Apoptose
Os inibidores da apoptose são compostos que previnem ou retardam o processo de morte celular programada, conhecido como apoptose. Esses inibidores são vitais no estudo dos mecanismos de sobrevivência celular e são usados para investigar doenças onde a apoptose é desregulada, como câncer, distúrbios neurodegenerativos e doenças autoimunes. Ao modular a apoptose, esses inibidores podem ajudar no desenvolvimento de terapias destinadas a controlar a morte celular. Na CymitQuimica, oferecemos uma ampla seleção de inibidores da apoptose de alta qualidade para apoiar sua pesquisa em biologia celular, oncologia e áreas relacionadas.
Subcategorias de "Apoptose"
- ASK(6 produtos)
- BCL(11 produtos)
- Caspase(125 produtos)
- FOXO1(3 produtos)
- IAP(66 produtos)
- Mdm2(12 produtos)
- PD-1/PD-L1(125 produtos)
- PDK(9 produtos)
- PERK(25 produtos)
- Serina/treonina quinase(15 produtos)
- Survivina(13 produtos)
- TNF(92 produtos)
- c-RET(51 produtos)
- p53(62 produtos)
Exibir 6 mais subcategorias
Foram encontrados 5593 produtos de "Apoptose"
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NM-3
CAS:<p>NM-3, an oral anti-angiogenic and anti-tumor agent, modulates radiation and blocks VEGF to curb endothelial growth and induce apoptosis.</p>Fórmula:C13H12O6Pureza:99.89%Cor e Forma:SolidPeso molecular:264.23EGFR-IN-11
CAS:<p>EGFR-IN-11 selectively blocks EGFR-tyrosine kinase and promotes apoptosis; targets EGFRL858R/T790M/C797S, IC50=18 nM; halts cell cycle at G0/G1.</p>Fórmula:C29H35N9O2SPureza:99.93%Cor e Forma:SolidPeso molecular:573.71UK-101
CAS:<p>UK-101 is a potent and selective inhibitor of the immunoproteasome LMP2, inhibiting β1i (LMP2), β1c (LMP2), and β5 (LMP2), with IC50s of 104 nM, 15 μM, and 1 μM</p>Fórmula:C25H48N2O5SiPureza:99.08% - 99.25%Cor e Forma:SolidPeso molecular:484.74LQZ-7F
CAS:<p>LQZ-7F is a survivin dimerization inhibitor with anticancer activity.LQZ-7F induces proteasome-dependent survivin degradation and inhibits human tumor growth.</p>Fórmula:C14H7N9O3Pureza:98.64%Cor e Forma:SolidPeso molecular:349.26Necrostatin-5
CAS:<p>Necrostatin-5 (Nec-5) inhibits RIP1 kinase, prevents cell necrosis, and protects Fadd-deficient Jurkat cells with an EC50 of 240 nM.</p>Fórmula:C19H17N3O2S2Pureza:98.03%Cor e Forma:SolidPeso molecular:383.49Ro 90-7501
CAS:<p>Ro 90-7501, an amyloid β42 (Aβ42) protofibril and TPR-dependent PP5 inhibitor, is a novel cervical cancer cell radiosensitizer that inhibits HCMV.</p>Fórmula:C20H16N6Pureza:97.21% - 99.72%Cor e Forma:SolidPeso molecular:340.38GS-9191
CAS:<p>GS-9191 is a potent inhibitor of DNA polymerase alpha and ß , a prodrug of the novel nucleoside analogue 9-(2-phosphonomethoxyethyl)guanine (PMEG) , which</p>Fórmula:C37H51N8O6PPureza:98.01 - 99.28%Cor e Forma:SolidPeso molecular:734.82Alethine
