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Search Results for " cd135 "

Targets

54

Compounds

6

Recombinant Proteins

Cat No. Product Name Synonyms Targets
T2340 AC1NS4RE Tyrosinase
It is a tyrosine kinase inhibitor.
T1938 FLT3-IN-2 FLT
FLT3-IN-2 is an FLT3 inhibitor (IC50<1 μM).
T4428 CCT241736 FLT , Aurora Kinase
CCT241736 is an orally bioavailable dual FLT3/Aurora kinase inhibitor that also inhibits clinically relevant FLT3-resistant mutants including FLT3-ITD and FLT3, CCT241736, an advanced analog of CCT137690, is a preclinica...
T11298 FLT3-IN-3 FLT
FLT3-IN-3 is an effective FLT3 inhibitor, and the IC50s of FLT3 WT and FLT3 D835Y are 13 and 8 nM, respectively.
T2272 BPR1J-097 BPR1J097 FLT
BPR1J-097) is a novel FLT-3 inhibitor(IC50: 11±7 nM) with promising in vivo anti-tumor activities. It also inhibits FLT-3 D835Y (IC50: 3 nM).
T15335 FN-1501 FLT , CDK
FN-1501 is a potent FLT3 and CDK inhibitor (IC50s: 2.47, 0.85, 1.96, and 0.28 nM for CDK2/cyclin A, CDK4/cyclin D1, CDK6/cyclin D1 and FLT3, respectively). FN-1501 also has anticancer activity.
T6756 AMG 925 FLT , CDK
AMG 925 is a potent and orally bioavailable dual FLT3/CDK4 inhibitor with IC50 of 1 nM and 3 nM, respectively.
T6138 TCS 359 FLT3 Inhibitor FLT
TCS 359 (FLT3 Inhibitor) is a potent FLT3 inhibitor with IC50 of 42 nM.
T3065 TG101209 Apoptosis , FLT , c-RET , JAK , Autophagy
TG101209 is a selective JAK2 inhibitor with IC50 of 6 nM.
T7673 ATH686 ATH 686 Apoptosis , FLT
ATH686 is an potent and selective Inhibitor of FLT3.
T9473 4SC-203 FLT
4SC-203 is a multikinase inhibitor with potential antineoplastic activity. 4SC-203 selectively inhibits FMS-related tyrosine kinase 3 (FLT3/STK1), FLT3 mutated forms, and vascular endothelial growth factor receptors (VEG...
T6020 Pacritinib SB1518 FLT , Tyrosine Kinases , JAK
Pacritinib (SB1518) (SB1518) is an effective and specific inhibitor of JAK2 and FLT3 (IC50: 23/22 nM, in cell-free assays).
T8317 5'-Fluoroindirubinoxime 5'-FIO FLT
5'-Fluoroindirubinoxime (5'-FIO) is a potent FLT3 inhibitor( IC50 : 15 nM).
TQ0235 AC710 FLT , PDGFR , c-Kit
AC710 is a potent PDGFR inhibitor (Kds: 0.6, 1, 1.57, 1.3, 1 nM for FLT3, KIT, CSF1R, PDGFRα and PDGFRβ).
T6115 Fostamatinib R788 FLT , Syk , Monoamine Transporter , Adenosine Receptor
Fostamatinib (R788)(IC50 of 41 nM), which is a prodrug of the active metabolite R406, is a Syk inhibitor. It does not work on Lyn.
T16144 MRX-2843 UNC2371 Others , FLT
MRX-2843 (UNC2371) is a potent and orally active inhibitor of MERTK and FLT3(IC50s of 1.3 nM and 0.64 nM, respectively).
T2341 KW-2449 KW2449 Apoptosis , FGFR , FLT , JAK , Bcr-Abl , Src , c-Kit , Aurora Kinase
KW-2449 is a multiple-targeted inhibitor, mostly for Flt3 (IC50: 6.6 nM), modestly effective to Bcr-Abl, FGFR1, and Aurora A; little inhibitory on PDGFRβ, IGF-1R, EGFR.
