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Search Results for " INH "

ターゲット

CFTR Autophagy

1148

阻害剤

天然化合物

リコンビナントタンパク質

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TargetMolキット

カタログ番号	製品名	別名	ターゲット
T2355	CFTR(inh)-172	CFTRinh 172,CFTR Inhibitor-172,CFTRinh-172,CFTRinh172	CFTR , Autophagy
	CFTR(inh)-172 (CFTR Inhibitor-172) is a voltage-independent, selective CFTR inhibitor.		CFTR , Autophagy
T35883	RNF5 inhibitor inh-02	RNF5 inhibitor inh-02
	RNF5 inhibitor inh-02, a potent E3 ubiquitin ligase RNF5/RMA1 inhibitor, demonstrates significant efficacy in rescuing F508del-CFTR with an EC50 of 2.2 uM in bronchial epithelial cells homozygous for the F508del mutation...
T24846	T16A(inh)-C01	T16A(inh) C01
	T16A(inh)-C01 is the Ca(2+)-activated Cl(-) Channel, Ano1 class C inhibitor.
T24847	T16A(inh)-D01	T16A(inh) D01,T16Ainh-D01,T16AinhD01,T16A(inh)D01,T16Ainh D01
	T16A(inh)-D01 is the Ca(2+)-activated Cl(-) Channel, Ano1 class D inhibitor.
T24845	T16A(inh)-B01	T16Ainh-B01,T16A(inh)B01,T16AinhB01,T16Ainh B01
	T16A(inh)-B01 is the Ca(2+)-activated Cl(-) Channel, Ano1 class B inhibitor.
T71615	INH-13
	INH-13 is a Aurora inhibitor.
T0972	Isoniazid	INH,Isonicotinic acid hydrazide,Isonicotinic hydrazide	Mitophagy , Dehydrogenase , CAT , Antibacterial , Autophagy
	Isoniazid (Isonicotinic hydrazide) is an antibacterial agent used primarily as a tuberculostatic.		Mitophagy , Dehydrogenase , CAT , Antibacterial , Autophagy
T6180	INH6		Apoptosis , Microtubule Associated
	INH6, an effective Hec1 inhibitor, selectively disrupts the Hec1/Nek2 interaction and induces chromosome mis-alignment.		Apoptosis , Microtubule Associated
T11657	INH154		Others
	INH154 is a highly potent inhibitor for Nek2 and Hec1 binding (INH), with IC50s of 120 nM and 200 nM for INH in MB468 and Hela cells.		Others
T2502	INH1	IBT13131	Apoptosis , Microtubule Associated
	INH1 (IBT13131) is a cell-permeable Hec1 inhibitor that specifically disrupts the Hec1/Nek2 interaction.		Apoptosis , Microtubule Associated
T5209	INH14		IκB/IKK
	INH14 is a novel inhibitor of the IKKα/β-dependent TLR inflammatory response (IC50s: 8.97/3.59 μM for IKKα/IKKβ).		IκB/IKK
T29081	UTA1inh-C1	UTA1-inh-C1,UTA1(inh)-C1
	UTA1inh-C1 is a novel inhibitor of kidney urea transporter UT-A1.
T29080	UTA1inh-B1	UTA1(inh)-B1,UTA1inhB1
	UTA1inh-B1 is a novel inhibitor of kidney urea transporter UT-A1.
T29079	UTA1inh-A1	UTA1-inh-A1,UTA1(inh)-A1
	UTA1inh-A1 is a novel inhibitor of kidney urea transporter UT-A1.
T29082	UTA1inh-D1	UTA1-inh-D1,UTA1inh D1,UTA1(inh)-D1,UTA1inhD1
	UTA1inh-D1 is a novel inhibitor of kidney urea transporter UT-A1 .
T81024	Tefibazumab	INH-H 2002
	Tefibazumab, a humanized IgG1κ monoclonal antibody, targets and binds to clumping factor A, an adhesion protein expressed on the surface of Staphylococcus aureus, and is under investigation for the treatment of serious S...
T71613	MK-8712
	MK-8712 is a monobactam beta-lactamase inhibitor.
T2602	Barasertib-HQPA	1H-Pyrazole-3-acetamide,Barasertib,AZD1152-HQPA,AZD2811,AZD1152-HQPA\|AZD2811	Apoptosis , Aurora Kinase
	Barasertib-HQPA (AZD2811) is a highly selective Aurora B inhibitor (IC50: 0.37 nM) and demonstrates ~3,700-fold greater selectivity than Aurora A.		Apoptosis , Aurora Kinase
T22831	Protein kinase inhibitor H-7 dihydrochloride	H-7 dihydrochloride	PKC
