141 Results for "

HT-29 cell

" in MedChemExpress (MCE) Product Catalog:
Products (141)

141 Results for "HT-29 cell" in MCE Product Catalog:

14
14 Publications Verification
Cat. No.: HY-13734
CAS No.: 141400-58-0
Purity:  99.87%
Synonyms: IV-2
Target:  

Apoptosis

Research Areas:  

Cancer

PX-12(IV-2) is an irreversible inhibitor of Thioredoxin-1 (Trx-1); inhibits the growth of MCF-7 and HT-29 cells with IC50 values of 1.9 and 2.9 μM, respectively.
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11
11 Cited Publications
Cat. No.: HY-100753
CAS No.: 2059952-75-7
Purity:  96.28%
Target:  

STAT Apoptosis

Research Areas:  

Cancer

STAT3-IN-1 (compound 7d) is an excellent, selective and orally active STAT3 inhibitor, with IC50 values of 1.82 μM and 2.14 μM in HT29 and MDA-MB 231 cells, respectively. STAT3-IN-1 (compound 7d) induces tumor cells apoptosis .
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4
4 Cited Publications
Cat. No.: HY-139206
CAS No.: 2452464-73-0
Purity:  99.65%
Synonyms: IL-17A inhibitor 1
Target:  

Interleukin Related

Research Areas:  

Inflammation/Immunology

LY3509754 (IL-17A inhibitor 1) is a IL-17A inhibitor, with IC50 values of <9.45 nM and 9.3 nM in alphalisa assay and HT-29 cells .
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4
4 Cited Publications
Cat. No.: HY-12855A
CAS No.: 1391426-24-6
Purity:  99.89%
Synonyms: Lys01 trihydrochloride
Target:  

Autophagy

Research Areas:  

Cancer

Lys05 (Lys01 trihydrochloride) is a novel lysosomal autophagy inhibitor with IC50 values of 3.6, 3.8, 6 and 7.9 μM for 1205Lu, c8161, LN229 and HT-29 cell line in the MTT assay.
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4
4 Cited Publications
Cat. No.: HY-101524
CAS No.: 2093393-05-4
Purity:  99.04%
Target:  

Mixed Lineage Kinase

Research Areas:  

Cancer

TC13172 is a mixed lineage kinase domain-like protein (MLKL) inhibitor with an EC50 value of 2 nM for HT-29 cells .
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4
4 Cited Publications
Cat. No.: HY-14444
CAS No.: 714272-27-2
Purity:  ≥98.0%
Synonyms: NPI-2358
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Plinabulin (NPI-2358) is a vascular disrupting agen (VDA) against tubulin-depolymerizing with an IC50 of 9.8 nM against HT-29 cells . Plinabulin binds the colchicine binding site of β-tubulin preventing polymerization and has potent inhibitory to tumor cells .
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1
1 Cited Publications
Cat. No.: HY-107664
CAS No.: 184162-64-9
Purity:  99.16%
Research Areas:  

Neurological Disease

SR 142948 is an orally active and selective non-peptide neurotensin receptor (NT) antagonist with IC50s of 1.19 nM, 0.32 nM, 3.96 nM in h-NTR1-CHO cells, HT-29 cells, and adult rat brain, respectively. SR 142948 antagonizes NT-induced inositol monophosphate formation in HT-29 cells with an IC50 of 3.9 nM. SR 142948 blocks hypothermia, analgesia and steering behavior induced by NT in vivo. SR 142948 shows blood-brain permeability and can be used in study of psychiatric disorders .
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1
1 Cited Publications
Cat. No.: HY-N6002
CAS No.: 475231-21-1
Category:  

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