T6350 CHIR-124 CHIR124,CHIR 124 Apoptosis , GSK-3 , FLT , Chk , PDGFR , Src
CHIR-124 is an effective Chk1 inhibitor (IC50: 0.3 nM). It has 2, 000-fold selectivity against Chk2, 500- to 5, 000-fold less activity against Cdc2 and CDK2/4.
T2620 G-749 G749 Apoptosis , FLT , c-RET , TAM Receptor , Aurora Kinase
G-749, a new-type FLT3 inhibitor, exhibits effective and sustained inhibition of the FLT3 wild type and mutants.
T3455 Merestinib LY2801653 Discoidin Domain Receptor (DDR) , FLT , c-Met/HGFR , ROS , ROS Kinase
Merestinib (LY2801653) is an orally available, small molecule inhibitor of the proto-oncogene c-Met (Ki: 2 nM) with potential antineoplastic activity. Merestinib electively binds to c-Met, thereby inhibiting c-Met phosph...
T38562 AKN-028 FLT
AKN-028 is an orally active and potent FLT3 tyrosine kinase inhibitor ( IC 50 = 6 nM). AKN-028 causes dose-dependent inhibition of FLT3 autophosphorylation.
T2640 Rebastinib DCC2036,DCC 2036,DCC-2036 Apoptosis , FLT , Bcr-Abl , Src
DCC-2036 (Rebastinib (DCC-2036)) is a conformational control Bcr-Abl inhibitor for Abl1(WT, IC50: 0.8 nM) and Abl1(T315I, IC50: 4 nM), also inhibits LYN, SRC, HCK, FGR, FLT3, KDR, and Tie-2, and low activity to c-Kit. Re...
T6174 R406 R-406 besylate Apoptosis , FLT , Syk
R406 (R-406 besylate) is an effective Syk inhibitor (IC50: 41 nM) and shows no effects on Lyn.
T7007 UNC2025 mrx-6313,UNC-2025,UNC 2025 FLT , TAM Receptor
UNC2025 (mrx-6313)(IC50 of 0.74 nM and 0.8 nM) is a potent and orally bioavailable dual MER/FLT3 inhibitor. UNC-2025 is about 20-fold selectivity higher than Axl and Tyro3.
T4409 Gilteritinib ASP2215 FLT , TAM Receptor , c-Kit
Gilteritinib (ASP2215) is a potent inhibitor at the FMS-related tyrosine kinase 3 (FLT3) and AXL tyrosine kinase receptors (IC50 = 0.29 nM and <1 nM, respectively). In preClinicalal studies, gilteritinib showed strong an...
T2638 Gandotinib LY2784544 VEGFR , FGFR , FLT , JAK
LY2784544(Gandotinib (LY2784544)) is a potent JAK2 inhibitor (IC50: 3 nM), effective in JAK2V617F(Ki: 0.245 nM). The selectivity is higher 8- and 20-fold than JAK1 and JAK3.
T2054 Altiratinib DCC-2701 VEGFR , Tie-2 , FLT , Trk receptor , c-Met/HGFR
Altiratinib (DCC-2701)(DCC-2701) is a novel c-MET/TIE-2/VEGFR inhibitor; effectively reduce tumor burden in vivo and block c-MET pTyr(1349)-mediated signaling, cell growth and migration as compared with an HGF antagonist...
T1836 AZD2932 VEGFR , FLT , PDGFR , c-Kit
AZD2932 is a potent and multi-targeted kinase inhibitor VEGFR2, PDGFβ, Flt-3, and c-Kit.
