S63845 MCL 1 inhibitor

S63845 MCL 1 inhibitor

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S63845

A8737-25 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 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.

S63845

HY-100741 100mg
EUR 2043.6

Antizyme Inhibitor 1 (Antizyme inhibitor 1) Antibody

abx230450-100ug 100 ug
EUR 577.2

Antizyme Inhibitor 1 (Antizyme Inhibitor 1) Antibody

20-abx111016
  • EUR 878.40
  • EUR 477.60
  • 150 ul
  • 50 ul

EMT inhibitor-1

HY-101275 5mg
EUR 680.4

EED inhibitor-1

HY-103663 10mM/1mL
EUR 207.6

Cot inhibitor-1

HY-32015 10mg
EUR 670.8

DAAO inhibitor-1

HY-111412 10mM/1mL
EUR 392.4

CNT2 inhibitor-1

HY-112843 25mg
EUR 2469.6

mTOR inhibitor-1

HY-112914 10mg
EUR 680.4

Grp94 Inhibitor-1

HY-112910 50mg
EUR 391.2

Kinase inhibitor-1

HY-43533 5mg
EUR 680.4

IDO inhibitor 1

B8310-100 100 mg
EUR 1173.6

IDO inhibitor 1

B8310-25 25 mg
EUR 547.2

IDO inhibitor 1

B8310-5 5 mg
EUR 212.4

IDO inhibitor 1

A3483-10 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 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 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 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.

Src Inhibitor 1

HY-101053 50mg
EUR 712.8

ALK inhibitor 1

HY-15357 50mg
EUR 1712.4

Btk inhibitor 1

HY-13036 50mg
EUR 2539.2

IRAK inhibitor 1

A3500-10 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 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 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.

FAAH inhibitor 1

HY-10862 5mg
EUR 392.4

CCR6 inhibitor 1

HY-112701 10mg
EUR 1093.2

p38α inhibitor 1

HY-114423 5mg
EUR 267.6

IRAK inhibitor 1

HY-13275 10mM/1mL
EUR 500.4

HPGDS inhibitor 1

B1046-1 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 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 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

A3363-200 200 mg
EUR 3208.8
Description: diacylglycerol acyltransferase (DGAT1) inhibitor

DGAT-1 inhibitor

A3363-25 25 mg
EUR 454.8
Description: diacylglycerol acyltransferase (DGAT1) inhibitor

DGAT-1 inhibitor

A3363-5 5 mg
EUR 157.2
Description: diacylglycerol acyltransferase (DGAT1) inhibitor

HPGDS inhibitor 1

HY-10439 5mg
EUR 391.2

PI3Kγ inhibitor 1

HY-10549 50mg
EUR 2539.2

LRRK2 inhibitor 1

HY-111493 50mg
EUR 3159.6

MAT2A inhibitor 1

HY-112131 10mg
EUR 1093.2

SIRT5 inhibitor 1

HY-112634 10mM/1mL
EUR 1184.4

PI3kδ inhibitor 1

HY-15288 5mg
EUR 652.8

Tubulin inhibitor 1

HY-112607 50mg
EUR 2332.8

YAP/TAZ inhibitor-1

HY-111429 10mg
EUR 817.2

Arginase inhibitor 1

B1009-10 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

B1009-100 100 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 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 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.

Thrombin inhibitor 1

HY-U00370 1mg
EUR 2804.4

Arginase inhibitor 1

HY-15775 50mg
EUR 2704.8

Cathepsin Inhibitor 1

B2084-100 100 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 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 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 2000 u
EUR 91.2

Ribunuclease Inhibitor / RNase Inhibitor

105-350 10000 u
EUR 284.4

B-Raf inhibitor 1

B1172-10 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

B1172-100 100 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 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 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 each
EUR 692.4

B-Raf Inhibitor 1

2599-5 each
EUR 222

PIM-1 Inhibitor 2

A4519-10 10 mg
EUR 268.8
Description: Potent Pim-1 kinase inhibitor (Ki = 91 nM).

PIM-1 Inhibitor 2

A4519-5 5 mg
EUR 205.2
Description: Potent Pim-1 kinase inhibitor (Ki = 91 nM).

c-Met inhibitor 1

HY-15735 5mg
EUR 424.8

SEC inhibitor KL-1

HY-122720 10mM/1mL
EUR 280.8

GSK-3 inhibitor 1

HY-13973A 100mg
EUR 3531.6

B-Raf inhibitor 1

HY-14177 5mg
EUR 224.4

IRAK-1/4 Inhibitor

9578-25 each
EUR 705.6

IRAK-1/4 Inhibitor

9578-5 each
EUR 222

DGAT-1 inhibitor 2

HY-50670 10mM/1mL
EUR 387.6

Aurora B inhibitor 1

HY-U00304 20mg
EUR 8407.2

PIN1 inhibitor API-1

HY-116716 100mg
EUR 3916.8

Ketohexokinase inhibitor 1

HY-U00461 25mg
EUR 3642

TAO Kinase inhibitor 1

HY-112136 50mg
EUR 955.2

HDACs/mTOR Inhibitor 1

HY-114414 10mg
EUR 1093.2

C-1 Inhibitor Antibody

abx022827-10ml 10 ml
EUR 427.2

TAK1/MAP4K2 inhibitor 1

HY-77251 50mg
EUR 1822.8

anti-HGFA Inhibitor 1

YF-PA14757 50 ul
EUR 435.6
Description: Mouse polyclonal to HGFA Inhibitor 1

PD-1/PD-L1 Inhibitor 1

B1213-25 each
EUR 679.2

PD-1/PD-L1 inhibitor 1

B6172-25 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 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.

Herpes Virus Inhibitor 1

5-01301 4 x 5mg Ask for price

HGFA Inhibitor 1 Antibody

DF13954 100ul
EUR 420

HIV-1 integrase inhibitor

A3461-10 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

A3461-100 100 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 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 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.

Sodium Channel inhibitor 1

HY-15736 100mg
EUR 2539.2

S63845 MCL 1 inhibitor