CAS:<p>Alethine is a small antitumor compound used to treat cancers and infections, boosting T-cell cytotoxicity by raising TNFα.</p>Fórmula:C10H22N4O2S2Pureza:98.83%Cor e Forma:SolidPeso molecular:294.44p53-MDM2-IN-1
CAS:<p>p53-MDM2-IN-1 (Example 30), an inhibitor targeting the p53-MDM2/X protein interaction, exhibits a K i value of 23.35 µM.</p>Fórmula:C23H20ClN3O3Pureza:99.98%Cor e Forma:SoildPeso molecular:421.88iCRT-5
CAS:<p>iCRT-5 is a potent inhibitor of the Wnt pathway. iCRT-5 has antiproliferative activity and can be used in the study of multiple myeloma.</p>Fórmula:C16H17NO5S2Pureza:99.68%Cor e Forma:SolidPeso molecular:367.44Droloxifene
CAS:<p>Droloxifene, a tamoxifen derivative and oral SERM, induces p53 and apoptosis; Fluroxifene protects bone, blocks estrogen and implantation.</p>Fórmula:C26H29NO2Pureza:99.86% - 99.97%Cor e Forma:Solid PowderPeso molecular:387.51STAT3-IN-13
CAS:<p>STAT3-IN-13 is a STAT3 inhibitor with antiproliferative activity that induces apoptosis and can be used to study breast and liver cancer.</p>Fórmula:C21H20N6O3SPureza:98.89%Cor e Forma:SolidPeso molecular:436.49AMG PERK 44
CAS:<p>AMG PERK 44 is a PERK inhibitor that induces autophagy.AMG PERK 44 inhibits GCN2 and B-Raf and can be used in cancer research.</p>Fórmula:C34H29ClN4O2Pureza:98.8% - 99.81%Cor e Forma:SolidPeso molecular:561.07HTH-01-091
CAS:<p>HTH-01-091 is a potent and selective maternal embryonic leucine zipper kinase (MELK) inhibitor (IC50: 10.5 nM).HTH-01-091 inhibits PIM1/2/3, RIPK2, DYRK3,</p>Fórmula:C26H28Cl2N4O2Pureza:98.4%Cor e Forma:SolidPeso molecular:499.43R306465
CAS:<p>R306465 (JNJ-16241199) is an HDAC 1 inhibitor with broad-spectrum anti-tumor activity, inducing apoptosis, and can be used to study solid tumors.</p>Fórmula:C19H19N5O4SPureza:98.46% - 99.54%Cor e Forma:SolidPeso molecular:413.45Mepazine
CAS:<p>Mepazine, a MALT1 inhibitor, blocks GSTMALT1 (IC50: 0.83μM) and GSTMALT1 325-760 (IC50: 0.42μM), promoting apoptosis and reducing cell viability.</p>Fórmula:C19H22N2SPureza:99.88% - 99.92%Cor e Forma:SolidPeso molecular:310.46Tubulin inhibitor 11
CAS:<p>Potent, oral Tubulin inhibitor 11 hinders polymerization, targets Colchicine site, induces mitotic block, and apoptosis.</p>Fórmula:C22H23N3O3SPureza:98.32%Cor e Forma:SoildPeso molecular:409.5MBM-55
CAS:<p>MBM-55 is an effective inhibitor of NIMA related kinase 2 (NEK2) with an IC50 of 1 nM.</p>Fórmula:C28H27FN6O2Pureza:99.83%Cor e Forma:SolidPeso molecular:498.55LDCA
CAS:<p>LDCA inhibits LDH-A, disrupts mitochondrial function, induces apoptosis in cancer cells, and is non-toxic.</p>Fórmula:C8H5Cl3FNOPureza:98.99%Cor e Forma:SolidPeso molecular:256.49NSC49652
CAS:<p>NSC49652 triggers apoptotic cell death dependent on p75NTR and JNK activity in neurons and melanoma cells, and inhibits tumor growth in a melanoma mouse model.</p>Fórmula:C14H11NO2Pureza:98.98%Cor e Forma:SolidPeso molecular:225.24SCFSkp2-IN-2
CAS:<p>SCFSkp2-IN-2, a Skp2 inhibitor, exhibits a dissociation constant (K_D) of 28.77 μM.</p>Fórmula:C17H20N4O2Pureza:99.86%Cor e Forma:SolidPeso molecular:312.37UCB-5307
