16 Results for "

tankyrase-1

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "tankyrase-1" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-13968
CAS No.: 664993-53-7
Purity:  99.83%
Target:  

PARP

Research Areas:  

Cancer

JW 55 is a potent and selective β-catenin signaling pathway inhibitor, which functions via inhibition of the PARP domain of tankyrase 1 and tankyrase 2 (TNKS1/2). JW 55 decreases auto-PARsylation of TNKS1/2 in vitro with IC50s of 1.9 μM and 830 nM respectively.
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3
3 Cited Publications
Cat. No.: HY-19351
CAS No.: 92831-11-3
Target:  

PARP

Research Areas:  

Cancer

MN-64 is a potent tankyrase 1 inhibitor, with IC50s of 6 nM, 72 nM, 19.1 μM, and 39.4 μM for TNKS1, TNKS2, ARTD1 and ARTD2, respectively.
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1
1 Cited Publications
Cat. No.: HY-123892
CAS No.: 2171386-10-8
Purity:  99.80%
Target:  

PARP

Research Areas:  

Cancer

RK-287107 is a potent and specific tankyrase inhibitor with IC50s of 14.3 and 10.6 nM for tankyrase-1 and tankyrase-2, respectively. RK-287107 blocks colorectal cancer cell growth [1].
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Cat. No.: HY-137849
CAS No.: 2171388-28-4
Target:  

PARP

Research Areas:  

Cancer

RK-582 is a tankyrase inhibitor, antitumor agent, and orally bioavailable growth inhibitor, with an IC50 of 36.1 nM against human tankyrase-1 and an IC50 of 39.2 nM against human tankyrase-2. In APC-mutated colorectal cancer cells, the sensitivity to RK-582 correlates with the level of active β-catenin, while drug resistance associates with PIK3CA mutation. RK-582 can be used for the research of colorectal cancer [1] .
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Cat. No.: HY-145584
CAS No.: 2055357-64-5
Purity:  99.54%
Synonyms: JPI-547/OCN-201
Target:  

PARP Wnt β-catenin

Research Areas:  

Neurological Disease Cancer

Nesuparib (JPI-547) is the orally active inhibitor for PARP 1/2 and Tankyrase 1/2 that inhibits tankyrases 1, tankyrases 2, and PARP 1 with IC50s of 5, 1 and 2 nM, respectively. Nesuparib exhibits antitumor activity and can be used in research of advanced solid tumor [1] .
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Cat. No.: HY-145267
CAS No.: 2406278-81-5
Purity:  99.59%
Target:  

PARP Wnt

Research Areas:  

Cancer

OM-153 is a potent and orally active tankyrase inhibitor with IC50s of 13 nM and 2 nM for tankyrase 1 and tankyrase 2 (TNKS1/2), respectively. OM-153 inhibits luciferase-based Wnt/β-catenin signaling reporter activity with an IC50 value of 0.63 nM. OM-153 shows inhibition of Wnt/β-catenin signaling and proliferation in COLO 320DM [1] .
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Cat. No.: HY-117705
CAS No.: 1563007-08-8
Purity:  98.88%
Target:  

Wnt PARP

Research Areas:  

Cancer

G244-LM is a potent and specific inhibitor of tankyrase 1/2 that inhibits Wnt signaling [1].
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Cat. No.: HY-152197
CAS No.: 938893-79-9
Target:  

PARP

Research Areas:  

Cancer

Tankyrase-IN-3 is a tankyrase 1 (TNKS1) inhibitor with an IC50 value of 22 nM. Tankyrase-IN-3 can be used for the research of cancer [1].
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Cat. No.: HY-145266
CAS No.: 2406276-78-4
Target:  

PARP

Research Areas:  

Cancer

OM-1700 is a potent tankyrase inhibitor with IC50s of 127 and 14 nM for tankyrase 1 and tankyrase 2, respectively. OM-1700 reduces cell growth in the colon cancer cell line COLO 320DM (GI50=650 nM) [1].
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Cat. No.: HY-108516
CAS No.: 865565-29-3
Target:  

