19
1
2
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T8916 | WEE1-IN-3 | JUN76288 | Wee1 |
WEE1-IN-3 (JUN76288) is a potent Wee1 kinase inhibitor with an IC50 of <10 nM. It treatment of cancer and other proliferative diseases. | |||
T23881 | Wee1 Inhibitor II | Wee1-Inhibitor II,Wee1-Inhibitor-II,Wee1 Inhibitor-II | |
Wee1 Inhibitor II is an ATP-binding site-targeting Wee1 inhibitor. | |||
T23869 | WEE1-IN-4 | Wee1-Inhibitor-I,Wee1 Inhibitor-I,Wee1 Inhibitor I,Wee1-Inhibitor I | |
Wee1 Inhibitor I is an ATP-binding site-targeting Wee1 inhibitor. | |||
T9864 | Debio-0123 | WEE1-IN-5 | Wee1 |
Debio-0123 (WEE1-IN-5) is a potent, orally available and highly specific WEE1 inhibitor with an IC 50 in the low nanomolar range. Debio-0123 inhibits phospho-CDC2 which translated into an increase in DNA damage and prema... | |||
T6931 | PD0166285 | PD-166285 | Apoptosis , Wee1 , Chk |
PD0166285 is a potent Wee1 and Chk1 inhibitor with activity at nanomolar concentrations.PD0166285 is a novel G2 checkpoint abrogator. | |||
T2077 | Adavosertib | AZD1775,MK-1775,Adavosertib (MK-1775) | Wee1 |
Adavosertib (MK-1775) is a small molecule inhibitor of the checkpoint kinase WEE1 (IC50: 5.2 nM). It hinders the G2 DNA damage checkpoint. | |||
T9643 | ZN-c3 | Wee1 | |
ZN-c3 is a potent and selective Wee1 inhibitor with balanced potency, ADME, and pharmacokinetic properties. | |||
T41163 | ZNL 02-096 | Pomalidomide-C3-adavosertib | Apoptosis , Wee1 |
ZNL 02-096 (Pomalidomide-C3-adavosertib) is a rapid and selective degrader of Wee1 (IC50=3.58 nM).ZNL 02-096 selectively degrades Wee1 at submolar concentrations without damaging PLK1, a secondary target of AZD 1775.ZNL ... | |||
T16446 | PD 407824 | PD-407824 | Wee1 , Chk |
PD 407824 is a chemical BMP sensitiser that promotes increased cellular sensitivity to subthreshold amounts of BMP4.PD 407824 is a potent inhibitor of the checkpoint kinases Chk1 and WEE1 (IC50s: 47 and 97 nM, respective... | |||
T70126 | CJM-061 | ||
CJM-061 is a Wee1 inhibitor. | |||
T71067 | MK-1775 hemihydrate | ||
MK-1775 hemihydrate is a WEE1 inhibitor with potential antineoplastic sensitizing activity. | |||
T74371 | LEB-03-146 | ||
LEB-03-146, a WEE1 DUBTAC (deubiquitinase-targeting chimera), effectively links AZD1775 (Adavosertib) with the OTUB1 recruiter EN523 via a PEG2 linker. This compound demonstrates considerable WEE1 stabilization in HEP3B ... | |||
T74275 | LEB-03-144 | ||
LEB-03-144 is a WEE1 DUBTAC (deubiquitinase-targeting chimera) linking AZD1775 (Adavosertib) to the OTUB1 recruiter EN523 through a C3 alkyl linker. LEB-03-144 shows significant WEE1 stabilization in HEP3B hepatoma cance... | |||
T74276 | LEB-03-153 | ||
LEB-03-153 is a WEE1 DUBTAC (deubiquitinase-targeting chimera) linking AZD1775 (Adavosertib) to the OTUB1 recruiter EN523 through no linker [1] . | |||
T74274 | LEB-03-145 | ||
LEB-03-145 is a WEE1 DUBTAC (deubiquitinase-targeting chimera) linking AZD1775 (Adavosertib) to the OTUB1 recruiter EN523 through a C5 alkyl linker [1] . | |||
T71462 | GUN94110 | ||
GUN94110 is a WEE1 kinase inhibitors useful in treatment of cancer and other proliferative diseases. GUN94110 was reported in WO 2019028008. This product has no formal name at the moment. For the convenience of communica... | |||
T82385 | FMF-06-098-1 | PROTACs | |
FMF-06-098-1 is a multitargeted depressant capable of promoting the degradation of a wide array of kinases, including AAK1, ABL2, AURKA, AURKB, BUB1B, CDC7, CDK1, CDK12, CDK13, CDK2, CDK4, CDK6, CDK7, CDK9, CHEK1, CSNK1D... | |||
T74644 | DB0614 | ||
DB0614 (Example 21) is a bifunctional compound designed for the targeted degradation of kinases, effectively breaking down a wide array of kinases including AAK1, AURKA, BMP2K, CAMKK1, CDK16, CML, CDK6, EIF2AK2, FER, GAK... | |||
T6931L | PD0166285 dihydrochloride | PD-166285 | |
PD-166285 is an effective and broadly active inhibitor of protein tyrosine kinase. |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T3S0737 | Flavokawain A | Flavokavain A | Apoptosis , p38 MAPK |
NSC-37445 has anti-tumor activity, such as inhibits growth of bladder tumor cells in a nude mice model , prevents the recurrence and progression of non-muscle-invasive urothelial cell carcinoma. NSC-37445 can significant... |
Cat No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-02884 | CTDP1 Protein, Mouse, Recombinant (His & Myc) | Mouse | E. coli |
Processively dephosphorylates 'Ser-2' and 'Ser-5' of the heptad repeats YSPTSPS in the C-terminal domain of the largest RNA polymerase II subunit. This promotes the activity of RNA polymerase II. Plays a role in the exit... | |||
TMPY-04542 | CDK2 Protein, Human, Recombinant (His) | Human | Baculovirus-Insect Cells |
CDK2 is a member of the Ser/Thr protein kinase family. This protein kinase is highly similar to the gene products of S. cerevisiae cdc28, and S. pombe cdc2. It is a catalytic subunit of the cyclin-dependent protein kinas... |