidPeso molecolare:429.46BAY-7081
BAY-7081 is a cyanopyridone-based compound that functions as a potent, selective, and orally active PDE9A inhibitor, demonstrating an inhibition concentration (Formula:C19H27ClN4OColore e forma:SolidPeso molecolare:362.9ASPER-29
CAS:ASPER-29, an Asperphenamate analog, inhibits cathepsins L/S with IC50s of 6.03/5.02 μM, useful in cancer migration/invasion research.Formula:C31H29BrN2O5SColore e forma:SolidPeso molecolare:621.54ARS-2102
CAS:ARS-2102 is a potent covalent KRAS G12C inhibitor for use in cancer research .Formula:C28H31ClF2N6O2Colore e forma:SolidPeso molecolare:557.03ENT-C225
CAS:ENT-C225 is a potent TrkB neurotrophin receptor (TrkBR) activator with neuroprotective activity for the study of Alzheimer's disease and Parkinson's disease.Formula:C26H40N4O5Purezza:99.36% - 99.36%Colore e forma:SolidPeso molecolare:488.62FTX-6746
CAS:FTX-6746 is an orally active and selective PPARG reverse inhibitor with anticancer activity. It can be used in research on urothelial carcinoma.Formula:C16H7ClF2N2OPurezza:98.68%Colore e forma:SolidPeso molecolare:316.695'-N-Ethylcarboxamidoadenosine
CAS:NECA, an adenosine receptor agonist, boosts brain extravasation of fluorescein and dextran without affecting the blood-brain barrier.Formula:C12H16N6O4Purezza:98.95% - ≥95%Colore e forma:PowderPeso molecolare:308.29PG-11047
CAS:PG-11047 (CGC-11047) is a polyamine analogue utilized in breast cancer research.Formula:C14H32N4Colore e forma:SolidPeso molecolare:256.43PG-11047 2HCl
PG-11047 2HCl treats genitourinary, immune, genetic, ocular, blood/lymphatic disorders, and aids lymphoma/prostate cancer research.Formula:C14H34Cl2N4Purezza:97.47%Colore e forma:SolidPeso molecolare:329.35Debneyol
CAS:Debneyol exhibits more potent fungicidal activity than validamycin.Formula:C15H26O2Colore e forma:SolidPeso molecolare:238.37Flavipin
CAS:Flavipin: Ahr agonist, alters Ahr genes in T cells/macrophages, disrupts Arid5a, scavenges DPPH (IC50=7.2μM), inhibits α-glucosidase (IC50=33.8μM).Formula:C9H8O5Colore e forma:SolidPeso molecolare:196.16Aviculin
CAS:Aviculin, a lignan glycoside, exhibits anticancer properties by inducing apoptosis in breast cancer cells with an IC50 of 75.47 μM.Formula:C26H34O10Colore e forma:SolidPeso molecolare:506.54JNJ-9350
CAS:<p>JNJ-9350: SMOX inhibitor (IC50 0.01 μM), PAO inhibitor (IC50 0.79 μM), for cancer research.</p>Formula:C25H22N6OColore e forma:SolidPeso molecolare:422.48Immepip
CAS:Immepip, a H3 agonist, has been shown to attenuate cortical histamine release and is utilized in the research of neurological diseases.Formula:C9H15N3Colore e forma:SolidPeso molecolare:165.24SBI-993
CAS:SBI-993 is a potent SBI-477 analog with good pharmacokinetics and enhances insulin signaling by inhibiting MondoA.Formula:C23H24N4O4SColore e forma:SolidPeso molecolare:452.53Diclofensine
CAS:<p>Diclofensine (Ro 8-4650) inhibits the uptake of serotonin, noradrenaline and dopamine.</p>Formula:C17H17Cl2NOPurezza:97.01% - 98.13%Colore e forma:SolidPeso molecolare:322.23MK-4541
CAS:MK-4541: oral, selective AR modulator, blocks 5α-reductase, curbs AR+ prostate cancer growth, effective in mouse model.Formula:C22H31F3N2O3Colore e forma:SolidPeso molecolare:428.49PV-1019
CAS:PV-1019 (NSC 744039), a potent Chk2 inhibitor, has an IC50 of 24 nM and blocks Chk2 autophosphorylation and IR-induced apoptosis.Formula:C18H17N7O3Colore e forma:SolidPeso molecolare:379.37Cadein1
Cadein1, an isoquinolinium derivative, induces G2/M phase delay and caspase-dependent apoptosis in cancer cells lacking functional p53.Formula:C33H48F2INO2Colore e forma:SolidPeso molecolare:655.64EDP-305
CAS:<p>EDP-305, an oral FXR agonist, has EC50s of 34 nM/8 nM in CHO/HEK cells, aids in PBC and NASH research with antifibrotic properties.</p>Formula:C36H58N2O5SColore e forma:SolidPeso molecolare:630.92Miclxin
CAS:Miclxin (DS37262926) is a novel MIC60 inhibitor that induces apoptosis through mitochondrial stress in mutant tumor cells via β-catenin.Miclxin is a potentFormula:C26H27N5O2Purezza:99.17% - 99.99%Colore e forma:SolidPeso molecolare:441.52BiCAPPA
CAS:BiCAPPA, a bivalent antiprion, reduces scrapie-infected prion proteins with 0.32 μM efficiency.Formula:C38H40Cl2N6O2Colore e forma:SolidPeso molecolare:683.67Con B-1
CAS:ConB-1 is a potent and selective ALK inhibitor with low toxicity to normal cells .Formula:C38H52ClN7O6SColore e forma:SolidPeso molecolare:770.38JMX0293
<p>JMX0293, a salicylamide derivative, inhibits STAT3, inducing MDA-MB-231 cell apoptosis with IC50=3.38μM, while sparing MCF-10A (IC50>60μM).</p>Formula:C25H30Cl2N4O7Colore e forma:SolidPeso molecolare:569.43BM212
CAS:BM212 is an antimycobacterial compound.It inhibits the growth of laboratory and clinical isolate M. tuberculosis strains.Formula:C23H25Cl2N3Purezza:99.13%Colore e forma:SolidPeso molecolare:414.37SP-471P
CAS:SP-471P inhibits DENV protease; EC50: DENV1-5.9 μM, DENV2-1.4 μM, DENV3-5.1 μM, DENV4-1.7 μM; CC50 >100 μM; lowers viral RNA synthesis.Formula:C33H26BrN5O2Colore e forma:SolidPeso molecolare:604.5CPT-Se3
CAS:CPT-Se3, a camptothecin derivative, boosts anticancer activity, triggers apoptosis in Hep G2, and is cytotoxic to various cells with IC50 of 2.19-4.7 μM.Formula:C24H20N2O6Se2Purezza:98%Colore e forma:SolidPeso molecolare:590.35CPT-Se4
CAS:CPT-Se4, a seleno-derivative of CPT, effectively kills cancer cells, triggers apoptosis, and is cytotoxic against various cell lines.Formula:C25H24N2O7Se2Purezza:98%Colore e forma:SolidPeso molecolare:622.39
