c-RET
Les inhibiteurs de c-RET ciblent le proto-oncogène RET (Rearranged during Transfection), qui code une tyrosine kinase réceptrice impliquée dans la croissance, la différenciation et la survie cellulaire. L'activation anormale de la signalisation RET peut entraîner une prolifération cellulaire incontrôlée et une résistance à l'apoptose, contribuant au développement de cancers tels que le carcinome médullaire de la thyroïde et le cancer du poumon non à petites cellules. L'inhibition de c-RET peut induire l'apoptose dans les cellules cancéreuses et constitue une approche prometteuse dans la thérapie ciblée du cancer. Chez CymitQuimica, nous offrons une variété d'inhibiteurs de c-RET de haute qualité pour soutenir vos recherches en oncologie, transduction du signal et apoptose.
58 produits trouvés pour "c-RET"
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BT-13
CAS :BT-13 activates RET receptor without GFLs, fostering sensory neuron neurite growth in vitro.Formule :C23H27F4N3O4SDegré de pureté :99.23%Couleur et forme :SolidMasse moléculaire :517.54RET ligand-1
CAS :RETligand-1 is a target protein ligand that specifically interacts with RET and can be utilized in the synthesis of the PROTAC LDD39.Formule :C28H24F2N6O3Couleur et forme :SolidMasse moléculaire :530.525Compound TPX-0046
CAS :Compound TPX-0046 is an inhibitor of RET. Compound TPX-0046 can inhibit the RET autophosphorylation. Compound TPX-0046 can be used for the research of cancer.Formule :C21H21FN6O3Degré de pureté :99.94%Couleur et forme :SoildMasse moléculaire :424.43RET-IN-29
RET-IN-29 (Compound 8W) is a selective RET kinase inhibitor. It demonstrates inhibitory effects on BaF3 cells with the CCDC6-RETV804M mutation, with an IC50 of 0.715 μM. RET-IN-29 shows potential for research in non-small cell lung cancer (NSCLC).Formule :C22H22N6OMasse moléculaire :386.45RET-IN-28
CAS :RET-IN-28 (Compound 16) is an inhibitor of RET (a transmembrane receptor tyrosine kinase). It specifically inhibits the activity of a mutant RET enzyme (RET-V804M) and is utilized in cancer research.Formule :C26H29N9Couleur et forme :SolidMasse moléculaire :467.57RET Ligand-Linker Conjugate-1
RET Ligand-Linker Conjugate-1 consists of a complex formed by a RET ligand and a linker, which can be utilized in the synthesis of QZ2135.Formule :C40H44N10OCouleur et forme :SolidMasse moléculaire :680.84Zeteletinib hemiadipate
CAS :Zeteletinib hemiadipate (BOS-172738; DS-5010) is an oral RET kinase blocker with nanomolar potency and strong anti-tumor properties.Formule :C56H56F6N8O12Couleur et forme :SolidMasse moléculaire :1147.098QZ2135
<p>QZ2135 (compound 20) is a PROTAC degrader that specifically targets RET and exhibits antitumor activity in vivo within a Ba/F3-KIF5B-RET-G810C xenograft mouse model. The compound demonstrates degradation activity with DC50 values of 4.7 nM (WT), 17.2 nM (V804M), and 73.8 nM (G810C) when targeting KIF5B-RET. QZ2135 is composed of the target protein ligand (red part) RETligand-3, the E3 ligase ligand (blue part) Lenalidomide-F, and the PROTAC Linker (black part) 7-Iodohept-1-yne, wherein the target protein ligand combined with the linker forms the conjugate RETLigand-Linker Conjugate-1.</p>Formule :C53H54N12O4Couleur et forme :SolidMasse moléculaire :923.07RET-IN-4
CAS :RET-IN-4: Oral RET inhibitor, IC50 ~1 nM for variants. Selective over JAK2/FLT3. Potent anticancer use.Formule :C27H31FN10O2Couleur et forme :SolidMasse moléculaire :546.611PLM-101
<p>PLM-101 is an anticancer compound orally active against acute myeloid leukemia by targeting FLT3 and RET.</p>Formule :C22H22FN5O2Couleur et forme :SolidMasse moléculaire :407.44RET-IN-26
RET-IN-26 (compound D5) is a kinase inhibitor that selectively targets the RET protein with an IC50 value of 0.33 μM [1].Couleur et forme :Odour SolidAD57 (hydrochloride)
CAS :AD57, a polypharmacological agent, blocks RET kinase (IC50: 2 nM), disrupts related kinases, and hinders cancerous activities like invasion and proliferation.Formule :C22H21ClF3N7ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :491.9YW-N-7 TFA