T0093L Sorafenib Bay 43-9006 Apoptosis , Raf , VEGFR , FLT , Ferroptosis , PDGFR , c-Kit , Autophagy
Sorafenib (Bay 43-9006) is a multikinase inhibitor that inhibits Raf-1, B-Raf, VEGFR2, VEGFR3, VEGFR4, PDGFRβ, FLT3, c-Kit, and others (IC50=6/22/90/15/20/20/57/58 nM) with oral activity. Sorafenib has antitumor activity...
T2467 R406 free base R406 (free base) Apoptosis , FLT , Syk
R406 free base (R406 (free base)) is a potent Syk inhibitor.
T9027 CA-4948 Emavusertib IRAK , FLT
CA-4948 (Emavusertib) is a potent IRAK4/FLT3 inhibtor. CA-4948 with anti-tumor activity.
T3068 AT9283 J-504568 Apoptosis , FLT , JAK , Bcr-Abl , Aurora Kinase , Autophagy
AT9283 (J-504568) is an effective multi-targeted inhibitor of JAK2(IC50=1.2 nM) and JAK3(IC50=1.1 nM), Aurora A, Aurora B and Abl(T315I).
T41003 KG5 Raf , FLT , PDGFR , c-Kit
KG5 is a dual allosteric inhibitor of PDGFRβ and B-Raf with a Kd of 520 nM and 300 nM for PDGFRβ and PDGFRα. KG5 inhibits FLT3, KIT, and c-Raf with anticancer and antiangiogenic activities.
T2358 ENMD-2076 Apoptosis , VEGFR , FGFR , FLT , c-RET , PDGFR , Src , Aurora Kinase
ENMD-2076, a multi-targeted kinase inhibitor, has specific activity against Aurora A, Flt3, KDR/VEGFR2, Flt4/VEGFR3, FGFR1, FGFR2, Src, PDGFRα.
T2677 Crenolanib ARO 002,CP-868596 FLT , PDGFR , Autophagy
Crenolanib (ARO 002) is an orally bioavailable type III tyrosine kinases inhibitor of PDGFRα/β and FLT3 (IC50s: 11, 3.2, and 4 nM).
T8482 Ripretinib DCC-2618 Apoptosis , VEGFR , FLT , PDGFR , c-Kit
Ripretinib (DCC-2618) is an orally bioavailable inhibitor of KIT and PDGFRA.
T4209 TAK-659 hydrochloride TAK-659 VEGFR , FLT , Tyrosine Kinases , JAK , Syk
TAK-659 hydrochloride (TAK-659) is a potent and selective inhibitor of spleen tyrosine kinase (SYK) with an IC50 value of 3.2 nM. It is selective against most other kinases, but potent toward both SYK and FLT3.
T0093 Sorafenib tosylate Bay 43-9006 Apoptosis , Raf , VEGFR , FLT , Ferroptosis , PDGFR , c-Kit , Autophagy
Sorafenib tosylate (Bay 43-9006) is a potent multikinase inhibitor (IC50s: 6/20/22 nM for Raf-1/VEGFR-3/B-Raf).
T2066 Quizartinib AC220 Apoptosis , FLT , Autophagy , Ligands for Target Protein for PROTAC
Quizartinib (AC220) is an inhibitor of FLT3 (Kd: 1.6 nM) and demonstrates high selectivity for FLT3 when tested against a panel of 227 additional kinases.
T2051 SKLB4771 FLT3-​IN-​1,FLT3-IN-1 FLT
SKLB4771 (FLT3-IN-1) is a novel potent and selective Flt3 inhibitor.
T4053 AST 487 NVP-AST 487 VEGFR , FLT , c-RET , Bcr-Abl , c-Kit
AST 487 (NVP-AST 487) is a RET kinase inhibitor, inhibiting RET autophosphorylation and activation of downstream effectors. It also can inhibit Flt-3.
T2516 Amuvatinib MP470,HPK 56 Apoptosis , FLT , c-Met/HGFR , c-RET , DNA/RNA Synthesis , PDGFR , c-Kit
Amuvatinib (MP470) is an orally bioavailable synthetic carbothioamide with potential antineoplastic activity.
