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FLT

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225

Inhibitors & Agonists

1

Screening Libraries

1

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1

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3

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2

Inhibitory Antibodies

3

Natural
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54

Recombinant Proteins

9

Isotope-Labeled Compounds

1

Antibodies

Targets Recommended:
Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-B1516

    3'-Fluoro-3'-deoxythymidine; 3′-Deoxy-3′-fluorothymidine; FLT

    Alovudine (3'-Fluoro-3'-deoxythymidine) is a marker of DNA synthesis that is less susceptible to inflammatory changes than 18F-Fluorodeoxyglucose (FDG) and thus is a better biomarker in pancreatic cancer. Alovudine shows anti-orthopoxvirus activity .
    Alovudine
  • HY-162032

    FLT3 Cancer
    FLT3-IN-25 (compound 17) is a potent inhibitor of FLT3, with IC50s of 1.2 nM, 1.4 nM and 1.1 nM for FLT3-WT, FLT3-D835Y and FLT3-ITD, respectively. FLT3-IN-25 plays an important role in acute myeloid leukemia (AML) .
    <em>FLT</em>3-IN-25
  • HY-144777

    FLT3 Apoptosis Cancer
    FLT3-IN-14 is a potent FLT3 inhibitor with IC50s of 5.6 nM and 1.4 nM for FLT3-WT and FLT3-ITD. FLT3-IN-14 reduces the phosphorylation of FLT3 (Y591), induces cell cycle arrest at G1 phase and apoptosis. FLT3-IN-14 significantly reduces the tumor growth in an MV4-11 xenograft mouse model .
    <em>FLT</em>3-IN-14
  • HY-156410

    FLT3 Cancer
    FLT3-IN-23 (compound 15) is an inhibitor of JFMS-like tyrosine kinase 3 (FLT3) with an IC50 of 7.42 nM. FLT3-IN-23 has antiproliferative activities against BaF3 cells carrying various FLT3-TKD and FLT3-ITD-TKD mutations .
    <em>FLT</em>3-IN-23
  • HY-155770

    FLT3 Cancer
    FLT3-IN-20 (compound 34f) is a potent FLT3 inhibitor with IC50 values of 1 and 4 nM for FLT3-D835Y and FLT3-ITD, respectively. FLT3-IN-20 has anti-proliferation efficacy in FLT3-ITD-positive AML cell lines MV4-11 and MOLM-13 (7 and 9 nM, respectively) and the MOLM-13 variant (4 nM) with the FLT3-ITD-D835Y mutation. FLT3-IN-20 can be used in research of cancer .
    <em>FLT</em>3-IN-20
  • HY-148522

    FLT3 Cancer
    FLT3-IN-18 is a potent and selective FLT3 inhibitor with an IC50 value of 0.003 μM. FLT3-IN-18 induces apoptosis and cell cycle arrest at G1 phase. FLT3-IN-18 inhibits FLT3 and STAT5 phosphorylation. FLT3-IN-18 has the potential for the research of acute myeloid leukemia (AML) .
    <em>FLT</em>3-IN-18
  • HY-112475

    Tie FLT3 Cancer
    Flt-3 Inhibitor III is a potent and selective FLT3 kinase inhibitor with an 50 of 50 nM. Flt-3 Inhibitor III shows less active against other kinases. Flt-3 Inhibitor III has anticancer effects .
    <em>Flt</em>-3 Inhibitor III
  • HY-128572

    FLT3 Cancer
    FLT3-IN-6 is a potent and selective inhibitor of FLT3-ITD (FLT3 mutation) with an IC50 of 1.336 nM .
    <em>FLT</em>3-IN-6
  • HY-134481

    FLT3 Cancer
    FLT3-IN-10 (compound 7c) is a potent inhibitor of FMS-like tyrosine kinase 3 (FLT3). FLT3-IN-10 has the potential for the research of FLT3-mutated acute myeloid leukemia (AML) .
    <em>FLT</em>3-IN-10
  • HY-146886

