Anti P2Y12 Platelet ADP Receptor antibody produced in rabbitfrom BOC Sciences

RAD51-IN-1

RAD51-IN-1 is a derivative of B02 and a potent inhibitor of RAD51. RAD51-IN-1 can be used for...

Cat# 2101739-18-6, Inquire Ask

MtbHU-IN-1

MtbHU-IN-1 is an inhibitor of Mycobacterium tuberculosis nucleoid-associated protein HU (MtbHU),...

Cat# 59736-84-4, Inquire Ask

HCV-IN-29

HCV-IN-29 is an inhibitor of hepatitis C virus (HCV). (Exacted from patent US8329159B2, compound 1e)

Cat# 1009119-83-8, Inquire Ask

Nampt-IN-3

Nampt-IN-3 simultaneously inhibits nicotinamide phosphoribosyltransferase (NAMPT) and HDAC...

Cat# 2121591-52-2, Inquire Ask

EGFR-IN-5

EGFR-IN-5 is an inhibitor of EGFR with IC50s of 10.4, 1.1, 34 and 7.2 nM for EGFR, EGFRL858R,...

Cat# 2225887-26-1, Inquire Ask

KDM2B-IN-4

KDM2B-IN-4 is a histone demethylase KDM2B inhibitor that can be used in cancer research....

Cat# 1966933-85-6, Inquire Ask

MDRTB-IN-1

MDRTB-IN-1 is an antibiotic and it is against Mycobacterium tuberculosis H37Rv with a MIC90...

Cat# 1973401-05-6, Inquire Ask

EZH2-IN-5

EZH2-IN-5 is a potent inhibitor of EZH2 with IC50s of 1.52 and 4.07 nM for wild-type and mutant...

Cat# 1403258-69-4, Inquire Ask

PRMT5-IN-10

PRMT5-IN-10 has a promising structure-dependent inhibitory effect on the protein...

Cat# 2567564-23-0, Inquire Ask

MYC-IN-2

MYC-IN-2 is a MYC protein-protein inhibitor that can be used in cancer research.

Cat# 2244979-61-9, Inquire Ask

RAD51-IN-3

RAD51-IN-3 is a Rad51 inhibitor extracted from patent WO2019051465A1, compound Example 66A.

Cat# 2301084-99-9, Inquire Ask

IDO-IN-2

IDO-IN-2 is a potent inhibitor of IDO (indoleamine-(2,3)-dioxygenase) with IC50 of 3 nM.

Cat# 1668565-74-9, Inquire Ask

KHK-IN-1

KHK-IN-1, a pyrimidinopyrimidine derivative, is a ketohexokinase inhibitor that could have...

Cat# 1303469-70-6, Inquire Ask

CDK9-IN-7

CDK9-IN-7 is a highly selective and orally active CDK9/cyclin T inhibitor (IC50 = 11 nM), which...

Cat# 2369981-71-3, Inquire Ask

PKR-IN-2

PKR-IN-2 is a pyruvate kinase (PKR) activator. IC50: PKR (R510Q) <100 nM

Cat# 1628428-01-2, Inquire Ask

BMX-IN-1

BMX-IN-1 selectively and irreversibly inhibits BMX (IC50=8nM) that is significant for...

Cat# 1431525-23-3, Inquire Ask

CDK7-IN-1

CDK7-IN-1 is an analog of YKL-5-124 and a CDK7 inhibitor with an IC50 of less than 100 nM....

Cat# 1957203-02-9, Inquire Ask

JAK-IN-15

JAK-IN-15 is an inhibitor of JAK. (Extracted from patent WO2016119700A1, compound 15)

Cat# 1973485-05-0, Inquire Ask

Aβ42-IN-2

Aβ42-IN-2 is a γ-secretase modulator (IC50 = 6.5 nM for Aβ42) used in the study of Alzheimer's...

Cat# 1914989-80-2, Inquire Ask

FAS-IN-1

FAS-IN-1, a diazaspiro derivative, has been found to be a fatty acid synthase inhibitor that...

Cat# 1375105-96-6, Inquire Ask

Bromodomain IN-1

Bromodomain IN-1 is an inhibitor of Bromodomain. (Extracted from patent WO2016069578A1, compound 4)

Cat# 1914120-48-1, Inquire Ask

IRAK4-IN-3

IRAK4-IN-3 is a compound with exceptional potency and selectivity against interleukin-1...

Cat# 2196204-23-4, Inquire Ask

DHODH-IN-9

DHODH-IN-9, an azine-bearing analogue, is a human dihydroorotate dehydrogenase inhibitor with...

Cat# 1644156-41-1, Inquire Ask

SIRT-IN-3

SIRT-IN-3 is a novel SIRT inhibitor. SIRTs have been suggested to be associated with certain...

Cat# 1211-19-4, Inquire Ask

RET-IN-5

RET-IN-5 is a potent RET inhibitor with an IC50s of 0.4 nM and 135.1 nM for RET and VEGFR2, respectively.

