S63845 MCL 1 inhibitor
Contact us: [email protected]
S63845 |
A8737-25 |
ApexBio |
25 mg |
EUR 1730.4 |
Description: S63845 is a small molecule MCL1 inhibitor with Ki < 1.2 nM [1].Myeloid cell leukemia 1 (MCL1) is a pro-survival protein and belongs to BCL-2 family proteins. |
S63845 |
A8737-5 |
ApexBio |
5 mg |
EUR 547.2 |
Description: S63845 is a small molecule MCL1 inhibitor with Ki < 1.2 nM [1].Myeloid cell leukemia 1 (MCL1) is a pro-survival protein and belongs to BCL-2 family proteins. |
Antizyme Inhibitor 1 (Antizyme inhibitor 1) Antibody |
abx230450-100ug |
Abbexa |
100 ug |
EUR 577.2 |
|
Antizyme Inhibitor 1 (Antizyme Inhibitor 1) Antibody |
20-abx111016 |
Abbexa |
|
|
|
IDO inhibitor 1 |
B8310-100 |
ApexBio |
100 mg |
EUR 1173.6 |
IDO inhibitor 1 |
B8310-25 |
ApexBio |
25 mg |
EUR 547.2 |
IDO inhibitor 1 |
B8310-5 |
ApexBio |
5 mg |
EUR 212.4 |
IDO inhibitor 1 |
A3483-10 |
ApexBio |
10 mg |
EUR 553.2 |
Description: IDO inhibitor 1 is a potent and novel indoleamine-2,3 dioxygenase (IDO) inhibitor with IC50 value <100 nM. IDO is an enzyme that catalyzes the degradation of the essential amino acid L-tryptophan to N-formylkynurenine and permits tumor cells to escape the immune system. |
IDO inhibitor 1 |
A3483-25 |
ApexBio |
25 mg |
EUR 774 |
Description: IDO inhibitor 1 is a potent and novel indoleamine-2,3 dioxygenase (IDO) inhibitor with IC50 value <100 nM. IDO is an enzyme that catalyzes the degradation of the essential amino acid L-tryptophan to N-formylkynurenine and permits tumor cells to escape the immune system. |
IDO inhibitor 1 |
A3483-5 |
ApexBio |
5 mg |
EUR 382.8 |
Description: IDO inhibitor 1 is a potent and novel indoleamine-2,3 dioxygenase (IDO) inhibitor with IC50 value <100 nM. IDO is an enzyme that catalyzes the degradation of the essential amino acid L-tryptophan to N-formylkynurenine and permits tumor cells to escape the immune system. |
IDO inhibitor 1 |
A3483-50 |
ApexBio |
50 mg |
EUR 1230 |
Description: IDO inhibitor 1 is a potent and novel indoleamine-2,3 dioxygenase (IDO) inhibitor with IC50 value <100 nM. IDO is an enzyme that catalyzes the degradation of the essential amino acid L-tryptophan to N-formylkynurenine and permits tumor cells to escape the immune system. |
IRAK inhibitor 1 |
A3500-10 |
ApexBio |
10 mg |
EUR 529.2 |
Description: IC50: 35 nM for IRAK-4The interleukin-1 receptor associated kinase (IRAK) family is comprised of four family members IRAK-1, IRAK-2, IRAK-3/M, and IRAK-4. |
IRAK inhibitor 1 |
A3500-5 |
ApexBio |
5 mg |
EUR 404.4 |
Description: IC50: 35 nM for IRAK-4The interleukin-1 receptor associated kinase (IRAK) family is comprised of four family members IRAK-1, IRAK-2, IRAK-3/M, and IRAK-4. |
IRAK inhibitor 1 |
A3500-50 |
ApexBio |
50 mg |
EUR 1280.4 |
Description: IC50: 35 nM for IRAK-4The interleukin-1 receptor associated kinase (IRAK) family is comprised of four family members IRAK-1, IRAK-2, IRAK-3/M, and IRAK-4. |
HPGDS inhibitor 1 |
B1046-1 |
ApexBio |
1 mg |
EUR 217.2 |
Description: HPGDS inhibitor 1 is an oral potent and selective inhibitor of hematopoietic prostaglandin D synthase (HPGDS) with IC50 value of 0.7nM [1].Prostaglandin D2 (PGD2) is a mediator of allergy and inflammation. |