    FLT3 Cancer
    FLT3-IN-15 is a highly potent and orally active FLT3 inhibitor with IC50s of 0.87 nM and 0.32 nM for FLT3 and FLT3/D835Y, respectively. FLT3-IN-15 can be used for researching acute myeloid leukemia .
    <em>FLT</em>3-IN-15
  • HY-155302

    FLT3 Cancer
    FLT3-IN-22 (compound 22f) is a potent FLT3 inhibitor with IC50 values of 0.941 nM and 0.199 nM for FLT3 and FLT3/D835Y, respectively. FLT3-IN-22 exhibits strong antiproliferative activity against MV4-11 cells and the mutant FLT kinase expressed Ba/F3 cell lines, including FLT-D835Y and FLT3-F691L .
    <em>FLT</em>3-IN-22
  • HY-112145

    FLT3 Cancer
    FLT3-IN-3 is a potent FLT3 inhibitor with IC50s of 13 and 8 nM for FLT3 WT and FLT3 D835Y, respectively.
    <em>FLT</em>3-IN-3
  • HY-143895

    FLT3 Cancer
    FLT3-IN-12 is a potent, selective and orally active FLT3 kinase inhibitor with IC50s of 1.48 nM and 2.87 nM for FLT3-WT and FLT3-D835Y, respectively. FLT3-IN-12 possesses high selectivity over c-KIT (>1000-fold). FLT3-IN-12 has an excellent anti-AML (acute myeloid leukemia) activity (MV4-11, IC50 of 0.75 nM) .
    <em>FLT</em>3-IN-12
  • HY-148036

    FLT3 Cancer
    FLT3-IN-16 is a potent FLT3 inhibitor with an IC50 of 1.1 μM. FLT3-IN-16 can be used for researching acute myeloid leukemia .
    <em>FLT</em>3-IN-16
  • HY-143894

    FLT3 Cancer
    FLT3-IN-11 (compound 30) is a potent, selective and orally active FLT3 kinase inhibitor with IC50s of 7.22 nM and 4.95 nM for wild-type FLT3 and FLT3-D835Y, respectively. FLT3-IN-11 high selectivity for FLT3 over c-KIT (>1000-fold). FLT3-IN-11has excellent anti-acute myeloid leukemia (AML) activity (MV4-11 cells, IC50 of 3.2 nM) .
    <em>FLT</em>3-IN-11
  • HY-153473

    FLT3 Cancer
    FLT3-IN-19 (Comp 50) is a potent and selective FLT3 inhibitor with IC50 of 0.213 nM. FLT3-IN-19 can be used in AML disease research .
    <em>FLT</em>3-IN-19
  • HY-163068

    FLT3 Cancer
    FLT3-IN-24 (compound 24) is a potent and selective inhibitor of FLT3 kinase with an IC50 of 7.94 nM. FLT3-IN-24 has cell antiproliferative effects .
    <em>FLT</em>3-IN-24
  • HY-144710

    FLT3 Cancer
    FLT3/ITD-IN-2 (Compound 17) is a potent FLT3 internal tandem duplications (FLT3-ITD) inhibitor with IC50 values of 0.3, 0.4 and 1.0 nM against FLT3 D835Y, FLT3 and FLT3-ITD, respectively. FLT3/ITD-IN-2 potently inhibits the phosphorylation of FLT3 and displays excellent antiproliferative activities against acute myeloid leukemia cell lines .
    <em>FLT</em>3/ITD-IN-2
  • HY-144711

    FLT3 Cancer
    FLT3/ITD-IN-3 (Compound 19) is a potent FLT3 internal tandem duplications (FLT3-ITD) inhibitor with IC50 values of 0.3, 0.4 and 0.9 nM against FLT3 D835Y, FLT3 and FLT3-ITD, respectively. FLT3/ITD-IN-3 potently inhibits the phosphorylation of FLT3 and displays excellent antiproliferative activities against acute myeloid leukemia cell lines .
    <em>FLT</em>3/ITD-IN-3
  • HY-144709