Cat# 2725770-20-5, Inquire Ask

USP7-IN-1

USP7-IN-1 is a novel selective and reversible inhibitor of USP7 with IC50 of 33 uM; less or no...

Cat# 1381291-36-6, Inquire Ask

CD73-IN-5

CD73-IN-5 is a potent and selective non-nucleotide small molecule CD73 inhibitor with an IC50 of 19 nM.

Cat# 2412019-99-7, Inquire Ask

JAK3-IN-6

JAK3-IN-6 is a potent and highly selective JAK3 inhibitor with Ki values of 0.07 nM, 320 nM, 740...

Cat# 1443235-95-7, Inquire Ask

HAT-IN-1

HAT-IN-1 is an inhibitor of HAT, used in cancer research.

Cat# 1889281-94-0, Inquire Ask

IDO-IN-6

A potent human IDO inhibitor with IC50 of <1 μM.

Cat# 1402837-76-6, Inquire Ask

HPK1-IN-17

HPK1-IN-17 is a potent and selective inhibitor of HPK1 extracted from patent WO2019238067A1,...

Cat# 2403600-07-5, Inquire Ask

PERK-IN-4

PERK-IN-4 is a cell-permeable, highly potent EIF2AK3/PERK inhibitor (IC50 = 0.4 nM) that targets...

Cat# 1337531-89-1, Inquire Ask

FD-IN-1

FD-IN-1 is an orally bioavailable and selective inhibitor of factor D (FD) with an IC50 of 12...

Cat# 1646682-14-5, Inquire Ask

LSD1-IN-6

LSD1-IN-6, a potent and reversible lysine-specific demethylase 1 (LSD1) inhibitor (IC50 = 123...

Cat# 2035912-43-5, Inquire Ask

HPK1-IN-11

HPK1-IN-11 is a potent inhibitor of HPK1 extracted from patent WO2021213317A1, compound 2....

Cat# 2734167-68-9, Inquire Ask

PARP1-IN-7

PARP1-IN-7 is an inhibitor of poly(ADP-ribose) polymerase-1 (PARP1) and it is used as an...

Cat# 2084112-75-2, Inquire Ask

PI3K-IN-2

PI3K-IN-2 is a potent and orally active PI3Kβ/δ inhibitor with excellent selectivity versus...

Cat# 1403458-28-5, Inquire Ask

KDM4-IN-2

KDM4-IN-2 is a potent and selective dual inhibitor of KDM4/KDM5 with Kis of 4 and 7 nM for KDM4A...

Cat# 2369607-62-3, Inquire Ask

Cdc7-IN-5

Cdc7-IN-5, a potent inhibitor of Cdc7 kinase, is a serine-threonine protein kinase enzyme that...

Cat# 1402057-86-6, Inquire Ask

USP7-IN-3

USP7-IN-3 is a potent and selective allosteric inhibitor of ubiquitin-specific protease 7 (USP7).

Cat# 2202738-42-7, Inquire Ask

CXCR2-IN-1

CXCR2-IN-1 is a CXCR2 antagonist (pIC50 = 9.3) with favorable central nervous system penetration...

Cat# 1873376-49-8, Inquire Ask

USP7-IN-5

USP7-IN-5 is a potent ubiquitin specific protease 7 (USP7) inhibitor with an IC50 of 49.9 nM....

Cat# 2166599-74-0, Inquire Ask

PRMT5-IN-9

PRMT5-IN-9 is a PRMT5 inhibitor used in the treatment of cancer, with an IC50 of 0.01 μM.

Cat# 2691869-52-8, Inquire Ask

RET-IN-4

RET-IN-4 is a potent, selective and orally active RET inhibitor with IC50s of 1.29 nM, 1.97 nM,...

Cat# 2436473-55-9, Inquire Ask

DUBs-IN-1

DUBs-IN-1 is a potent deubiquitinase enzyme inhibitor for USP7/USP8.

Cat# 924296-18-4, Inquire Ask

HPK1-IN-10

HPK1-IN-10 is a potent inhibitor of HPK1 extracted from patent WO2021213317A1, compound 103....

Cat# 2734168-69-3, Inquire Ask

PERK-IN-2

PERK-IN-2 is a potent inhibitor of PERK (IC50 of 0.2 nM).

Cat# 1337531-83-5, Inquire Ask

PRMT5-IN-3

PRMT5-IN-3 is an inhibitor of PRMT5, which has a synthetic lethal effect on tumor cells, but...

Cat# 2159123-14-3, Inquire Ask

ERK-IN-3

ERK-IN-3 is a potent and orally active ERK inhibitor that can be used in cancer research caused...

Cat# 2055597-12-9, Inquire Ask

CDK9-IN-6

CDK9-IN-6, one of the CDK9 inhibitors, probably have potential activity in influencing cell...

Cat# 1391855-95-0, Inquire Ask

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