DYRK
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Mammalian DYRKs are a subfamily of mitogen-activated protein kinase-related protein kinases and are originally discovered on the basis of homology to the Saccharomyces cerevisiae Yak1 and Drosophila mini-brain kinases. DYRKs possess Ser/Thr phosphorylation activity as well as autophosphorylation activity on Tyr residue(s).
Two isoforms of DYRK, DYRK1A and DYRK1B, co-immunoprecipitate with HAN11 when coexpressed in COS cells indicating that the proteins interact in mammalian cells. Co-expression of DYRK1A, DYRK1B, or DYRK2 with a series of glycogen synthase mutants with Ser/Ala substitutions at the phosphorylation sites in COS cells revealed that protein kinases cause phosphorylation of site 3a in glycogen synthase. Control of glycogen synthase by DYRK represents a novel mechanism, and a potentially novel pathway, for the regulation of glycogen synthesis.
Products Related to DYRK(38)
- GC70985Dyrk1A-IN-3CAS: 2493976-27-3Purity: >99.00%
Dyrk1A-IN-3 (المركب 8b)، وهو مثبط كيناز 1A ثنائي النوعية عالي الانتقاء (DYRK1A)، يحافظ على مستويات عالية من ارتباط DYRK1A (IC50=76 نانومتر).
- GC72931HTH-01-091 TFAPurity: >98.00%
مثبط HTH-01-091 TFA هو مثبط فعال وانتقائي لسحابة الليوسين كيناز الأمومي (MELK)، مع IC50 من 10.5 نانومتر.
- GC741654-(Trifluoromethyl)aniline-d4CAS: 1219795-48-8Purity: >99.00%
4-(Trifluoromethyl)aniline-d4 هو ديوتيريوم يحمل 4-Trifluorometlaniline.
- GC74261(R)-(+)-O-DemethylbuchenavianineCAS: 1364123-68-1Purity: >98.00%
(R)-(+)-O-Demethylbuchenavianine هو مثبط للكيناز المعتمد على السايكلين CDK.
- GC81300PROTAC DYRK2 degrader-2CAS: 3061366-74-0Purity: >98.00%
PROTAC DYRK2 degrader-2 is a PROTAC DYRK2 degrader based on curcumin analog A3.
- GC81307DYRK2-IN-2CAS: 2416195-65-6Purity: >98%
DYRK2-IN-2 (Compound C17) is a selective inhibitor of DYRK2, with its IC 50 value being 40.3 nM.
- GC81308DYRK2-IN-2 hydrochloridePurity: >98.00%
DYRK2-IN-2 hydrochloride is a selective DYRK2 inhibitor with an IC 50 of 40.3 nM.
- GC81309AO-365/43472821CAS: 1081122-55-5Purity: >99.50%
AO-365/43472821 is a selective, brain-penetrant Dual-specificity tyrosine phosphorylation-regulated kinase 1A ( DYRK1A ) inhibitor ( IC 50 = 0.29 μM) and shows a significant inhibitory effect on ( CDC-like kinase 1) CLK1 ( IC 50 = 0.08 μM).
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC70625 | AnnH31 | 241809-12-1 | >99.00% | |
AnnH31 هو مثبط Dyrk1A (IC50: 81 نانومتر). | ||||
| GC70985 | Dyrk1A-IN-3 | 2493976-27-3 | >99.00% | |
Dyrk1A-IN-3 (المركب 8b)، وهو مثبط كيناز 1A ثنائي النوعية عالي الانتقاء (DYRK1A)، يحافظ على مستويات عالية من ارتباط DYRK1A (IC50=76 نانومتر). | ||||
| GC71197 | FINDY | 1507367-37-4 | - | |
FINDY هو مثبط انتقائي متوسط قابل للطي لـ DYRK1A. | ||||
| GC72931 | HTH-01-091 TFA | - | >98.00% | |
مثبط HTH-01-091 TFA هو مثبط فعال وانتقائي لسحابة الليوسين كيناز الأمومي (MELK)، مع IC50 من 10.5 نانومتر. | ||||
| GC72982 | BT173 | 2232180-74-2 | >98.00% | |
يعتبر BT173 مثبط فعال لتفاعل المجال homeodomain للبروتين كيناز 2 (HIPK2). | ||||
| GC73224 | CLK1-IN-3 | 2922550-28-3 | >98.00% | |
CLK1-IN-3 (المركب 10ad) هو مثبط قوي وانتقائي Clk1، مع IC50 من 5 نانومتر وأكثر من 300 مرة انتقائية ل Dyrk1A. | ||||
| GC73707 | ON 108600 | 1585246-23-6 | >99.00% | |
يعتبر ON 108600 مثبط لـ CK2 (Casein Kinase2)/TNIK/DYRK1، مع IC50 لـ DYRK1A/DYRKB و DYRK2 و CK2α1/CK2α2 و TNIK من 0.016 ميكرومتر/0.007 ميكرومتر و 0.028 ميكرومتر و 0.05 ميكرومتر/0.005 ميكرومتر و 0.005 ميكرومتر على التوالي. | ||||
| GC74165 | 4-(Trifluoromethyl)aniline-d4 | 1219795-48-8 | >99.00% | |
4-(Trifluoromethyl)aniline-d4 هو ديوتيريوم يحمل 4-Trifluorometlaniline. | ||||
| GC74261 | (R)-(+)-O-Demethylbuchenavianine | 1364123-68-1 | >98.00% | |
(R)-(+)-O-Demethylbuchenavianine هو مثبط للكيناز المعتمد على السايكلين CDK. | ||||
| GC80874 | ARN25699 | - | >98% | |
ARN25699 is a kinase inhibitor with an IC 50 of 5.5 nM against GSK-3β, 2.2 nM against FYN-α, and 242.3 nM against DYRK1A, and it exhibits oral bioavailability. | ||||
| GC81300 | PROTAC DYRK2 degrader-2 | 3061366-74-0 | >98.00% | |
PROTAC DYRK2 degrader-2 is a PROTAC DYRK2 degrader based on curcumin analog A3. | ||||
| GC81307 | DYRK2-IN-2 | 2416195-65-6 | >98% | |
DYRK2-IN-2 (Compound C17) is a selective inhibitor of DYRK2, with its IC 50 value being 40.3 nM. | ||||
| GC81308 | DYRK2-IN-2 hydrochloride | - | >98.00% | |
DYRK2-IN-2 hydrochloride is a selective DYRK2 inhibitor with an IC 50 of 40.3 nM. | ||||
| GC81309 | AO-365/43472821 | 1081122-55-5 | >99.50% | |
AO-365/43472821 is a selective, brain-penetrant Dual-specificity tyrosine phosphorylation-regulated kinase 1A ( DYRK1A ) inhibitor ( IC 50 = 0.29 μM) and shows a significant inhibitory effect on ( CDC-like kinase 1) CLK1 ( IC 50 = 0.08 μM). | ||||