CAS:<p>UCB-5307 inhibits TNFR1, binds TNFα with 9 nM KD, shows slow kinetics (KD=6 nM), and penetrates hTNF/hTNFR1 complexes.</p>Fórmula:C22H21N3OPureza:98.76%Cor e Forma:SolidPeso molecular:343.42AQ4
CAS:<p>AQ4 is a topoisomerase II inhibitor and DNA-inserting agent that inhibits proliferation and induces apoptosis in two cell lines.</p>Fórmula:C22H28N4O4Pureza:96.28% - 97.15%Cor e Forma:SolidPeso molecular:412.48Gallium maltolate
CAS:<p>Gallium maltolate is a ribonucleoside-diphosphate reductase inhibitor.</p>Fórmula:C18H15GaO9Pureza:99.61% - 99.67%Cor e Forma:SolidPeso molecular:445.03RIPK3-IN-1
CAS:<p>RIPK3-IN-1 is a RIPK3 inhibitor (IC50: 9.1 nM) that inhibits c-Met kinase, RIPK1, and RIPK2 activity and can be used to study apoptosis.</p>Fórmula:C29H25FN4O4Pureza:98.27%Cor e Forma:SolidPeso molecular:512.53Minodronic acid
CAS:Minodronic acid (YM-529) is a P2X2/3 antagonist with anticancer properties, inhibiting cell growth and metastasis, and used in osteoporosis research.Fórmula:C9H12N2O7P2Pureza:98.02%Cor e Forma:SolidPeso molecular:322.15Sarmustine
CAS:<p>SarCNU is an alkylating anticancer drug targeting prostate cancer through p53 pathways and selects P140K MGMT-transduced CD34(+) cells.</p>Fórmula:C6H11ClN4O3Pureza:98.29% - 99.71%Cor e Forma:SolidPeso molecular:222.63UC-112
CAS:<p>UC-112 is a novel potent IAP inhibitor and potently inhibits cell growth in two human melanoma and two human prostate cancer cell lines (IC50=0.7-3.4 uM).</p>Fórmula:C22H24N2O2Pureza:99.54%Cor e Forma:SolidPeso molecular:348.44Apostatin-1
CAS:<p>Apostatin-1 (Apt-1) is a novel TRADD inhibitor. Apostatin-1 can bind to a pocket on the N-terminal TRAF2 binding domain of TRADD.</p>Fórmula:C19H27N3OSPureza:99.31%Cor e Forma:SolidPeso molecular:345.5AOH1160
CAS:<p>AOH1160 is an inhibitor of proliferating cell nuclear antigen (PCNA).</p>Fórmula:C25H20N2O3Pureza:98.46% - 99.52%Cor e Forma:SolidPeso molecular:396.44Dasatinib hydrochloride
CAS:<p>Dasatinib hydrochloride is an oral Src/Bcr-Abl inhibitor with potent antitumor effects, Ki values of 16 pM (Src) and 30 pM (Bcr-Abl).</p>Fórmula:C22H27Cl2N7O2SPureza:99.88% - 99.98%Cor e Forma:SolidPeso molecular:524.47XX-650-23
CAS:<p>XX-650-23 is a CREB inhibitor that induces apoptosis and cell cycle arrest in AML cells and can be used to study acute myeloid leukemia (AML).</p>Fórmula:C18H12N2O2Pureza:97.01%Cor e Forma:SolidPeso molecular:288.3CSN5i-3
CAS:<p>CSN5i-3 is a potent, selective, and orally available inhibitor of the proteolytic subunit of the CSN complex, CSN5, as an anticancer agent.Cost-effective and quality-assured.</p>Fórmula:C28H29F2N5O2Pureza:99.56% - >99.99%Cor e Forma:SolidPeso molecular:505.56FA16
<p>FA16 is a selective, metabolically stable ferroptosis inducer with an IC50 value of 1.26 μM.FA16 is a derivative of 2-(trifluoromethyl)benzimidazole.FA16</p>Fórmula:C22H27F3N4O2SPureza:99.44%Cor e Forma:SolidPeso molecular:468.54P505-15 Acetate