HPGDS inhibitor 1 |
B1046-10 |
ApexBio |
10 mg |
EUR 774 |
Description: HPGDS inhibitor 1 is an oral potent and selective inhibitor of hematopoietic prostaglandin D synthase (HPGDS) with IC50 value of 0.7nM [1].Prostaglandin D2 (PGD2) is a mediator of allergy and inflammation. |
HPGDS inhibitor 1 |
B1046-5 |
ApexBio |
5 mg |
EUR 456 |
Description: HPGDS inhibitor 1 is an oral potent and selective inhibitor of hematopoietic prostaglandin D synthase (HPGDS) with IC50 value of 0.7nM [1].Prostaglandin D2 (PGD2) is a mediator of allergy and inflammation. |
DGAT-1 inhibitor |
A3363-200 |
ApexBio |
200 mg |
EUR 3208.8 |
Description: diacylglycerol acyltransferase (DGAT1) inhibitor |
DGAT-1 inhibitor |
A3363-25 |
ApexBio |
25 mg |
EUR 454.8 |
Description: diacylglycerol acyltransferase (DGAT1) inhibitor |
DGAT-1 inhibitor |
A3363-5 |
ApexBio |
5 mg |
EUR 157.2 |
Description: diacylglycerol acyltransferase (DGAT1) inhibitor |
Arginase inhibitor 1 |
B1009-10 |
ApexBio |
10 mg |
EUR 970.8 |
Description: Arginase inhibitor 1 is a novel and potent small molecule inhibitor of human arginases I and II with IC50s of 223 and 509 nM, respectively. |
Arginase inhibitor 1 |
B1009-100 |
ApexBio |
100 mg |
EUR 5706 |
Description: Arginase inhibitor 1 is a novel and potent small molecule inhibitor of human arginases I and II with IC50s of 223 and 509 nM, respectively. |
Arginase inhibitor 1 |
B1009-5 |
ApexBio |
5 mg |
EUR 582 |
Description: Arginase inhibitor 1 is a novel and potent small molecule inhibitor of human arginases I and II with IC50s of 223 and 509 nM, respectively. |
Arginase inhibitor 1 |
B1009-50 |
ApexBio |
50 mg |
EUR 3534 |
Description: Arginase inhibitor 1 is a novel and potent small molecule inhibitor of human arginases I and II with IC50s of 223 and 509 nM, respectively. |
Cathepsin Inhibitor 1 |
B2084-100 |
ApexBio |
100 mg |
EUR 1394.4 |
Description: pIC50: 7.9, 6.7, 6.0, 5.5 and 5.2 for Cathepsin (L, L2, S, K, B), respectively. |
Cathepsin Inhibitor 1 |
B2084-5 |
ApexBio |
5 mg |
EUR 224.4 |
Description: pIC50: 7.9, 6.7, 6.0, 5.5 and 5.2 for Cathepsin (L, L2, S, K, B), respectively. |
Cathepsin Inhibitor 1 |
B2084-S |
ApexBio |
Evaluation Sample |
EUR 97.2 |
Description: pIC50: 7.9, 6.7, 6.0, 5.5 and 5.2 for Cathepsin (L, L2, S, K, B), respectively. |
Ribunuclease Inhibitor / RNase Inhibitor |
105-310 |
GeneOn |
2000 u |
EUR 91.2 |
Ribunuclease Inhibitor / RNase Inhibitor |
105-350 |
GeneOn |
10000 u |
EUR 284.4 |
B-Raf inhibitor 1 |
B1172-10 |
ApexBio |
10 mg |
EUR 338.4 |
Description: B-Raf inhibitor 1 is a potent and selective B-Raf inhibitor with cell IC50s of 0.31 uM and 2 nM for A375 proliferation and A375 p-ERK respectively. |
B-Raf inhibitor 1 |
B1172-100 |
ApexBio |
100 mg |
EUR 2245.2 |
Description: B-Raf inhibitor 1 is a potent and selective B-Raf inhibitor with cell IC50s of 0.31 uM and 2 nM for A375 proliferation and A375 p-ERK respectively. |
B-Raf inhibitor 1 |
B1172-5 |
ApexBio |
5 mg |
EUR 234 |
Description: B-Raf inhibitor 1 is a potent and selective B-Raf inhibitor with cell IC50s of 0.31 uM and 2 nM for A375 proliferation and A375 p-ERK respectively. |
