Phthalic Acid Unlabeled 100 Ug Ml In Mtbefrom BOC Sciences

CDK-IN-2

CDK-IN-2 is a potent and sepecific CDK inhibitor.

Cat# 1269815-17-9, Inquire Ask

Telomerase-IN-1

Telomerase-IN-1 is a Telomerase inhibitor (IC50= 0.19 μM).

Cat# 666859-49-0, Inquire Ask

IDO-IN-5

A potent human IDO inhibitor with IC50 of 1-10 μM.

Cat# 1402837-79-9, Inquire Ask

Mirk-IN-1

Mirk-IN-1, a pyrido[2,3-d]pyrimidine derivative, has been found to be a DYRK1A/B inhibitor and...

Cat# 1386979-55-0, 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

LRRK2-IN-1

LRRK2-IN-1 is a benzodiazepine based derivative and is known as a selective inhibitor of the...

Cat# 1234480-84-2, Inquire Ask

KHK-IN-1

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

Cat# 1303469-70-6, 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

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

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

IDO-IN-6

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

Cat# 1402837-76-6, Inquire Ask

CXCR2-IN-1

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

Cat# 1873376-49-8, Inquire Ask

DUBs-IN-1

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

Cat# 924296-18-4, 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

BRCA1-IN-1

A novel small-molecule-like BRCA1 inhibitor (IC50= 0.53 μM) (Ki= 0.71 μM)

Cat# 1622262-74-1, Inquire Ask

IDO-IN-1

An IDO inhibitor with IC50 of 59 nM, shows activity in Hela cell (IC50=12 nM).

Cat# 914638-30-5, Inquire Ask

Mps1-IN-1

Mps1-IN-1 is a highly potent and selectibe Mpsl inhibitor with IC50 of 367 nM; >1000-fold...

Cat# 1125593-20-5, Inquire Ask

PDE1-IN-2

PDE1-IN-2 is an inhibitor of PDE1 that has IC50 values of 6, 140 and 164 nM for PDE1C, PDE1B and...

Cat# 1904611-63-7, Inquire Ask

KDM4D-IN-1

A novel histone lysine demethylase 4D (KDM4D) inhibitor (IC50= 0.41±0.03 μM)

Cat# 2098902-68-0, Inquire Ask

Nav1.7-IN-2

Nav1.7-IN-2, a voltage-gated sodium channels, could be probably effective in chronic pain...

Cat# 1332295-35-8, Inquire Ask

MPO-IN-28

MPO-IN-28 is a myeloperoxidase (MPO) inhibitor with IC50 of 44 nM.

Cat# 37836-90-1, Inquire Ask

Mps1-IN-2

Small-molecule inhibitor of Mps1 kinase (IC50 values 145 nM) with greater than 1000-fold...

Cat# 1228817-38-6, Inquire Ask

IKKε-IN-1

IKKε-IN-1 is a potent IKKε inhibitor; inhibit the in-situ ΙKΚ ε-mediated phosphorylation of IRF3...

Cat# 1292310-49-6, Inquire Ask

MGAT2-IN-1

An orally active inhibitor of monoacylglycerol acyltransferase (MGAT2) (IC50= 7.8 for human, and...

Cat# 1800025-30-2, Inquire Ask

MD2-IN-1

MD2-IN-1 is an inhibitor of myeloid differentiation protein 2 (MD2) with a KD of 189 μM for...

Cat# 111797-22-9, Inquire Ask

KDM5A-IN-1

KDM5A-IN-1, a pyrrolidine amide compound, is an inhibitor histone demethylases.

Cat# 1905481-36-8, Inquire Ask

CB1-IN-1

CB1-IN-1 is an antagonist of cannabinoid receptor type 1 (CB1R) located in the peripheral...

Cat# 1429239-98-4, Inquire Ask

CaMKII-IN-1

CaMKII-IN-1 is a potent and highly selective CaMKII inhibitor with IC50 of 63 nM; significantly...