CAS:<p>P505-15 Acetate inhibits spleen tyrosine kinase, reduces immune response and inflammation, and lowers arthritis severity.</p>Fórmula:C21H27N9O3Pureza:99.99%Cor e Forma:SolidPeso molecular:453.5RO-5963
CAS:<p>RO-5963 is a dual inhibitor of p53-MDM2 and p53-MDMX (IC50s: ~17 nM and ~24 nM, respectively).</p>Fórmula:C24H21ClF2N4O5Pureza:99.28%Cor e Forma:SolidPeso molecular:518.9Vamotinib
CAS:<p>Vamotinib (PF-114) is a tyrosine kinase inhibitor with antiproliferative and antitumor activity.Vamotinib is used in the study of Alzheimer's disease.</p>Fórmula:C29H27F3N6OPureza:99.64%Cor e Forma:SolidPeso molecular:532.56RS1-PDK1 inhibitor
CAS:<p>RS1-PDK1 inhibitor (RS 1) is a selective inhibitor of the protein kinase PDK1 that can be used to treat and prevent disease or disorders.</p>Fórmula:C15H9ClN2O2S3Pureza:98.12%Cor e Forma:SolidPeso molecular:380.89K-8012
CAS:<p>K-8012 is a modulator of the N-terminally truncated RXRα and improves anticancer activities in an RXRα-dependent manner.</p>Fórmula:C23H23FN4Pureza:99.72%Cor e Forma:SolidPeso molecular:374.45DCG066
CAS:<p>DCG066 is an inhibitor of lysine methyltransferase G9a with anticancer activity and may be used in the study of leukemia.</p>Fórmula:C30H31F6N3O2Pureza:98.26% - 98.38%Cor e Forma:SolidPeso molecular:579.58GCN2-IN-1
CAS:<p>GCN2-IN-1 (A-92) is an effective GCN2 inhibitor and can be used in research on the treatment of cancer as a chemotherapeutic agent.</p>Fórmula:C19H18N10OPureza:99.49% - 99.64%Cor e Forma:SolidPeso molecular:402.41Triparanol
CAS:<p>Triparanol (NSC-65345) interferes with posttranslational modification of Hedgehog signaling molecules as well as the sterol sensing domain of its receptor PTCH1</p>Fórmula:C27H32ClNO2Pureza:99.72%Cor e Forma:SolidPeso molecular:438Mitazalimab
CAS:<p>Mitazalimab (ADC-1013/JNJ-64457107) is a CD40 agonist that stimulates T cells to attack tumors and remodels the tumor microenvironment.</p>Pureza:95.1% (SDS-PAGE); 98.7% (SEC-HPLC) - 95.1% (SDS-PAGE); 98.7% (SEC-HPLC)Cor e Forma:LiquidOR-1896
CAS:<p>OR-1896 is a PDE III inhibitor, a vasodilator with partial anti-inflammatory properties, and can be used to study heart failure and vascular dysfunction.</p>Fórmula:C13H15N3O2Pureza:99.33%Cor e Forma:SolidPeso molecular:245.28CUDC-427
CAS:<p>CUDC-427 (GDC-0917) is an orally bioactive and pan antagonist of inhibitor of apoptosis proteins(IAPs). CUDC-427 can be used in research on cancers.</p>Fórmula:C29H36N6O4SPureza:99.92%Cor e Forma:SolidPeso molecular:564.7F16
CAS:<p>F16 ((E)-4-(3-indolylvinyl)-N-methylpyridinium iodide) inhibits the growth of neu-overexpressing cells and the proliferation of mammary epithelial.</p>Fórmula:C16H15IN2Pureza:99.89%Cor e Forma:SolidPeso molecular:362.21Etomoxir