    FLT3 Cancer
    FLT3/ITD-IN-1 (Compound 1) is a potent FLT3 internal tandem duplications (FLT3-ITD) inhibitor with IC50 values of 38.2 nM and 144.1 nM against FLT3 and FLT3-ITD, respectively. FLT3/ITD-IN-1 displays excellent antiproliferative activities against acute myeloid leukemia cell lines .
    <em>FLT</em>3/ITD-IN-1
  • HY-148070

    FLT3 FAK Cytochrome P450 Cancer
    FLT3-IN-17 inhibits CYPs and FLT3 mutants activity (IC50s: <0.5 nM for D835Y). FLT3-IN-17 is also a FAK inhibitor, with an IC50 value of 12 nM. FLT3 ligand-2 can be used in the research of cancers .
    <em>FLT</em>3-IN-17
  • HY-155226

    FLT3 Apoptosis Cancer
    FLT3-IN-21 (compound LC-3) is a potent FLT3 inhibitor (IC50: 8.4 nM) and induces apoptosis. FLT3-IN-21 can arrest the cell cycle in the G1 phase and inhibit the proliferation of FLT3-ITD-positive AML cells MV-4-11 (IC50: 5.3 nM). In mice, FLT3-IN-21 (10 mg/kg/d) inhibited tumor growth in the MV-4-11 xenograft model (TGI=92.16%) .
    <em>FLT</em>3-IN-21
  • HY-146749

    FLT3 Trk Receptor Apoptosis Cancer
    FLT3/TrKA-IN-1 is a potent FLT3/TrKA dual kinase inhibitor with the IC50s of 43.8 nM, 97.2 nM, 92.5 nM and 23.6 nM for FLT3, FLT3-ITD, FLT3-TKD and TrKA, respectively. FLT3/TrKA-IN-1 induces cell cycle arrest at the G0/G1 phase as well as apoptosis and shows antiproliferative activity in vitro. FLT3/TrKA-IN-1 has the potential for the research of Acute myeloid leukemia (AML) .
    <em>FLT</em>3/TrKA-IN-1
  • HY-143278

    Topoisomerase FLT3 Apoptosis Cancer
    FLT3-IN-13 (compound 20) is a potent and effective antileukemic topoisomerase II and FLT3 dual inhibitor with IC50 values of 2.26 μM and 2.26 μM, respectively. FLT3-IN-13 arrests cell cycle at G2/M phase and induce apoptosis. FLT3-IN-13 has anticytotoxic activity, particularly against leukemia .
    <em>FLT</em>3-IN-13
  • HY-146680

    FLT3 RET CDK MAP4K Cancer
    FLT3/ITD-IN-4 (Compound 16) is a selective FMS-like tyrosine kinase 3 internal tandem duplications (FLT3-ITD) inhibitor with an IC50 of 2.3 nM. FLT3/ITD-IN-4 can be used for acute myeloid leukemia research .
    <em>FLT</em>3/ITD-IN-4
  • HY-18744

    FLT3 Cancer
    FLT3-IN-2 is a FLT3 inhibitor with IC50 of < 1 μM, detailed information refer to WO 2012158957 A2 and WO 2007013896.
    <em>FLT</em>3-IN-2
  • HY-162367

    FLT3 Checkpoint Kinase (Chk) Cancer
    FLT3/CHK1-IN-2 (Compound 30) is a dual inhibitor of FLT3 and CHK1, with IC50s of 25.63, 16.39, 22.80 nM for CHK1, FLT3-WT, and FLT-D835Y respectively. FLT3/CHK1-IN-2 has favorable oral PK properties and kinase selectivity. FLT3/CHK1-IN-2 can be used for research of acute myeloid leukemia (AML) .
    <em>FLT</em>3/CHK1-IN-2
  • HY-115904

    CDK FLT3 Cancer
    FLT3/CDK4-IN-1 is a potent, high selective and orally active FLT3/CDK4 dual inhibitor (IC50=11 and 7 nM for FLT3 and CDK4, respectively). FLT3/CDK4-IN-1 has antiproliferative activities against certain cancer cells. FLT3/CDK4-IN-1 has good antitumor effect in vivo .
    <em>FLT</em>3/CDK4-IN-1
  • HY-128571