T6711 Tyrphostin AG1296 Tyrphostin AG 1296,AG 1296 Apoptosis , FGFR , FLT , PDGFR , c-Kit
Tyrphostin AG1296 (Tyrphostin AG 1296) is an inhibitor of PDGFR with IC50 of 0.3-0.5 μM, no activity to EGFR.
T2605 Fostamatinib Disodium Tamatinib Fosdium,R788(Disodium),R788 Disodium,R788 (Fostamatinib) Disodium FLT , Syk
Fostamatinib Disodium (R788 Disodium) is an orally available Syk kinase inhibitor with potential anti-inflammatory and immunomodulating activities.
T21503 (E/Z)-Zotiraciclib (E/Z)-TG02,(E/Z)-SB1317 FLT , JAK , CDK
(E/Z)-Zotiraciclib ((E/Z)-TG02) inhibits CDK2, JAK2, and FLT3 effectively with IC50s of 13, 73, and 56 nM, respectively.
T1667 Tandutinib MLN518,CT53518,NSC726292 Apoptosis , FLT , CSF-1R , PDGFR , Src , c-Kit
Tandutinib (CT53518) (MLN518, CT53518), an effective FLT3 antagonist (IC50: 0.22 μM), can also inhibit c-Kit and PDGFR, 15-20 fold higher potency for FLT3 versus CSF-1R and >100-fold selectivity for the same target versu...
T2586 Cabozantinib XL184,BMS-907351 Apoptosis , VEGFR , FLT , c-Met/HGFR , c-RET , TAM Receptor , c-Kit
Cabozantinib (XL184) is a multi-targeted tyrosine kinase receptor inhibitor that inhibits VEGFR2, c-Met, Kit, Axl, and Flt3 (IC50=0.035/1.3/4.6/7/11.3 nM). Cabozantinib exhibits both antitumor and antiangiogenic activity...
T4349 Sitravatinib MG516,MGCD516 Discoidin Domain Receptor (DDR) , VEGFR , FLT , Trk receptor , TAM Receptor , c-Kit , Ephrin Receptor
Sitravatinib (MGCD516) (MGCD516) is an inhibitor targeting multiple RTKs involved in driving sarcoma cell growth, including c-Met, c-Kit, PDGFRα/β, PDGFR, and Axl.
T6479 Dovitinib lactate hydrate Dovitinib (TKI258) Lactate,Dovitinib Lactate,TKI258 VEGFR , FGFR , FLT , PDGFR , c-Kit
Dovitinib lactate hydrate (TKI258) is the Lactate of Dovitinib, which is a multitargeted RTK inhibitor, mostly for class III (FLT3/c-Kit) with IC50 of 1 nM/2 nM, also potent to class IV (FGFR1/3) and class V (VEGFR1-4) R...
T2514 Linifanib ABT-869,RG3635,AL-39324 Apoptosis , c-Fms , VEGFR , FLT , CSF-1R , PDGFR , c-Kit , Autophagy
Linifanib (AL-39324) (ABT-869) is a novel, potent ATP-competitive VEGFR/PDGFR inhibitor for KDR (IC50: 4 nM), CSF-1R (IC50: 3 nM), Flt-1/3 (IC50: 3/4 nM) and PDGFRβ (IC50: 66 nM). Linifanib may exhibit potent antiprolife...

