24 Results for "

TACC3

" in MedChemExpress (MCE) Product Catalog:
Products (24)

24 Results for "TACC3" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-135960
CAS No.: 2408648-20-2
Pureté:  99.63%
Target:  

FGFR Apoptosis

Domaines de recherche:  

Cancer

BO-264 is a highly potent and orally active transforming acidic coiled-coil 3 (TACC3) inhibitor with an IC50 of 188 nM and a Kd of 1.5 nM. BO-264 specifically blocks the function of FGFR3-TACC3 fusion protein. BO-264 induces spindle assembly checkpoint (SAC)-dependent mitotic arrest, DNA damage and apoptosis. BO-264 has broad-spectrum antitumor activity .
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2
2 Cited Publications
Cat. No.: HY-10996A
CAS No.: 1784282-12-7
Pureté:  99.65%
KHS101 is a blood-brain barrier-penetrant anticancer agent that primarily functions by inhibiting HSPD1 (IC50 = 14.4 μM) and TACC3 across different cellular backgrounds. KHS101 promotes the aggregation of HSPD1 with client proteins, destabilizes TACC3, and reduces the levels of TACC3, Aurora A and PLK1. KHS101 induces autophagy, apoptosis, cell cycle exit and neuronal differentiation; it suppresses cancer cell growth, motility, EMT and stemness; it also impairs mitochondrial bioenergetics and glycolysis in glioblastoma cells. KHS101 can be used in research related to glioblastoma multiforme and breast cancer [3].
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1
1 Cited Publications
Cat. No.: HY-172158
CAS No.: 140481-05-6
Domaines de recherche:  

Cancer

ALKBH5-IN-5 is a highly selective ALKBH5 (IC50 = 0.62 μM, Kd = 804 nM). ALKBH5-IN-5 disrupts ALKBH5 binding to m 6A-RNA and 6mA-DNA substrates. ALKBH5-IN-5 promotes differentiation, induces apoptosis, cause G2-M phase arrest and exerts strong antiproliferative effects in cancer cells. ALKBH5-IN-5 reduces TACC3 and MYC protein levels and increases cleaved caspase-3 levels. ALKBH5-IN-5 exerts antitumor activity in tumor xenograft mice models. ALKBH5-IN-5 can be used for the research of acute myeloid leukemia .
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Cat. No.: HY-120087
CAS No.: 175205-09-1
Pureté:  99.92%
Domaines de recherche:  

Cancer

KG-548 is an ARNT/TACC3 disruptor and a HIF-1α inhibitor. KG-548 directly interferes with ARNT/TACC3 complex formation by competing with TACC3 for binding to the ARNT PAS-B domain. ARNT is the aryl hydrocarbon receptor nuclear translocator, also known as HIF-β .
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Cat. No.: HY-111876
Pureté:  99.51%
Target:  

SNIPERs

Domaines de recherche:  

Cancer

SNIPER(TACC3)-1 targets the TACC3 protein for degradation via the ubiquitin-proteasome pathway based on IAP ligand. SNIPER(TACC3)-1 induces cancer cell death .
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Cat. No.: HY-111877
Pureté:  99.81%
Target:  

SNIPERs

Domaines de recherche:  

Cancer

SNIPER(TACC3)-2 targets the TACC3 protein for degradation via the ubiquitin-proteasome pathway based on IAP ligand. SNIPER(TACC3)-2 induces cancer cell death .
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Cat. No.: HY-145895
CAS No.: 2906151-68-4
Pureté:  99.58%
Target:  

FGFR SNIPERs

Domaines de recherche:  

Cancer

SNIPER(TACC3)-11 is a potent FGFR3-TACC3 degrader. SNIPER(TACC3)-11 reduces FGFR3-TACC3 protein levels and suppressed the growth of FGFR3-TACC3 positive cancer cells .
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Cat. No.: HY-170960
CAS No.: 2642351-96-8
Domaines de recherche:  

Cancer

TACC3 inhibitor 2 is a TACC3 inhibitor with improved metabolic stability, bioavailability, and strong potency.TACC3 inhibitor 2 binds to TACC3 to modulate its function. TACC3 inhibitor 2 induces mitotic arrest, apoptosis, and DNA damage. TACC3 inhibitor 2 can be used for the research of breast cancer, colon cancer .
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Cat. No.: HY-151985
CAS No.: 3033646-06-6
Target:  

Apoptosis

Domaines de recherche:  