    FLT3 Cancer
    FLT3-IN-4 is a potent and orally effective Fms-like tyrosine receptor kinase 3 (FLT3; IC50=7 nM) inhibitor for treating acute myelogenous leukemia .
    <em>FLT</em>3-IN-4
  • HY-155195

    Others Cancer
    FLT3/CHK-IN-1 (Compound 18) is a dual inhibitor of FLT3/CHK1. FLT3/CHK-IN-1 is more than 1700 times more selective to c-KI T and greatly reduces hERG affinity with an IC50 value of 58.4 μM. FLT3/CHK-IN-1 inhibits tumor growth in mouse xenotransplantation models inoculated with MV-4-11 cells .
    <em>FLT</em>3/CHK1-IN-1
  • HY-161323

    FLT3 Bcr-Abl Apoptosis Cancer
    FLT3-ITD/D835Y-IN-1 (Compound 1) is a FLT3-ITD and BCR-ABL inhibitor. FLT3-ITD/D835Y-IN-1 mediates proapoptosis by inhibiting the FLT3 and BCR-ABL pathways, as well as other possible targets. FLT3-ITD/D835Y-IN-1 can be used in the study of acute myeloid leukemia (AML) .
    <em>FLT</em>3-ITD/D835Y-IN-1
  • HY-143434

    FLT3 Cancer
    FLT3/D835Y-IN-1 (compound 13a) is a orally active, potent and selective FLT3 and FLT3/D835Y inhibitor, with IC50 values of 0.26 nM and 0.18 nM, respectively. FLT3/D835Y-IN-1 also blocks tumor growth, has anticancer efficacy, and can be used to research for AML (acute myeloid leukemia) .
    <em>FLT</em>3/D835Y-IN-1
  • HY-12960

    FLT3-​IN-​1

    FLT3 c-Kit Apoptosis Cancer
    SKLB4771 is a potent and selective Flt3 inhibitor with an IC50 value of 10 nM. SKLB4771 downregulates the phosphorylation of FLT3/STAT5/ERK, blocks cell proliferation, and induces apoptosis in tumor tissue .
    SKLB4771
  • HY-RS04987

    Small Interfering RNA (siRNA) Others

    FLT1 Human Pre-designed siRNA Set A contains three designed siRNAs for FLT1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    FLT1 Human Pre-designed siRNA Set A
    FLT1 Human Pre-designed siRNA Set A
  • HY-RS04988

    Small Interfering RNA (siRNA) Others

    Flt1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Flt1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Flt1 Mouse Pre-designed siRNA Set A
    Flt1 Mouse Pre-designed siRNA Set A
  • HY-RS04989

    Small Interfering RNA (siRNA) Others

    Flt1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Flt1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Flt1 Rat Pre-designed siRNA Set A
    Flt1 Rat Pre-designed siRNA Set A
  • HY-RS04990

    Small Interfering RNA (siRNA) Others

    FLT3 Human Pre-designed siRNA Set A contains three designed siRNAs for FLT3 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    FLT3 Human Pre-designed siRNA Set A
    FLT3 Human Pre-designed siRNA Set A
  • HY-RS04991

    Small Interfering RNA (siRNA) Others

    Flt3 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Flt3 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Flt3 Mouse Pre-designed siRNA Set A
    Flt3 Mouse Pre-designed siRNA Set A
  • HY-RS04992

    Small Interfering RNA (siRNA) Others

    Flt3 Rat Pre-designed siRNA Set A contains three designed siRNAs for Flt3 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Flt3 Rat Pre-designed siRNA Set A
    Flt3 Rat Pre-designed siRNA Set A
  • HY-RS04994

    Small Interfering RNA (siRNA) Others

    FLT4 Human Pre-designed siRNA Set A contains three designed siRNAs for FLT4 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    FLT4 Human Pre-designed siRNA Set A
    FLT4 Human Pre-designed siRNA Set A
  • HY-RS04995