Compounds

AC1NS4RE
T2340
Synonym:
Target: Tyrosinase
FLT3-IN-2
T1938
Synonym:
Target: FLT
CCT241736
T4428
Synonym:
Target: FLT, Aurora Kinase
FLT3-IN-3
T11298
Synonym:
Target: FLT
BPR1J-097
T2272
Synonym: BPR1J097
Target: FLT
FN-1501
T15335
Synonym:
Target: FLT, CDK
AMG 925
T6756
Synonym:
Target: FLT, CDK
TCS 359
T6138
Synonym: FLT3 Inhibitor
Target: FLT
TG101209
T3065
Synonym:
Target: Apoptosis, FLT, c-RET, JAK, Autophagy
ATH686
T7673
Synonym: ATH 686
Target: Apoptosis, FLT
4SC-203
T9473
Synonym:
Target: FLT
Pacritinib
T6020
Synonym: SB1518
Target: FLT, Tyrosine Kinases, JAK
5'-Fluoroindirubinoxime
T8317
Synonym: 5'-FIO
Target: FLT
AC710
TQ0235
Synonym:
Target: FLT, PDGFR, c-Kit
Fostamatinib
T6115
Synonym: R788
Target: FLT, Syk, Monoamine Transporter, Adenosine Receptor
MRX-2843
T16144
Synonym: UNC2371
Target: Others, FLT
KW-2449
T2341
Synonym: KW2449
Target: Apoptosis, FGFR, FLT, JAK, Bcr-Abl, Src, c-Kit, Aurora Kinase
CHIR-124
T6350
Synonym: CHIR124,CHIR 124
Target: Apoptosis, GSK-3, FLT, Chk, PDGFR, Src
G-749
T2620
Synonym: G749
Target: Apoptosis, FLT, c-RET, TAM Receptor, Aurora Kinase
Merestinib
T3455
Synonym: LY2801653
Target: Discoidin Domain Receptor (DDR), FLT, c-Met/HGFR, ROS, ROS Kinase
AKN-028
T38562
Synonym:
Target: FLT
Rebastinib
T2640
Synonym: DCC2036,DCC 2036,DCC-2036
Target: Apoptosis, FLT, Bcr-Abl, Src
R406
T6174
Synonym: R-406 besylate
Target: Apoptosis, FLT, Syk
UNC2025
T7007
Synonym: mrx-6313,UNC-2025,UNC 2025
Target: FLT, TAM Receptor
Gilteritinib
T4409
Synonym: ASP2215
Target: FLT, TAM Receptor, c-Kit
Gandotinib
T2638
Synonym: LY2784544
Target: VEGFR, FGFR, FLT, JAK
Altiratinib
T2054
Synonym: DCC-2701
Target: VEGFR, Tie-2, FLT, Trk receptor, c-Met/HGFR
AZD2932
T1836
Synonym:
Target: VEGFR, FLT, PDGFR, c-Kit
Sorafenib
T0093L
Synonym: Bay 43-9006
Target: Apoptosis, Raf, VEGFR, FLT, Ferroptosis, PDGFR, c-Kit, Autophagy
R406 free base
T2467
Synonym: R406 (free base)
Target: Apoptosis, FLT, Syk
CA-4948
T9027
Synonym: Emavusertib
Target: IRAK, FLT
AT9283
T3068
Synonym: J-504568
Target: Apoptosis, FLT, JAK, Bcr-Abl, Aurora Kinase, Autophagy
KG5
T41003
Synonym:
Target: Raf, FLT, PDGFR, c-Kit
ENMD-2076
T2358
Synonym:
Target: Apoptosis, VEGFR, FGFR, FLT, c-RET, PDGFR, Src, Aurora Kinase
Crenolanib
T2677
Synonym: ARO 002,CP-868596
Target: FLT, PDGFR, Autophagy
Ripretinib
T8482
Synonym: DCC-2618
Target: Apoptosis, VEGFR, FLT, PDGFR, c-Kit
TAK-659 hydrochloride
T4209
Synonym: TAK-659
Target: VEGFR, FLT, Tyrosine Kinases, JAK, Syk
Sorafenib tosylate
T0093
Synonym: Bay 43-9006
Target: Apoptosis, Raf, VEGFR, FLT, Ferroptosis, PDGFR, c-Kit, Autophagy
Quizartinib
T2066
Synonym: AC220
Target: Apoptosis, FLT, Autophagy, Ligands for Target Protein for PROTAC
SKLB4771
T2051
Synonym: FLT3-​IN-​1,FLT3-IN-1
Target: FLT
AST 487
T4053
Synonym: NVP-AST 487
Target: VEGFR, FLT, c-RET, Bcr-Abl, c-Kit
Amuvatinib
T2516
Synonym: MP470,HPK 56
