18 Results for "

XPO1

" in MedChemExpress (MCE) Product Catalog:
Products (18)

18 Results for "XPO1" in MCE Product Catalog:

  • Targets Recommended:
4
4 Cited Publications
Cat. No.: HY-100423
CAS No.: 1642300-52-4
Purity:  99.79%
Synonyms: KPT-8602
Target:  

CRM1

Research Areas:  

Cancer

Eltanexor (KPT-8602) is a second-generation, highly specific and orally active exportin-1 (XPO1) inhibitor with potent anti-leukemic activity. Eltanexor (KPT-8602) inhibits XPO1-dependent nuclear export (EC50=60.9 nM) by directly targeting XPO1. Eltanexor (KPT-8602) induces Caspase-dependent apoptosis in a panel of leukemic cell lines [1].
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2
2 Cited Publications
Cat. No.: HY-15970
CAS No.: 1392136-43-4
Synonyms: KPT-335
Target:  

CRM1 Apoptosis RSV

Verdinexor (KPT-335) is an orally active inhibitor for selective inhibitor of nuclear export (SINE). Verdinexor inhibits the respiratory syncytial virus A2 (RSV A2) replication with an IC50 of 0.96 µM. Verdinexor inhibits the function of nuclear export protein Exportin 1 (XPO1/CRM1), inhibiting pro-inflammatory responses. Verdinexor exhibits antitumor effciency [1] .
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Cat. No.: HY-170669
CAS No.: 3105680-00-7
Research Areas:  

Cancer

PROTAC XPO1 degrader-1 is an XPO1 degrader. PROTAC XPO1 degrader-1 exhibits anti-proliferative effects, can induce cell apoptosis, inhibit NF-κB activity, and cause cell cycle arrest in the G1 phase. PROTAC XPO1 degrader-1 can be used in research on hematological malignancies [1].
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Cat. No.: HY-144763
CAS No.: 3033267-42-1
Target:  

Apoptosis

Research Areas:  

Cancer

XPO1-IN-1 (compound D4) is an orally active and potent XPO1 inhibitor, with an IC50 of 24 nM in MM.1S cell. XPO1-IN-1 can efficiently induce cell apoptosis and cell cycle arrest. XPO1-IN-1 displays favorable metabolic stability and pharmacokinetic properties. XPO1-IN-1 can be used for multiple myeloma (MM) research [1].
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Cat. No.: HY-164710
Synonyms: b-LMB
Target:  

CRM1

Research Areas:  

Others

Biotinylated leptomycin B is a compound used to quantify nuclear export protein 1 (XPO1) occupancy and is used to study the interaction of SINE compounds with XPO1 and the response of cancer cells to related compounds.
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Cat. No.: HY-170672
CAS No.: 1076236-11-7
Research Areas:  

Cancer

XPO1-ligand-1 is a target protein ligand for XPO1 and can be used to synthesize PROTAC PROTAC XPO1 degrader-1 (HY-170669) [1].
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Cat. No.: HY-RS15889
Research Areas:  

Others

XPO1 Human Pre-designed siRNA Set A contains three designed siRNAs for XPO1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS23134
Research Areas:  

Others

Xpo1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Xpo1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-174132
Target:  

CRM1

Research Areas:  

Inflammation/Immunology

CW8001 is a covalent XPO1 (Exportin-1) inhibitor with an EC50 value of 1 nM for inhibiting T cell activation. CW8001 prevents nuclear localization of NFAT transcription factors, suppressing expression of inflammatory cytokines like IL-2. CW8001 is promising for research of T cell-driven immune diseases such as graft-versus-host disease (GVHD) [1].
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Cat. No.: HY-113902
CAS No.: 109628-38-8
Target:  

CRM1

Research Areas:  

Cancer

(2-(β-Piperidinoethyl)-9-hydroxyellipticinium chloride (compound 1AA) is a SETBP1 inhibitor that disrupts the interaction between SETBP1 and XPO1. (2-(β-Piperidinoethyl)-9-hydroxyellipticinium chloride inhibits colony formation, induces differentiation/cytotoxicity, and downregulates the transcription of Setbpl target genes. (2-(β-Piperidinoethyl)-9-hydroxyellipticinium chloride improves survival and reduces the spleen size of leukemic mice. (2-(β-Piperidinoethyl)-9-hydroxyellipticinium chloride can be used for myeloid neoplasms and solid tumors research [1].
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Cat. No.: HY-RS16700
Research Areas:  

Others

Xpo1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Xpo1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-161391
CAS No.: 1076235-18-1
Target:  

CRM1

Research Areas:  

Cancer

CW0134 (Compound 12) is a modulator for exportin1 (XPO1) ,which disrupts the chromatin binding, inhibits NFAT transcription factors and activation of T cells [1].
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Cat. No.: HY-163902
CAS No.: 154934-68-6
Target:  

CRM1

Research Areas:  

Cancer

SP100030 analogue 1 (compound 11), a SP100030 (HY-110177) analogue, is a selective inhibitor of transcriptional activation (SITA) with an EC50 of 137 nM for suppressing the XPO1-dependent upregulation of IL2 by Jurkat-based IL2-Luc reporter assay [1].
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Cat. No.: HY-161392
Target:  

CRM1

Research Areas:  

Cancer

CW2158 (Compound 13) is a modulator for exportin1 (XPO1) ,which disrupts the chromatin binding, inhibits NFAT transcription factors and activation of T cells [1].
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Cat. No.: HY-170673
CAS No.: 3105679-97-5
Research Areas:  

Cancer

E3 Ligase Ligand-linker Conjugate 156 is a CRBN E3 ligase ligand-linker conjugate. E3 Ligase Ligand-linker Conjugate 156 can be used to synthesize PROTAC XPO1 degrader-1 (HY-170669) [1].
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Cat. No.: HY-P81809
Synonyms: XPO1; CRM1; EXPOrtin-1; Exp1; Chromosome region maintenance 1 protein homolog

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, FC

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-170671
CAS No.: 1911013-66-5
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

E3 ligase Ligand 49 serves as the E3 ubiquitin ligase ligand for PROTAC XPO1 degrader-1 (HY-170669). E3 ligase Ligand 49 can be utilized for the synthesis of PROTACs [1].
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Cat. No.: HY-W010525
CAS No.: 7144-05-0
Target:  

PROTAC Linkers

Research Areas:  

Others

Piperidin-4-ylmethanamine is a PROTAC linker that can be used for the synthesis of PROTAC BRD4 Degrader-22 (HY-155393) [1].
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