    Small Interfering RNA (siRNA) Others

    Flt4 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Flt4 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Flt4 Mouse Pre-designed siRNA Set A
    Flt4 Mouse Pre-designed siRNA Set A
  • HY-RS04996

    Small Interfering RNA (siRNA) Others

    Flt4 Rat Pre-designed siRNA Set A contains three designed siRNAs for Flt4 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Flt4 Rat Pre-designed siRNA Set A
    Flt4 Rat Pre-designed siRNA Set A
  • HY-RS04993

    Small Interfering RNA (siRNA) Others

    FLT3LG Human Pre-designed siRNA Set A contains three designed siRNAs for FLT3LG gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    FLT3LG Human Pre-designed siRNA Set A
    FLT3LG Human Pre-designed siRNA Set A
  • HY-148521

    CDK FLT3 PROTACs Apoptosis Cancer
    PROTAC FLT3/CDK9 degrader-1 is a potent FLT3 and CDK9 dual PROTAC degrader. PROTAC FLT3/CDK9 degrader-1 induces apoptosis and effective degradation of target proteins FLT3 and CDK9. PROTAC FLT3/CDK9 degrader-1 has the potential for the research of FLT3-ITD mutated AML .
    PROTAC <em>FLT</em>3/CDK9 degrader-1
  • HY-130247
    JAK2/FLT3-IN-1
    1 Publications Verification

    JAK FLT3 Apoptosis Cancer
    JAK2/FLT3-IN-1 is a potent and orally active dual JAK2/FLT3 inhibitor with IC50 values of 0.7 nM, 4 nM, 26 nM and 39 nM for JAK2, FLT3, JAK1 and JAK3, respectively. JAK2/FLT3-IN-1 has anti-cancer activity .
    JAK2/<em>FLT</em>3-IN-1
  • HY-161280

    PROTACs FLT3 Cancer
    PROTAC FLT-3 degrader 3 (compound 35) is a PROTACs degrader of FLT. PROTAC FLT-3 degrader 3 has antiproliferative activity, with IC50 of 7.55 nM in MV4-11 cells .
    PROTAC <em>FLT</em>-3 degrader 3
  • HY-130247A
    JAK2/FLT3-IN-1 TFA
    1 Publications Verification

    JAK FLT3 Apoptosis Cancer
    JAK2/FLT3-IN-1 (TFA) is a potent and orally active dual JAK2/FLT3 inhibitor with IC50 values of 0.7 nM, 4 nM, 26 nM and 39 nM for JAK2, FLT3, JAK1 and JAK3, respectively. JAK2/FLT3-IN-1 (TFA) has anti-cancer activity .
    JAK2/<em>FLT</em>3-IN-1 TFA
  • HY-114323

    PROTACs FLT3 Apoptosis Cancer
    PROTAC FLT-3 degrader 1 is a von Hippel-Lindau-based PROTAC FLT-3 internal tandem duplication (ITD) degrader with an IC50 0.6 nM. Anti-proliferative activity; apoptosis induction .
    PROTAC <em>FLT</em>-3 degrader 1
  • HY-145903

    PDGFR FLT3 Cancer
    PDGFRα/FLT3-ITD-IN-2 (Compound 13d) is a potent inhibitor of PDGFRα/FLT3 with IC50s of more than 20 and 1.654 μM, respectively. PDGFRα/FLT3-ITD-IN-2 has the potential for the research of acute myeloid leukemia or chronic eosinophilic leukemia .
    PDGFRα/<em>FLT</em>3-ITD-IN-2
  • HY-145904

    PDGFR FLT3 Cancer
    PDGFRα/FLT3-ITD-IN-3 (Compound 18d) is a potent inhibitor of PDGFRα/FLT3 with IC50s of 0.153 and 0.004 μM, respectively. PDGFRα/FLT3-ITD-IN-3 has the potential for the research of acute myeloid leukemia or chronic eosinophilic leukemia .
    PDGFRα/<em>FLT</em>3-ITD-IN-3

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