Cancer

TACC3 inhibitor 1 is a potent and cross the blood-brain barrier TACC3 inhibitor. TACC3 inhibitor 1 induces Apoptosis and cell cycle arrest at G2/M phase. TACC3 inhibitor 1 induces the generation of intracellular ROS. TACC3 inhibitor 1 shows antiproliferative and anti-tumor activity .
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Cat. No.: HY-RS14141
Domaines de recherche:  

Others

TACC3 Human Pre-designed siRNA Set A contains three designed siRNAs for TACC3 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS23373
Domaines de recherche:  

Others

Tacc3 Rat Pre-designed siRNA Set A contains three designed siRNAs for Tacc3 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS16930
Domaines de recherche:  

Others

Tacc3 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Tacc3 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-111877A
Target:  

SNIPERs

Domaines de recherche:  

Cancer

SNIPER(TACC3)-2 hydrochloride targets the TACC3 protein for degradation via the ubiquitin-proteasome pathway based on IAP ligand. SNIPER(TACC3)-2 hydrochloride induces cancer cell death .
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Cat. No.: HY-10996
CAS No.: 1262770-73-9
KHS101 is a blood-brain barrier-penetrant anticancer agent that primarily functions by inhibiting HSPD1 (IC50 = 14.4 μM) and TACC3 across different cellular backgrounds. KHS101 promotes the aggregation of HSPD1 with client proteins, destabilizes TACC3, and reduces the levels of TACC3, Aurora A and PLK1. KHS101 induces autophagy, apoptosis, cell cycle exit and neuronal differentiation; it suppresses cancer cell growth, motility, EMT and stemness; it also impairs mitochondrial bioenergetics and glycolysis in glioblastoma cells. KHS101 can be used in research related to glioblastoma multiforme and breast cancer [3].
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Cat. No.: HY-111886
Target:  

SNIPERs IAP

Domaines de recherche:  

Cancer

KHS108-MV1 is a conjugate of KHS108 and MV1. KHS108 is a ligand for TACC3. MV1 is an IAP antagonist that binds to cIAP1, cIAP2, and XIAP. KHS108-MV1 can be used in the research of breast cancer and fibrosarcoma .
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Cat. No.: HY-111876A
Target:  

SNIPERs

Domaines de recherche:  

Cancer

SNIPERTACC3-1 hydrochloride targets the TACC3 protein for degradation via the ubiquitin-proteasome pathway based on IAP ligand. SNIPERTACC3-1 hydrochloride induces cancer cell death .
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Cat. No.: HY-W012248
CAS No.: 349-58-6
Target:  

FGFR

Domaines de recherche:  

Cancer

KG-655 is a ligand that specifically binds to the ARNT PAS-B domain. KG-655 binds to the internal cavity of ARNT PAS-B to restrict its variable folded conformation, disrupts the interaction between ARNT PAS-B and the transcriptional coactivator TACC3, and promotes the homodimerization of ARNT PAS-B. KG-655 is widely applicable to cancer-related research .
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Cat. No.: HY-174981
Domaines de recherche:  

Cancer

LC-MF-4 is an orally active VHL-recruiting FGFR3 PROTAC degrader and hERG potassium channel inhibitor. LC-MF-4 has an IC50 of 16.6 nM against human FGFR3, exhibits inhibitory activity against hERG potassium channels, suppresses the expression of genes related to mitochondrial biogenesis and ATP synthesis, inhibits cancer cell proliferation, and shows significant antitumor activity in mice. LC-MF-4 can be used in the research of bladder cancer, urothelial carcinoma, FGFR3 Y373C mutant cancers, and FGFR3-TACC3 fusion-positive cancers .
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Cat. No.: HY-186208
CAS No.: 3115244-67-9
Target:  

Aurora Kinase

Domaines de recherche:  

Cancer

TACC3-IN-3 is a TACC3 inhibitor. TACC3 is a scaffold protein that is highly expressed in various tumors and regulates microtubule/centrosome stability via phosphorylation by Aurora A. TACC3-IN-3 inhibits the proliferation of triple-negative breast cancer cells. TACC3-IN-3 is applicable to triple-negative breast cancer research .\n
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Cat. No.: HY-186209
CAS No.: 3115244-17-9
Target:  

Aurora Kinase

Domaines de recherche:  

Cancer

TACC3-IN-4 is a TACC3 inhibitor. TACC3 is a scaffold protein that is highly expressed in various tumors and regulates microtubule/centrosome stability via phosphorylation by Aurora A. TACC3-IN-4 inhibits the proliferation of triple-negative breast cancer cells. TACC3-IN-4 can be used for triple-negative breast cancer research .
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