CAS:<p>Etomoxir is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a) (IC50=5-20 nM), inhibits fatty acid oxidation. High-Quality, Low-Cost!</p>Fórmula:C17H23ClO4Pureza:98% - 99.39%Cor e Forma:SolidPeso molecular:326.82CMLD-2
CAS:<p>CMLD-2 is a HuR-ARE inhibitor (Ki: 350 nM) that promotes apoptosis, has antitumor properties, and reduces thyroid cancer cell viability.</p>Fórmula:C31H31NO6Pureza:99.99%Cor e Forma:SolidPeso molecular:513.58NLRP3/AIM2-IN-3
CAS:<p>NLRP3/AIM2-IN-3 selectively blocks NLRP3/AIM2 inflammasomes; IC50 for cell lysis is 0.077 μM, disrupting ASC oligomerization.</p>Fórmula:C16H14N2O2Pureza:97.04%Cor e Forma:SolidPeso molecular:266.29Lanperisone HCl
CAS:<p>Lanperisone (NK433) is a potent, long-lasting muscle relaxant that inhibits spinal reflexes via noradrenergic system suppression.</p>Fórmula:C15H19ClF3NOPureza:98.67% - >99.99%Cor e Forma:SolidPeso molecular:321.77PARP/PI3K-IN-1
CAS:<p>PARP/PI3K-IN-1 is a PARP and PI3K dual inhibitor with anticancer and antiproliferative activities for the study of breast, pancreatic and lung cancers.</p>Fórmula:C33H28F4N8O3Pureza:99.59%Cor e Forma:SolidPeso molecular:660.62Cot inhibitor-1
CAS:<p>Cot inhibitor-1 selectively blocks Tpl2 kinase, reducing TNF-alpha in blood (IC50: 5.7 nM). It may treat arthritis, IBD, and certain cancers.</p>Fórmula:C27H27Cl2FN8Pureza:98.59%Cor e Forma:SolidPeso molecular:553.46cRIPGBM chloride
CAS:<p>cRIPGBM chloride is a pro-apoptotic derivative found in GBM cancer stem cells with anti-tumor activity, inducing caspase-1-dependent apoptosis.</p>Fórmula:C26H20ClFN2O2Pureza:99.75%Cor e Forma:SolidPeso molecular:446.9VAS 3947
CAS:<p>VAS 3947: NOX inhibitor, induces platelet apoptosis via UPR, not linked to NOX inhibition.</p>Fórmula:C14H10N6OSPureza:98.44%Cor e Forma:SolidPeso molecular:310.33Tubulin inhibitor 32
CAS:<p>Tubulin inhibitor 32 is a microtubule inhibitor with antiproliferative and antitumor activity that induces apoptosis and cell cycle arrest in the G2/M phase.</p>Fórmula:C18H19N3O3Pureza:99.92%Cor e Forma:SolidPeso molecular:325.36Ro 08-2750
CAS:<p>Ro 08-2750: A non-peptide NGF inhibitor binding NGF (~1 µM IC50) & selectively inhibits p75NTR over TRKA and MSI RNA-binding (2.7 µM IC50).</p>Fórmula:C13H10N4O3Pureza:98.795%Cor e Forma:SolidPeso molecular:270.24Prinomastat
CAS:<p>Prinomastat: orally active, crosses blood-brain barrier, inhibits MMP-1/2/3/9, Ki/IC50s: 0.05-0.3/5.0-79 nM, antitumor.</p>Fórmula:C18H21N3O5S2Pureza:99.23%Cor e Forma:SolidPeso molecular:423.51C6 Ceramide
CAS:<p>C6 Ceramide (N-hexanoylsphingosine) is an activator of the ceramide pathway that arrests cells in the G0/G1 phase by activating ERK.</p>Fórmula:C24H47NO3Pureza:99.67%Cor e Forma:SolidPeso molecular:397.63SYM 2081
CAS:<p>SYM 2081: Kainate receptor agonist, IC50 of 35 nM, depolarizes muscle, lowers EPSP amplitude.</p>Fórmula:C6H11NO4Pureza:99.59%Cor e Forma:SolidPeso molecular:161.16TL4-12