	Protein kinase inhibitor H-7 dihydrochloride(H-7 dihydrochloride) is a potent protein kinase C (PKC) inhibitor. Protein kinase inhibitor H-7 dihydrochloride (100 μM) significantly inhibits TPA (skin tumor promoter, 12-O-...		PKC
T22195	CBFβ Inhibitor	5-Ethyl-4-(4-methoxy-phenyl)-thiazol-2-ylamine	DNA/RNA Synthesis
	CBFβ Inhibitor (5-Ethyl-4-(4-methoxy-phenyl)-thiazol-2-ylamine) is a cell-permeable CBFβ inhibitor and inhibits its association with Runx1.		DNA/RNA Synthesis
T1804	HPGDS inhibitor 1	HPGDS-inhibitor-1	PGE Synthase
	HPGDS inhibitor 1 is a novel and selective inhibitor for Hematopoietic Prostaglandin D Synthase (HPGDS) with an IC50 Value of 0.7 nM.		PGE Synthase
T6335	Tie2 kinase inhibitor 1	Tie2 kinase inhibitor	Tie-2
	Tie2 kinase inhibitor 1 (Tie2 kinase inhibitor), an optimized compound of SB-203580, is selective to Tie2 with IC50 of 0.25 μM, which is 200-fold more effective than p38.		Tie-2
T3593	Src Inhibitor 1	Src Kinase Inhibitor 1,Src-l1	Src
	Src Inhibitor 1 (Src Kinase Inhibitor 1) is a potent and selective dual site Src tyrosine kinase inhibitor.		Src
TP1015	NFAT Inhibitor	VIVIT peptide	Others
	NFAT Inhibitor (VIVIT peptide) is a cell-permeable compound that selectively inhibits calcineurin-mediated dephosphorylation of NFAT.		Others
T6409	ALK kinase inhibitor-1	SAR348830	Others
	SAR348830 is an ALK inhibitor, targeting anaplastic lymphoma kinase.		Others
T15654	Ketohexokinase inhibitor 1	PF-06835919	Others
	Ketohexokinase inhibitor 1 is a ketohexokinase inhibitor (IC50s: 8.4 nM and 66 nM for KHK-C and KHK-A, respectively).		Others
TP2310	Autocamtide-2-related inhibitory peptide		CaMK , Autophagy
	Autocamtide-2-related inhibitory peptide is a highly specific and potent inhibitor of CaMKII with an IC50 of 40 nM.		CaMK , Autophagy
T83627	Pim-1 kinase inhibitor 8		Pim , PKC
	Pim-1 kinase inhibitor 8 is a potent Pim-1 kinase inhibitor with anticancer activity and can effectively inhibit cell migration.Pim-1 kinase inhibitor 8 is cytotoxic to MCF-7 and HepG2 cells, and is a candidate compound ...		Pim , PKC
T50103	NFAT Inhibitor-2		Others
	NFAT Inhibitor-2 is a compound used as a molecular building block.		Others
T5831	Selective PI3Kδ Inhibitor 1		PI3K
	Selective PI3Kδ Inhibitor 1 is a PI3Kδ Inhibitor( IC50 = 0.9 nM).		PI3K
T22043	BCATc Inhibitor 2		Others
	BCATc Inhibitor 2 exhibited an IC50 of 0.8 microM in the hBCATc assays; it is an active and selective inhibitor. BCATc Inhibitor 2 also blocked calcium influx into neuronal cells following inhibition of glutamate uptake,...		Others
T9044	SORT-PGRN interaction inhibitor 1		Neurotensin Receptor
	SORT-PGRN interaction inhibitor 1 is a potent sortilin-progranulin interaction inhibitor(IC50 of 2 μM).		Neurotensin Receptor
T9631	IRAK-4 protein kinase inhibitor 2		IRAK
	IRAK-4 protein kinase inhibitor 2 is a potent interleukin-1 receptor-associated kinase-4 (IRAK-4) inhibitor(IC50 = 4 μM).		IRAK
T60742	HIV-1 integrase inhibitor 8		HIV Protease
	HIV-1 integrase inhibitor 8 is an inhibitor of HIV-1 integrase. Integration is a required step in HIV replication [1].		HIV Protease
T6015	Cathepsin Inhibitor 1		Cysteine Protease
	Cathepsin Inhibitor 1 is an inhibitor of Cathepsin (L, L2, S, K, B) with pIC50 of 7.9, 6.7, 6.0, 5.5 and 5.2, respectively.		Cysteine Protease
T9725	GSK-3β inhibitor 10		Others
	GSK-3β inhibitor 10 has skin-whitening, anti-oxidizing and PPAR activities.		Others
T67899	Topoisomerase II inhibitor 13		Topoisomerase