Target: Apoptosis, FLT, c-Met/HGFR, c-RET, DNA/RNA Synthesis, PDGFR, c-Kit
Tyrphostin AG1296
T6711
Synonym: Tyrphostin AG 1296,AG 1296
Target: Apoptosis, FGFR, FLT, PDGFR, c-Kit
Fostamatinib Disodium
T2605
Synonym: Tamatinib Fosdium,R788(Disodium),R788 Disodium,R788 (Fostamatinib) Disodium
Target: FLT, Syk
(E/Z)-Zotiraciclib
T21503
Synonym: (E/Z)-TG02,(E/Z)-SB1317
Target: FLT, JAK, CDK
Tandutinib
T1667
Synonym: MLN518,CT53518,NSC726292
Target: Apoptosis, FLT, CSF-1R, PDGFR, Src, c-Kit
Cabozantinib
T2586
Synonym: XL184,BMS-907351
Target: Apoptosis, VEGFR, FLT, c-Met/HGFR, c-RET, TAM Receptor, c-Kit
Sitravatinib
T4349
Synonym: MG516,MGCD516
Target: Discoidin Domain Receptor (DDR), VEGFR, FLT, Trk receptor, TAM Receptor, c-Kit, Ephrin Receptor
Dovitinib lactate hydrate
T6479
Synonym: Dovitinib (TKI258) Lactate,Dovitinib Lactate,TKI258
Target: VEGFR, FGFR, FLT, PDGFR, c-Kit
Linifanib
T2514
Synonym: ABT-869,RG3635,AL-39324
Target: Apoptosis, c-Fms, VEGFR, FLT, CSF-1R, PDGFR, c-Kit, Autophagy
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Recombinant Proteins

Cat No. Product Name Species Expression System
TMPY-01247 FLT3 Protein, Human, Recombinant (T227M, His) Human HEK293
The cluster of differentiation (CD) system is commonly used as cell markers in Immunophenotyping. Different kinds of cells in the immune system can be identified through the surface CD molecules which associating with th...
TMPK-00523 FLT3 Protein, Cynomolgus, Recombinant (hFc) Cynomolgus HEK293
The Flt-3 (fms-like tyrosine kinase) receptor, also named Flk-2 (fetal liver kinase) and Stk-1(stem cell tyrosine kinase) is a member of the class III subfamily of receptor tyrosine kinases that also includes KIT, the re...
TMPK-00416 FLT3 Protein, Human, Recombinant (His & Avi), Biotinylated Human CHO
The Flt-3 (fms-like tyrosine kinase) receptor, also named Flk-2 (fetal liver kinase) and Stk-1(stem cell tyrosine kinase) is a member of the class III subfamily of receptor tyrosine kinases that also includes KIT, the re...
TMPY-05738 FLT3 Protein, Human, Recombinant (hFc) Human HEK293
The cluster of differentiation (CD) system is commonly used as cell markers in Immunophenotyping. Different kinds of cells in the immune system can be identified through the surface CD molecules which associating with th...
TMPY-06938 FLT3 Protein, Human, Recombinant (hFc & Avi), Biotinylated Human HEK293
The cluster of differentiation (CD) system is commonly used as cell markers in Immunophenotyping. Different kinds of cells in the immune system can be identified through the surface CD molecules which associating with th...
TMPY-03704 FLT3 Protein, Mouse, Recombinant (His) Mouse HEK293
The cluster of differentiation (CD) system is commonly used as cell markers in Immunophenotyping. Different kinds of cells in the immune system can be identified through the surface CD molecules which associating with th...
TargetMol