CAS:<p>TL4-12 is a MAP4K2 (GCK) inhibitor that inhibits IL-1 and TGFβ-induced p38 MAPK phosphorylation in vitro.</p>Fórmula:C25H27F3N6O2Pureza:98.38%Cor e Forma:SolidPeso molecular:500.52N6-Cyclopentyladenosine
CAS:<p>N6-Cyclopentyladenosine (CPA) is a selective agonist of the adenosine A1 receptor and can be used to mimic the action of the adenosine A1 receptor, with Ki's of</p>Fórmula:C15H21N5O4Pureza:99.84%Cor e Forma:SolidPeso molecular:335.36Epristeride
CAS:<p>Epristeride (ONO-9302) is a steroidal 5-alpha-reductase isoform 2 inhibitor that inhibits SR isoform 2. Epristeride reduces prostate size.</p>Fórmula:C25H37NO3Pureza:98.12% - >99.99%Cor e Forma:SolidPeso molecular:399.57Bomedemstat ditosylate
CAS:<p>Bomedemstat (IMG-7289) is an LSD1 inhibitor for acute myeloid leukemia, MDS, and Myelofibrosis; induces apoptosis by regulating p53, PUMA, and BCLXL.</p>Fórmula:C42H50FN7O8S2Pureza:99.05%Cor e Forma:SolidPeso molecular:864.02Imipramine
CAS:<p>Imipramine (Dimipressin) is a Fascin1 inhibitor with antitumor activity and induces apoptosis.</p>Fórmula:C19H24N2Pureza:99.4%Cor e Forma:White To Off-White /Hydrochloride/ SolidPeso molecular:280.41DX3-213B
CAS:<p>DX3-213B is a potent, orally active inhibitor of oxidative phosphorylation (OXPHOS) complex I with an IC50 of 3.6 nM.</p>Fórmula:C20H28F2N2O5S2Pureza:99.85%Cor e Forma:SolidPeso molecular:478.57HBED
CAS:<p>HBED (CHELII) is an iron chelator and can be used in research on the treatment of chronic iron overload and acute iron poisoning.</p>Fórmula:C20H24N2O6Pureza:97.35% - 98.58%Cor e Forma:SolidPeso molecular:388.41BCL6-IN-7
CAS:<p>BCL6-IN-7 (BCL6 inhibitor-7) is a BCL6 corepressor-interaction inhibitor with potential antitumor activity, used in lymphoma research.</p>Fórmula:C18H15ClN6OPureza:99.03%Cor e Forma:SolidPeso molecular:366.8SB 699551 dihydrochloride
CAS:<p>SB 699551 dihydrochloride is a 5-ht5a receptor antagonist.</p>Fórmula:C34H47Cl2N3OPureza:99.83%Cor e Forma:SolidPeso molecular:584.66SLMP53-1
CAS:<p>SLMP53-1 is a p53 activator with anti-tumor activity, activates reprogramming of glucose metabolism, and interferes with angiogenesis and migration</p>Fórmula:C20H18N2O2Pureza:99.64%Cor e Forma:SolidPeso molecular:318.37Brigimadlin
CAS:<p>Brigimadlin (BI 907828) is an orally active and highly potent antagonist of the E3 ubiquitin-protein ligase MDM2-p53 with antitumor activity.</p>Fórmula:C31H25Cl2FN4O3Pureza:98.17%Cor e Forma:SolidPeso molecular:591.46MJN68390
CAS:<p>MJN68390 has an apparent IC50 value of 15 μM against CASP8 and shows no activity against CASP10.</p>Fórmula:C24H28ClN3O3Pureza:98.86%Cor e Forma:SolidPeso molecular:441.95TNIK-IN-3
CAS:<p>TNIK-IN-3 is a highly potent and orally active inhibitor of Traf2- and Nck-interacting protein kinase (TNIK).</p>Fórmula:C23H18FN3O2Pureza:98.39%Cor e Forma:SolidPeso molecular:387.41GSK2593074A