	Topoisomerase II inhibitor 13 inhibits topoisomerase II (Topo II) that shows strong anti-proliferation activity against HL-60/MX2 cancer cells derived from HL-60 against Topo II toxicity.		Topoisomerase
T9939	JMJD6 inhibitor WL12	2H-1-Benzopyran-2-one, 3-(3H-imidazo[4,5-c]pyridin-2-yl)-6-methyl-,ZINC6733033	Others
	JMJD6 inhibitor WL12 (ZINC6733033) is a first-in-class JMJD6 inhibitor and was shown to be able to suppress JMJD6-dependent cancer cell proliferation including cervical and liver cancer cells, providing a small-molecule ...		Others
T2705	Mutant EGFR inhibitor		EGFR
	Mutant EGFR inhibitor is a selective and potent Mutated EGFR inhibitor, inhibits L858R activating mutant, the Exonl9 deletion activating mutant and the T790M resistance mutant.		EGFR
T37048	MMP-3 Inhibitor		MMP
	MMP-3 Inhibitor is a peptide matrix metalloproteinase-3 (MMP-3) inhibitor with a Ki value of 95 nM.MMP-3 inhibitor has anticancer and antitumor activity.		MMP
T13059	T16Ainh-A01		Chloride channel
	T16Ainh-A01 is a potent inhibitor of TMEM16A Chloride channel, inhibiting TMEM16A-mediated chloride currents (IC50 of 1 µM),and functions as a calcium-activated chloride channel (CaCC).		Chloride channel
T67767	HIF-1 inhibitor-4	HIF-1 inhibitor-4	HIF
	HIF-1 inhibitor-4 (HIF-1 inhibitor-4) is a HIF-1 inhibitor with IC50 of 560 nM. HIF-1 inhibitor-4 reduces the HIF-1α protein level without affecting its mRNA level.		HIF
T60358	SEH inhibitor-7		Epoxide Hydrolase
	sEH inhibitor-7 is a soluble epoxide hydrolase (sEH) inhibitor that inhibits sEH in human and mouse with IC 50 s of 6.2 μM and 0.15 μM, respectively. sEH inhibitor-7 is associated with anti-inflammatory active molecules.		Epoxide Hydrolase
T9393	(E)-Akt inhibitor-IV	(E)-AKTIV,CS-1992	Akt
	(E)-Akt inhibitor-IV ((E)-AKTIV) ((E)-AKTIV) is an inhibitor of PI3K-Akt.		Akt
T9713	δ-secretase inhibitor 11		Beta Amyloid , Caspase
	δ-secretase inhibitor 11 is an inhibitor of δ-secretase and can be used as a lead compound for translational development of AD treatment.		Beta Amyloid , Caspase
T61318	BRD4 Inhibitor-20		Epigenetic Reader Domain
	BRD4 Inhibitor-20 is a potent bromodomain protein 4 (BRD4) inhibitor with oral activity. BRD4 Inhibitor-20 has antiproliferative activity in cancer cell lines and is used in studies of various cancers, such as colon canc...		Epigenetic Reader Domain
T11190	EMT inhibitor-1		Wnt/beta-catenin
	EMT inhibitor-1 is an inhibitor of Hippo, Wnt signaling and TGF- macrophages (TGF-) with antitumor activity.		Wnt/beta-catenin
T11279	FGFR1/DDR2 inhibitor 1		Discoidin Domain Receptor (DDR) , FGFR , Others
	FGFR1/DDR2 inhibitor 1 is an inhibitor of discoindin domain receptor 2 (DDR2) and fibroblast growth factor receptor 1 (FGFR1), with IC50 values of 31.1 nM, 108.4 nM and 3.2 nM for FGFR1, KG-1, and DDR2, respectively.		Discoidin Domain Receptor (DDR) , FGFR , Others
T21512	MMP-2/MMP-9 Inhibitor I		MMP
	MMP-2/MMP-9-IN-1 is a potent, highly selective and orally bioavailable inhibitor of type IV collagenases (MMP-9 and MMP-2) with an IC50 of 0.24 and 0.3 1 μM for MMP-9 and MMP-2, respectively. activity, which can be used ...		MMP
T17192	Ubiquitin Isopeptidase Inhibitor I, G5	NSC144303	Apoptosis
	Ubiquitin Isopeptidase Inhibitor I, G5 is a caspase-independent inducer of cell necrosis that induces cell death via the death receptor pathway (IC50 of 1.76 and 1.6 μM in E1A and E1A/C9DN cells, respectively).		Apoptosis