B-Raf inhibitor 1 |
B1172-50 |
ApexBio |
50 mg |
EUR 1274.4 |
Description: B-Raf inhibitor 1 is a potent and selective B-Raf inhibitor with cell IC50s of 0.31 uM and 2 nM for A375 proliferation and A375 p-ERK respectively. |
B-Raf Inhibitor 1 |
2599-25 |
Biovision |
each |
EUR 692.4 |
B-Raf Inhibitor 1 |
2599-5 |
Biovision |
each |
EUR 222 |
PIM-1 Inhibitor 2 |
A4519-10 |
ApexBio |
10 mg |
EUR 268.8 |
Description: Potent Pim-1 kinase inhibitor (Ki = 91 nM). |
PIM-1 Inhibitor 2 |
A4519-5 |
ApexBio |
5 mg |
EUR 205.2 |
Description: Potent Pim-1 kinase inhibitor (Ki = 91 nM). |
IRAK-1/4 Inhibitor |
9578-25 |
Biovision |
each |
EUR 705.6 |
IRAK-1/4 Inhibitor |
9578-5 |
Biovision |
each |
EUR 222 |
C-1 Inhibitor Antibody |
abx022827-10ml |
Abbexa |
10 ml |
EUR 427.2 |
|
anti-HGFA Inhibitor 1 |
YF-PA14757 |
Abfrontier |
50 ul |
EUR 435.6 |
Description: Mouse polyclonal to HGFA Inhibitor 1 |
PD-1/PD-L1 Inhibitor 1 |
B1213-25 |
Biovision |
each |
EUR 679.2 |
PD-1/PD-L1 inhibitor 1 |
B6172-25 |
ApexBio |
25 mg |
EUR 543.6 |
Description: IC50: 0.006-0.10 ?MPD-1/PD-L1 inhibitor 1 is a PD-1/PD-L1 interaction inhibitor.Plenty of studies show that blocking the PD-1/PD-Ll interactions can lead to the restorage and augment of T cell activation in many systems. |
PD-1/PD-L1 inhibitor 1 |
B6172-5 |
ApexBio |
5 mg |
EUR 201.6 |
Description: IC50: 0.006-0.10 ?MPD-1/PD-L1 inhibitor 1 is a PD-1/PD-L1 interaction inhibitor.Plenty of studies show that blocking the PD-1/PD-Ll interactions can lead to the restorage and augment of T cell activation in many systems. |
HGFA Inhibitor 1 Antibody |
DF13954 |
Affbiotech |
100ul |
EUR 420 |
HIV-1 integrase inhibitor |
A3461-10 |
ApexBio |
10 mg |
EUR 1054.8 |
Description: HIV-1 integrase inhibitor is useful for anti-HIV, with IC50 value of 0.33 µM,[1] which can target HIV-1 integrase and depress the activity in the treatment of HIV infection, AIDS, and other similar diseases characterized by integration of a retroviral genome into a host chromosome. |
HIV-1 integrase inhibitor |
A3461-100 |
ApexBio |
100 mg |
EUR 4040.4 |
Description: HIV-1 integrase inhibitor is useful for anti-HIV, with IC50 value of 0.33 µM,[1] which can target HIV-1 integrase and depress the activity in the treatment of HIV infection, AIDS, and other similar diseases characterized by integration of a retroviral genome into a host chromosome. |
HIV-1 integrase inhibitor |
A3461-5 |
ApexBio |
5 mg |
EUR 692.4 |
Description: HIV-1 integrase inhibitor is useful for anti-HIV, with IC50 value of 0.33 µM,[1] which can target HIV-1 integrase and depress the activity in the treatment of HIV infection, AIDS, and other similar diseases characterized by integration of a retroviral genome into a host chromosome. |
HIV-1 integrase inhibitor |
A3461-50 |
ApexBio |
50 mg |
EUR 2954.4 |
Description: HIV-1 integrase inhibitor is useful for anti-HIV, with IC50 value of 0.33 µM,[1] which can target HIV-1 integrase and depress the activity in the treatment of HIV infection, AIDS, and other similar diseases characterized by integration of a retroviral genome into a host chromosome. |
S63845 MCL 1 inhibitor