CAS:<p>GSK2593074A (GSK'074) is a programmed necrosis inhibitor that displays inhibitory effects on RIP1 and RIP3.</p>Fórmula:C27H23N5OSPureza:99.76%Cor e Forma:SolidPeso molecular:465.57Deferitazole
CAS:<p>Deferitazole (FBS 0701) is a novel and orally active, selective and high affinity iron chelator.</p>Fórmula:C18H25NO7SPureza:99.48%Cor e Forma:SolidPeso molecular:399.46Antifolate C2
CAS:<p>Antifolate C2 (AGF 154) inhibits tumor growth with 0.14 nM IC, useful in cancer/autoimmune research.</p>Fórmula:C19H21N5O6SPureza:99.57%Cor e Forma:SolidPeso molecular:447.46UNC0321
CAS:<p>UNC0321 is an effective inhibitor of histone methyltransferase G9a with a Ki of 63 pM and with IC50s 9 nM and 6 nM in ECSD and CLOT assays.</p>Fórmula:C27H45N7O3Pureza:99.80%Cor e Forma:SolidPeso molecular:515.69RET-IN-23
CAS:<p>RET-IN-23 is an orally available and highly potent RET inhibitor with significant antitumor activity for the study of non-small cell lung cancer.</p>Fórmula:C28H28FN11Pureza:97.46%Cor e Forma:SolidPeso molecular:537.59DK419
CAS:<p>DK419 is an orally active inhibitor of Wnt/β-catenin signaling, with an IC50 of 0.19 μM.</p>Fórmula:C16H8ClF6N3OPureza:99.63%Cor e Forma:SolidPeso molecular:407.7Tiomolibdate diammonium
CAS:<p>Tiomolibdate diammonium (NSC-286644) blocks SOD1 and COX, acting as an antiangiogenic and antitumor agent.</p>Fórmula:H8MoN2S4Pureza:98%Cor e Forma:Brown To Black Iridescent Crystalline PowderPeso molecular:260.28H2L5186303
CAS:<p>H2L5186303 is an LPA2 antagonist and can be used in studies about asthma treatment.</p>Fórmula:C26H20N2O8Pureza:98.19%Cor e Forma:SolidPeso molecular:488.45TAI-1
CAS:<p>TAI-1 is a potent and specific Hec1 inhibitor, which disrupts Hec1-Nek2 protein interaction.</p>Fórmula:C24H21N3O3SPureza:99.58%Cor e Forma:SolidPeso molecular:431.51D609
CAS:<p>D609 (Tricyclodecan-9-yl-Xanthogenate) has antiviral and antiproliferative activities.D609 acts through competitive inhibition of PC, PC-P and SMS.</p>Fórmula:C11H15KOS2Pureza:97.67% - 99.56%Cor e Forma:Off-White PowderPeso molecular:266.46EM-12
CAS:<p>EM-12, a Thalidomide analogue, is more active, stable, and boosts rat colon cancer studies.</p>Fórmula:C13H12N2O3Pureza:99.34%Cor e Forma:SolidPeso molecular:244.25Ro24-7429
CAS:<p>Ro24-7429: oral HIV-1 Tat antagonist, RUNX1 inhibitor with anti-HIV, antifibrotic, and anti-inflammatory properties.</p>Fórmula:C14H13ClN4Pureza:99.29% - 99.85%Cor e Forma:SolidPeso molecular:272.73CBS9106
CAS:<p>CBS9106 (SL-801) is a CRM1 inhibitor with CRM1-degrading and anti-tumor activity that inhibits CRM1-dependent nuclear export.</p>Fórmula:C18H21ClF3N3O3Pureza:98.98%Cor e Forma:SolidPeso molecular:419.83GSK854
CAS:<p>GSK854 is a selective TNNI3K inhibitor reducing heart damage and stress post-infarction in mice.</p>Fórmula:C18H19ClN6O4S2Pureza:98.79%Cor e Forma:SolidPeso molecular:482.96TC-DAPK 6
CAS:<p>TC-DAPK 6 is an ATP-competitive inhibitor of Death-associated protein kinase (DAPK) with IC50s of 69 and 225 nM for DAPK1 and DAPK3.</p>Fórmula:C17H12N2O2Pureza:98.73%Cor e Forma:SolidPeso molecular:276.29eIF4A3-IN-1