YW-N-7 (TFA) is a PROTAC designed to target, inhibit, and degrade RET kinase, demonstrating a DC50 of 88 nM. It exhibits antitumor activity in xenograft mouse models driven by KIF5B-RET, making it a valuable compound for cancer research.Formule :C58H63F3N12O9Couleur et forme :SolidMasse moléculaire :1129.19BT44
CAS :BT44, a potent second-gen GDNF mimetic, is a lead for treating neurodegeneration.Formule :C28H27F4N3O4SDegré de pureté :99.87%Couleur et forme :SoildMasse moléculaire :577.59RET ligand-3
RETligand-3 is the ligand for PROTAC QZ2135, which targets RET.Formule :C38H42N10O3Couleur et forme :SolidMasse moléculaire :686.81trans-Pralsetinib
CAS :trans-Pralsetinib (trans-BLU-667) is an inhibitor of rearranged during transfection (RET).Formule :C27H32FN9O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :533.6WHI-P180
CAS :WHI-P180 (Janex 3) is a potent EGFR and Cdk2 inhibitors with IC50 of 4.0 and 1.0 uM, respectively.Formule :C16H15N3O3Degré de pureté :99.21%Couleur et forme :SolidMasse moléculaire :297.31Pyrazoloadenine
CAS :Pyrazoloadenine (4-Aminopyrazolo[3,4-d]pyrimidine) is the inhibitor of human xanthine oxidase.Formule :C5H5N5Degré de pureté :99.02%Couleur et forme :Beige PowderMasse moléculaire :135.13SPP-86
CAS :SPP-86 is an effective and selective cell-permeable inhibitor of RET tyrosine kinase with an IC50 of 8 nM.Formule :C16H15N5Degré de pureté :99.53%Couleur et forme :SolidMasse moléculaire :277.32WHI-P180 hydrochloride
CAS :WHI-P180 (Janex 3) inhibits RET, KDR and EGFR with IC50 values of 5 nM, 66 nM and 4 μM, respectively. WHI-P180 is a multi-kinase inhibitor.Formule :C16H16ClN3O3Couleur et forme :SolidMasse moléculaire :333.77Pralsetinib
CAS :Pralsetinib (Blu667) (BLU-667) is a highly potent, selective RET inhibitor (IC50s: 0.4, 0.3, 0.4, 0.4, and 0.4 nM for WT RET, RET mutants V804L, V804M, M918TFormule :C27H32FN9O2Degré de pureté :97.88% - 99.8%Couleur et forme :SolidMasse moléculaire :533.6AD80
CAS :AD80, a multikinase inhibitor, inhibits RET, RAF, SRCand S6K, with greatly reduced mTOR activity.Formule :C22H19F4N7ODegré de pureté :99.49% - 99.75%Couleur et forme :SolidMasse moléculaire :473.43Treprostinil Sodium
CAS :Treprostinil Sodium (UT-15) is a potent DP1, IP and EP2 agonist (EC50: 0.6/1.9/6.2 nM).Formule :C23H33NaO5Degré de pureté :99.67% - >99.99%Couleur et forme :SolidMasse moléculaire :412.5GSK3179106
CAS :GSK3179106 is RET kinase inhibitor with an IC50 of 0.4 nMFormule :C22H21F4N3O4Degré de pureté :99.8% - 99.90%Couleur et forme :SolidMasse moléculaire :467.41Selpercatinib
CAS :"Selpercatinib (LOXO-292) is a RET tyrosine kinase inhibitor with IC50s of 14.0, 24.1, 530.7 nM for different RET mutations."Formule :C29H31N7O3Degré de pureté :99.89% - >99.99%Couleur et forme :SolidMasse moléculaire :525.6TPX-0046
CAS :<p>TPX-0046 is a RET inhibitor designed to overcome resistance to Selpercatinib and Pralsetinib.</p>Formule :C21H21FN6O3Degré de pureté :99.95%Couleur et forme :SolidMasse moléculaire :424.43RET V804M-IN-1
CAS :RET V804M-IN-1 (RETV804M kinase inhibitor) is a wt-RET -selective RETV804M kinase inhibitors(IC50 = 20 nM).Formule :C19H16N6ODegré de pureté :97.94% - 99.62%Couleur et forme :SolidMasse moléculaire :344.37BBT594
CAS :<p>BBT594 (NVP-BBT594)(NVP-BBT594) is a potent inhibitor of receptor tyrosine kinase RET,Treatment of cancer.</p>Formule :C28H30F3N7O3Degré de pureté :99.57%Couleur et forme :SolidMasse moléculaire :569.58RET-IN-8
CAS :<p>RET-IN-8 is an inhibitor of rearrangement kinase (RET) during transfection and can be used in cancer research.</p>Formule :C27H30N6O3Couleur et forme :SolidMasse moléculaire :486.57RET-IN-16
CAS :RET-IN-16: Selective RET inhibitor, IC50s 3.98-15.05 nM for various RET mutations; anticancer properties.Formule :C31H29F3N8O2Couleur et forme :SolidMasse moléculaire :602.61RET-IN-12
CAS :RET-IN-12 is a RET inhibitor capable of acting on RET(WT) (IC50: 0.3 nM) and RET(V804M) (IC50: 1 nM).Formule :C30H30F3N5O4Couleur et forme :SolidMasse moléculaire :581.59RET-IN-22
