141 Results for "

HT-29 cell

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

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

Cat. No.: HY-151542
CAS No.: 3031406-17-1
MLKL-IN-4 (compound 56) is a potent MLKL (Mixed lineage kinase domain-like protein) inhibitor. MLKL-IN-4 inhibits necroptosis in HT-29 cells and acts downstream of MLKL phosphorylation, with EC50 of 82 nM . MLKL-IN-4 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Cat. No.: HY-N1655
CAS No.: 873999-88-3
2,3-Dihydroamentoflavone 7,4'-dimethyl ether is a biflavonoid, which can be isolated from the aerial parts of Selaginella delicatula. 2,3-Dihydroamentoflavone 7,4'-dimethyl ether exhibits cytotoxicities against P-388 and HT-29 cell lines, with ED50 (median effective dose) values of 3.50 and 5.25 µg/mL, respectively .
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Cat. No.: HY-B1714
CAS No.: 91757-46-9
Target:  

Drug Derivative

Research Areas:  

Cancer

NSC 601980 analog is an analogue of NSC601980. In yeast screening experiments, NSC 601980 exhibited antitumor activity, effectively inhibiting cell proliferation in both COLO 205 and HT29 cell lines, with Log GI 50 values of -6.6 and -6.9, respectively.
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Cat. No.: HY-149511
CAS No.: 3125694-57-4
Target:  

c-Met/HGFR Apoptosis PDGFR

Research Areas:  

Cancer

MET/PDGFRA-IN-2 (compound 8h) is a MET and PDGFRA protein inhibitor. MET/PDGFRA-IN-2 induces cell apoptosis. MET/PDGFRA-IN-2 inhibits proliferation of MET-positive cells (IC50s: 9.7, 6.1, 12.0, 11.5, 8.6, 34.4 μM for AsPc-1, EBC-1, MKN-45, Mia-Paca-2, HT-29, K562 cells respectively) .
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Cat. No.: HY-175540
CAS No.: 3066103-58-7
Target:  

PDGFR

Research Areas:  

Cardiovascular Disease Cancer

PDGFRα kinase-IN-2 is a potent PDGFR-α inhibitor with an IC50 of 2.1 nM. PDGFRα kinase-IN-2 exhibits anticancer activity against human colon cancer HT-29 cell with an IC50 of 1.48 μM. PDGFRα kinase-IN-2 has anti-angiogenic activity in zebrafish models and low embryonic lethality. PDGFRα kinase-IN-2 can used for the studies of colon cancer and anti-angiogenesis .
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Cat. No.: HY-120528
CAS No.: 1252806-70-4
GB-110 is a potent, orally active, and nonpeptidic protease activated receptor 2 (PAR2) agonist. GB-110 selectively induces PAR2-mediated intracellular Ca 2+ release in HT29 cells with an EC50 of 0.28 μM .
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Cat. No.: HY-149510
CAS No.: 3125694-48-3
Target:  

c-Met/HGFR Apoptosis PDGFR

Research Areas:  

Cancer

MET/PDGFRA-IN-1 (compound 8c) is a MET and PDGFRA protein inhibitor (IC50: 36 μM for MET). MET/PDGFRA-IN-1 inhibits MET phosphorylation and induces cell apoptosis. MET/PDGFRA-IN-1 inhibits proliferation of MET-positive cells (IC50s: 15.3, 19.0, 22.0, 25.6, 21.0, 31.5 μM for AsPc-1, EBC-1, MKN-45, Mia-Paca-2, HT-29, K562 cells respectively) .
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Cat. No.: HY-146274
CAS No.: 2415291-03-9
Target:  

c-Met/HGFR Apoptosis

Research Areas:  

Cancer

c-Met-IN-10 (compound 26a) is a highly potent c-Met kinase inhibitor with an IC50 value of 16 nM. c-Met-IN-10 has inhibitory activity against cancer cells A549, H460 and HT-29 with IC50s of 0.56 ~ 1.59 μM. c-Met-IN-10 suppresses the colony formation on HT-29 cells, induces HT-29 and A549 cells apoptosis, and inhibits A549 cells motility. c-Met-IN-10 can be used for researching anticancer .
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Cat. No.: HY-161361
CAS No.: 3034839-17-0
Target:  