Wnt PARP

Research Areas:  

Cancer

TC-E 5001 is an inhibitor of Wnt pathway that inhibits tankyrase 1/2 (TNKS1/2) via novel adenosine pocket binding, with Kds of 79 nM and 28 nM, respectively. TC-E 5001 also inhibits Axin2 and STF, with IC50s of 0.709 μM and 0.215 μM, respectively [1] .
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Cat. No.: HY-P701632
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: TNKS; ADP-Ribosyltransferase Diphtheria Toxin-Like 5; tankyrase; Poly [ADP-Ribose] Polymerase tankyrase-1; PARP5A; Poly [ADP-Ribose] Polymerase 5A; ARTD5; tankyrase-1; TNKS1; tankyrase I; TINF1; TNKS-1; TIN1; TANK1; PARP-5a; PARPL; PART5; TRF1-Interacting
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P701631
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: TNKS; ADP-Ribosyltransferase Diphtheria Toxin-Like 5; tankyrase; Poly [ADP-Ribose] Polymerase tankyrase-1; PARP5A; Poly [ADP-Ribose] Polymerase 5A; ARTD5; tankyrase-1; TNKS1; tankyrase I; TINF1; TNKS-1; TIN1; TANK1; PARP-5a; PARPL; PART5; TRF1-Interacting
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-152198
Target:  

PARP

Research Areas:  

Cancer

Tankyrase-IN-4 is a tankyrase 1 (TNKS1) inhibitor with an IC50 value of 0.8 nM. Tankyrase-IN-4 can be used for the research of cancer [1].
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Cat. No.: HY-P87112
Synonyms: ADP-ribosyltransferase diphtheria toxin-like 5 antibody; OTTHUMP00000115550 antibody; OTTHUMP00000224675 antibody; PARP 5a antibody; PARP5A antibody; PARPL antibody; pART5 antibody; Poly [ADP-ribose] polymerase 5A antibody; TANK 1 antibody; TANK1 antibody; ADP-ribosyltransferase diphtheria toxin-like 5 antibody; OTTHUMP00000115550 antibody; OTTHUMP00000224675 antibody; PARP 5a antibody; PARP5A antibody; PARPL antibody; pART5 antibody; Poly [ADP-ribose] polymerase 5A antibody; TANK 1 antibody; TANK1 antibody; tankyrase 1 antibody; tankyrase I antibody; tankyrase TRF1 interacting ankyrin related ADP ribose polymerase antibody; tankyrase-1 antibody; tankyrase1 antibody; tankyraseI antibody; TIN 1 antibody; TIN1 antibody; TINF 1 antibody; TINF1 antibody; TNKS 1 antibody; TNKS antibody; TNKS-1 antibody; TNKS1 antibody; TNKS1_HUMAN antibody; TRF1 interacting ankyrin related ADP ribose polymerase antibody; TRF1-interacting ankyrin-related ADP-ribose polymerase antibody;

Host:  

Rabbit

Application:  

WB

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-145584A
CAS No.: 2055357-65-6
Synonyms: JPI-547/OCN-201 hydrochloride
Target:  

PARP Wnt β-catenin

Research Areas:  

Cancer

Nesuparib (JPI-547) hydrochloride is the orally active inhibitor for PARP 1/2 and Tankyrase 1/2 that inhibits tankyrases 1, tankyrases 2, and PARP 1 with IC50s of 5, 1 and 2 nM, respectively. Nesuparib hydrochloride exhibits antitumor activity and can be used in research of advanced solid tumor [1] .
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Cat. No.: HY-183474
CAS No.: 37418-69-2
Synonyms: ZINC13406363
Target:  

Wnt β-catenin c-Myc

Research Areas:  

Cancer

LZZ-02 (ZINC13406363) is an orally active Tankyrase 1/2 inhibitor. LZZ-02 reduces c-Myc levels and inhibits the transcriptional activity of the WNT/β-catenin pathway. LZZ-02 exhibits anticancer activity against colon cancer. LZZ-02 can be used in studies related to colorectal cancer [1] .
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