CAS :<p>RET-IN-22 (compound 17b) is a potent, selective, and orally active inhibitor of RET, exhibiting IC50 values of 20.9 nM for wild-type RET and 18.3 nM for RET-</p>Formule :C29H31F3N6O4Couleur et forme :SolidMasse moléculaire :584.59RET-IN-15
CAS :RET-IN-15 is an inhibitor of rearrangement kinase (RET) during transfection and can be used in cancer research.Formule :C27H28N8O2Couleur et forme :SolidMasse moléculaire :496.56DUN73423
CAS :<p>DUN73423 (RET-IN-21) is a potent tyrosine kinase (RET) inhibitor with antitumour activity for the study of cancer.</p>Formule :C19H16N6ODegré de pureté :98.09%Couleur et forme :SolidMasse moléculaire :344.37XMD15-44
CAS :XMD15-44, a RET kinase inhibitor, demonstrates potent growth-inhibitory effects on RAT1 cells transformed by RET/C634R and RET/M918T, with IC50 values of 11.5 nM and 8.3 nM, respectively. It effectively inhibits RET kinase activity and signaling in human thyroid cancer cell lines harboring oncogenic RET alleles, thereby reducing cell proliferation.Formule :C29H29F3N4OMasse moléculaire :506.56TRK II-IN-1
CAS :<p>TRK II-IN-1: potent type II TRK inhibitor; IC50s: TRKA (3.3 nM), TRKB (6.4 nM), TRKC (4.3 nM), TRKA G667C (9.4 nM); also targets FLT3, RET, VEGFR2.</p>Formule :C29H31F3N8ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :564.6RET-IN-6
CAS :RET-IN-6 is a potent inhibitor of RET (IC50: 4.57 nM).Formule :C30H29N7Couleur et forme :SolidMasse moléculaire :487.6RET-IN-23
CAS :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.Formule :C28H28FN11Degré de pureté :97.46%Couleur et forme :SolidMasse moléculaire :537.59RET-IN-3
CAS :<p>RET-IN-3 is a RETV804M kinase inhibitor with potential anticancer activity for the study of non-small cell lung cancer.</p>Formule :C18H21N5O2Degré de pureté :99.52%Couleur et forme :SolidMasse moléculaire :339.39RET-IN-13
CAS :RET-IN-13: potent quinoline RET inhibitor; IC50 = 0.5 nM (WT), 0.9 nM (V804M); potential for RET-related tumor/intestinal disease research.Formule :C32H33F4N5O3Couleur et forme :SolidMasse moléculaire :611.63RET-IN-24
CAS :<p>RET-IN-24 (Compound 26) is a selective inhibitor of RET tyrosine kinase, demonstrating antitumor activity [1].</p>Formule :C27H26F2N8OCouleur et forme :SolidMasse moléculaire :516.55Vepafestinib
CAS :<p>Vepafestinib is a RET inhibitor with potential antineoplastic activity[1].</p>Formule :C26H30N6O3Degré de pureté :98.56%Couleur et forme :SolidMasse moléculaire :474.55RET-IN-17
CAS :RET-IN-17 inhibits RET kinase; may help in IBS pain and RET-activated cancers.Formule :C27H28F4N4O4Couleur et forme :SolidMasse moléculaire :548.53NSC194598
CAS :NSC194598 is a p53 DNA-binding inhibitor, demonstrating an in vitro IC50 of 180 nM and an in vivo range of 2-40 μM.Formule :C20H19N3OCouleur et forme :SolidMasse moléculaire :317.38FHND5071
CAS :FHND5071, a potent and selective RET kinase inhibitor, exerts antitumor effects through the inhibition of RET autophosphorylation and may be utilized for tumorFormule :C30H30D3N9OCouleur et forme :SolidMasse moléculaire :538.66RET-IN-5
CAS :RET-IN-5 is a potent inhibitor of RET (IC50: 4.57 nM).Formule :C29H26FN9OCouleur et forme :SolidMasse moléculaire :535.57RET-IN-25
CAS :RET-IN-25 (compound 6b) is an anticancer RET kinase inhibitor that demonstrates efficacy against medullary thyroid carcinoma (MTC), exhibiting half-maximalFormule :C22H17N3O5SCouleur et forme :SolidMasse moléculaire :435.45FLT3/ITD-IN-4
CAS :FLT3/ITD-IN-4 inhibits FLT3-ITD mutations in acute myeloid leukemia (IC50: 2.3 nM).Formule :C25H22N4O5Couleur et forme :SolidMasse moléculaire :458.47WF-47-JS03
<p>WF-47-JS03: RET kinase inhibitor, crosses blood-brain barrier, 500x more selective for KDR, IC50: 1.7 nM in Ba/F3 cells, 5.3 nM in LC-2/ad lung cancer cells.</p>Formule :C30H38N6O2Couleur et forme :SolidMasse moléculaire :514.66RET-IN-1
CAS :RET-IN-1 is a RET kinase inhibitor (IC50s: 1 nM, 7 nM, and 101 nM for RET (WT), RET (V804M) , and RET (G810R), respectively).Formule :C29H31N9O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :553.61