Mixed Lineage Kinase

Research Areas:  

Cancer

MLKL-IN-7 (compound 9) is a MLKL inhibitor, and shows anti-necroptosis activity in HT-29 cells with the IC50 of 148.4 nM .
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Cat. No.: HY-169735
CAS No.: 371224-09-8
Target:  

Aurora Kinase

Research Areas:  

Cancer

Aurora A inhibitor 4 (compound C9) is a potent inhibitor of Aurora A, with the GI50 of 4.26 and 7.08 μM in DU 145 cells and HT-29 cells, respectively .
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Cat. No.: HY-123707
CAS No.: 1620692-60-5
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

KPU-300 (compound 6b) is a tubulin inhibitor. KPU-300 has potent cytotoxicity with an IC50 value of 7.0 nM against HT-29 cells .
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Cat. No.: HY-W928623
CAS No.: 5351-71-3
Synonyms: ATTSC
Target:  

Bacterial

Research Areas:  

Infection Cancer

2-Acetylthiophene thiosemicarbazone is an antibacterial agent. 2-Acetylthiophene thiosemicarbazone exhibits anticancer activity, with an IC50 value of 8.6 μM against HT-29 cells .
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Cat. No.: HY-N12430
CAS No.: 858360-56-2
Marsdenoside A (compound 7) is a Marsdenoside isolated from Alocasia genus. Marsdenoside A has a weak growth inhibitory effect on two tumor cell lines, MGC-803 and HT-29, with IC50 >50 μg/mL.
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Cat. No.: HY-N3123
CAS No.: 28342-33-8
Synonyms: Dihydrooxochelerythrine
Oxychelerythrine is an alkaloid that can be isolated from Zanthoxylum integrifoliolum. Oxychelerythrine exhibits cytotoxicity against P-388 and HT-29 cell lines with ED50s of 3.25 and 5.48 μg/mL, respectively .
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Cat. No.: HY-157963
CAS No.: 3031534-16-1
Target:  

RIP kinase Necroptosis

Research Areas:  

Inflammation/Immunology Cancer

RIPK1-IN-23 (compound 19) is a RIPK1 inhibitor with potent anti-necroptotic effects in HT-29 cells (EC50 of 1.7 nM). RIPK1-IN-23 shows anti-inflammatory activities .
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Cat. No.: HY-160170
CAS No.: 2258670-86-7
Target:  

Necroptosis

Research Areas:  

Cancer

Necrosis inhibitor 3 (compound B3) is a poteng inhibitor of necrosis, with the IC50 value of 0.29 nM in HT29 cells .
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Cat. No.: HY-N12437
CAS No.: 858360-57-3
Marsdenoside B (compound 8) is a Marsdenoside isolated from Alocasia genus. Marsdenoside B inhibits the growth of tumor cell lines MGC-803 and HT-29 with IC50s of 25.6 μg/mL and 32.4 μg/mL, respectively.
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Cat. No.: HY-N14603
CAS No.: 664355-12-8
Chandrananimycin A has anti-mucor activity, as well as anti-tumor cell activity such as CCL HT29, MFXF 529L, MACL McF-7 .
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Cat. No.: HY-156775
CAS No.: 913169-79-6
Purity:  98.03%
Target:  

Drug Derivative

Research Areas:  

Cancer

Antitumor agent-119 (compound 13K) is a 2-benzoxazolyl hydrazone derivative with anticancer activities. Antitumor agent-119 inhibits the cell growth of Butkitt, CCRF-CEM, HeLa, and HT-29 with IC50 values of 30 nM, 140 nM, 100 nM, and 40 nM, respectively .
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Cat. No.: HY-161614
CAS No.: 3025180-36-0
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Tubulin inhibitor 44 (Compound 26r) is an inhibitor for tubullin. Tubulin inhibitor 44 exhibits cytotoxicity in cancer cells NCI-H460, BxPC-3 and HT-29, with IC50s of 0.96, 0.66 and 0.61 nM, respectively .
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