Compounds

CFTR(inh)-172

T2355

Synonym: CFTRinh 172,CFTR Inhibitor-172,CFTRinh-172,CFTRinh172

Target: CFTR, Autophagy

RNF5 inhibitor inh-02

T35883

Synonym: RNF5 inhibitor inh-02

Target:

T16A(inh)-C01

T24846

Synonym: T16A(inh) C01

Target:

T16A(inh)-D01

T24847

Synonym: T16A(inh) D01,T16Ainh-D01,T16AinhD01,T16A(inh)D01,T16Ainh D01

Target:

T16A(inh)-B01

T24845

Synonym: T16Ainh-B01,T16A(inh)B01,T16AinhB01,T16Ainh B01

INH-13

Synonym: INH,Isonicotinic acid hydrazide,Isonicotinic hydrazide

Target: Mitophagy, Dehydrogenase, CAT, Antibacterial, Autophagy

INH6

T6180

Synonym:

Target: Apoptosis, Microtubule Associated

INH154

INH1

Target: Apoptosis, Microtubule Associated

INH14

Synonym: UTA1-inh-C1,UTA1(inh)-C1

Target:

UTA1inh-B1

T29080

Synonym: UTA1(inh)-B1,UTA1inhB1

Target:

UTA1inh-A1

T29079

Synonym: UTA1-inh-A1,UTA1(inh)-A1

Target:

UTA1inh-D1

T29082

Synonym: UTA1-inh-D1,UTA1inh D1,UTA1(inh)-D1,UTA1inhD1

Target:

Tefibazumab

T81024

Synonym: INH-H 2002

Synonym: 1H-Pyrazole-3-acetamide,Barasertib,AZD1152-HQPA,AZD2811,AZD1152-HQPA|AZD2811