Cat# 1208123-85-6, Inquire Ask

STING-IN-2

STING-IN-2 is a covalent STING inhibitor.

Cat# 346691-38-1, Inquire Ask

DGAT1-IN-1

Imidazopyridine and imidazothiazole compounds as inhibitors of diacylglycerol o-acyltransferase...

Cat# 1449779-49-0, Inquire Ask

JNK-IN-7

Covalent modification of IRAK1 by JNK-IN-7 is a possibility and subsequent biochemical kinase...

Cat# 1408064-71-0, Inquire Ask

CDK4-IN-1

CDK 4/6 Inhibitor is a part of a group of compounds that exhibits selective inhibitory...

Cat# 1256963-02-6, Inquire Ask

IRAK4-IN-3

Cat# B2693-336218, 50 mg/unit USD $999 Ask

Ptp1B-In-2

Ptp1B-In-2 is a selective protein tyrosine phosphatase-1B (PTP1B) inhibitor.

Cat# 1919853-46-5, Inquire Ask

PI4KIIIbeta-IN-10

PI4KIIIbeta-IN-10, a potent anti-viral agent, is a highly PI4KIIIβ inhibitor with weak...

Cat# 1881233-39-1, Inquire Ask

FGFR4-IN-1

FGFR4-IN-1 is a potent and selective FGFR4 inhibitor with potential for the treatment of gastric cancer.

Cat# 1708971-72-5, Inquire Ask

MIR96-IN-1

MIR96-IN-1, a benzimidazole derivative, could restrain microRNA-96 biogenesis and also be...

Cat# 1311982-88-3, Inquire Ask

DDR1-IN-1

DDR1-IN-1 is a potent and selective discoidin domain receptor 1 (DDR1) receptor tyrosine kinase...

Cat# 1449685-96-4, Inquire Ask

KDM5-IN-1

KDM5-IN-1 is a potent and selective KDM5 inhibitor with modest cell activity (PC9 H3K4Me3 EC50 = 5.2 μM).

Cat# 1628210-26-3, Inquire Ask

HDAC-IN-1

HDAC-IN-1, an analogue of MC 1568, is a Iia HDACs inhibitor that could probably influence...

Cat# 1239610-44-6, Inquire Ask

Mcl1-IN-2

Mcl1-IN-2, a hydroxyquinoline derivative, is an Mcl-1 inhibitor.

Cat# 292057-76-2, Inquire Ask

PDE1-IN-1

PDE1-IN-1 is a potent PDE1 inhibitor and neuroprotective agent.

Cat# 1160521-50-5, Inquire Ask

PKR-IN-1

Activator of pyruvate kinase isoenzyme M2 (PKM2), an enzyme involved in glycolysis. Since all...

Cat# B0084-463157, 100 mg/unit USD $629 Ask

PI4KIIIbeta-IN-9

PI4KIIIbeta-IN-9, a thiazole derivative, is a selective PI4KIIIβ inhibitor over PI3Kγ...

Cat# 1429624-84-9, Inquire Ask

Irak4-IN-1

Irak4-IN-1 is an inhibitor of interleukin-1 receptor associated kinase 4 (IRAK4).

Cat# B0084-284756, 2 mg/unit USD $239 Ask

STAT5-IN-1

STAT5-IN-1, a cell-permeable nonpeptidic nicotinoyl hydrazone compound, is a selective STAT5...

Cat# B0084-007364, 50 mg/unit USD $399 Ask

ELOVL1-IN-2

ELOVL1-IN-2 is an inhibitor of ELOVL1 (elongation of very-long-chain-fatty acid 1).

Cat# B1370-149624, 50 mg/unit USD $298 Ask

Lyn-IN-1

Bafetinib is a potent and selective dual Bcr-Abl/Lyn inhibitor, but it does not inhibit the...

Cat# 887650-05-7, Inquire Ask

PGS-IN-1

PGS-IN-1 is a potent inhibitor of prostaglandin synthetase (PGS) (IC50= 0.28 μM) and also an...

Cat# 102271-49-8, Inquire Ask

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