CAS:<p>eIF4A3-IN-1 is an inhibitor of eukaryotic initiation factor 4A3 (eIF4A3). eIF4A3-IN-1 inhibits cytosolic nonsense-mediated RNA decay at high concentrations.</p>Fórmula:C29H23BrClN5O2Pureza:99.49% - 99.89%Cor e Forma:SolidPeso molecular:588.88EB1
CAS:<p>EB1 is an MNK kinase inhibitor that inhibits cancer cell growth, promotes apoptosis, and inhibits eIF4E phosphorylation.</p>Fórmula:C18H14N4Pureza:99.82%Cor e Forma:SolidPeso molecular:286.331G244
CAS:<p>1G244 is an inhibitor of DPP8/9 with antiatherosclerotic and antimyeloma properties.</p>Fórmula:C29H30F2N4O2Pureza:99.14%Cor e Forma:SolidPeso molecular:504.57Sabizabulin
CAS:<p>Sabizabulin (ABI-231) is a potent, orally bioavailable α- and β-tubulin inhibitor.Cost-effective and quality-assured.</p>Fórmula:C21H19N3O4Pureza:98.10% - 99.79%Cor e Forma:SolidPeso molecular:377.39AZA1
CAS:<p>AZA1 (Rac1/Cdc42-IN-1) is a potent dual inhibitor of Rac1 and Cdc42.</p>Fórmula:C22H20N6Pureza:99.75%Cor e Forma:SolidPeso molecular:368.43BC 11 hydrobromide
CAS:<p>The compound is a selective urokinase inhibitor (IC50 = 8.2 μM). It also inhibits clot lysis with no effect on clot formation.</p>Fórmula:C8H12BBrN2O2SPureza:98.07%Cor e Forma:SolidPeso molecular:290.97CDK9-IN-7
CAS:<p>CDK9-IN-7: selective, oral CDK9/cyclin T inhibitor with 11 nM IC50, stronger than CDK4/6.</p>Fórmula:C29H37N7O2SPureza:98.08%Cor e Forma:SolidPeso molecular:547.71W146
CAS:<p>W146 is an S1PR1 antagonist that induces a significant but transient decrease in blood lymphocytes in mice.</p>Fórmula:C16H27N2O4PPureza:99.37%Cor e Forma:SolidPeso molecular:342.37Exisulind
CAS:<p>Exisulind (CP248) triggers apoptosis via PKG activation, shows antitumor effects, and inhibits growth in various rodent cancer models.</p>Fórmula:C20H17FO4SPureza:97.94%Cor e Forma:SolidPeso molecular:372.41Cipepofol
CAS:<p>HSK3486 is similar to propofol and is a general anesthetic, which may have therapeutic potential in insomnia, migraine, anxiety, analgesia, and other aspects.</p>Fórmula:C14H20OPureza:99.77%Cor e Forma:SolidPeso molecular:204.31Perphenazine dihydrochloride
CAS:<p>Perphenazine dihydrochloride: Oral dopamine, histamine-1 antagonist; targets D2, D3, 5-HT2A, Alpha-1A; may treat psychiatric disorders, cancer.</p>Fórmula:C21H28Cl3N3OSPureza:99.67%Cor e Forma:SolidPeso molecular:476.89SPD304 dihydrochloride
CAS:<p>SPD304 dihydrochloride is a selective inhibitor of TNF-α with an IC50 of 22 µM. SPD304 dihydrochloride promotes dissociation of TNF trimers.</p>Fórmula:C32H34Cl2F3N3O2Pureza:99.25%Cor e Forma:SolidPeso molecular:620.53A09-003
CAS:<p>A09-003 Inhibits the proliferation of leukemia cell lines and inhibits the increase of leukemia sequence-1 protein in HI bone marrow cells.</p>Fórmula:C23H26N4OPureza:99.61%Cor e Forma:SolidPeso molecular:374.48