Target: Apoptosis, Aurora Kinase

Protein kinase inhibitor H-7 dihydrochloride

T22831

Synonym: H-7 dihydrochloride

Target: PKC

CBFβ Inhibitor

T22195

Synonym: 5-Ethyl-4-(4-methoxy-phenyl)-thiazol-2-ylamine

Target: DNA/RNA Synthesis

HPGDS inhibitor 1

T1804

Synonym: HPGDS-inhibitor-1

Target: PGE Synthase

Tie2 kinase inhibitor 1

T6335

Synonym: Tie2 kinase inhibitor

Target: Tie-2

Src Inhibitor 1

T3593

Synonym: Src Kinase Inhibitor 1,Src-l1

Target: Src

NFAT Inhibitor

TP1015

Synonym: VIVIT peptide

Target: Others

ALK kinase inhibitor-1

T6409

Synonym: SAR348830

Target: Others

Ketohexokinase inhibitor 1

T15654

Synonym: PF-06835919

Target: Others

Autocamtide-2-related inhibitory peptide

TP2310

Synonym:

Target: CaMK, Autophagy

Pim-1 kinase inhibitor 8

Selective PI3Kδ Inhibitor 1

SORT-PGRN interaction inhibitor 1

T9044

Synonym:

Target: Neurotensin Receptor

IRAK-4 protein kinase inhibitor 2

T9631

Synonym:

Target: IRAK

HIV-1 integrase inhibitor 8

T60742

Synonym:

Target: HIV Protease

Cathepsin Inhibitor 1

T6015

Synonym:

Target: Cysteine Protease

GSK-3β inhibitor 10

T9725

Synonym:

Target: Others

Topoisomerase II inhibitor 13

T67899

Synonym:

Target: Topoisomerase

JMJD6 inhibitor WL12

T9939

Synonym: 2H-1-Benzopyran-2-one, 3-(3H-imidazo[4,5-c]pyridin-2-yl)-6-methyl-,ZINC6733033

Target: Others

Mutant EGFR inhibitor

Target: Chloride channel

HIF-1 inhibitor-4

T67767

Synonym: HIF-1 inhibitor-4

Target: Epoxide Hydrolase

(E)-Akt inhibitor-IV

T9393

Synonym: (E)-AKTIV,CS-1992

Target: Akt

δ-secretase inhibitor 11

T9713

Synonym:

Target: Beta Amyloid, Caspase

BRD4 Inhibitor-20

T61318

Synonym:

Target: Epigenetic Reader Domain

EMT inhibitor-1

T11190

Synonym:

Target: Wnt/beta-catenin

FGFR1/DDR2 inhibitor 1

T11279

Synonym:

Target: Discoidin Domain Receptor (DDR), FGFR, Others

MMP-2/MMP-9 Inhibitor I

T21512

Synonym:

Target: MMP

Ubiquitin Isopeptidase Inhibitor I, G5

T17192

Synonym: NSC144303

Target: Apoptosis

カタログ番号	製品名	別名	ターゲット
T35782	Swinholide A	MK-7684	Antifungal
	Swinholide A is a polyketone compound that can be extracted from sponges and binds to actin to dimerize actin with Kd of about 50 nM. Swinholide A is a cytotoxin that stabilizes actin dimers and severs actin filaments. S...		Antifungal
TN1848	Kuwanon E		AChR
	Kuwanon E inhibited cholinesterase enzyme in a dose-dependent manner with K i values ranging between 3.1 and 37.5 μM and between 1.7 and 19.1 μM against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzyme...		AChR

天然物製品

Recombinant Proteins

Species：

Expression System：

Tag：

カタログ番号	製品名	Species	Expression System
TMPJ-01064	Serpin G1 Protein, Mouse, Recombinant (His)	Mouse	HEK293 Cells
	SERPIN G1 is a member of the serpin family, The C-terminal serpin domain is similar to other serpins, and this part of C1-INH provides the inhibitory activity. SERPIN G1 is involved in the inhibition of the complement sy...
TMPJ-00502	Serpin G1 Protein, Human, Recombinant (His)	Human	HEK293 Cells
	As protease inhibitors, serpins have an array of functions including regulating blood clotting, the complement pathway, extracellular matrix remodeling, and cell motility. Serpin G1 is a serine protease inhibitor protein...
TMPY-04815	C1 inhibitor Protein, Rat, Recombinant (His)	Rat	HEK293 Cells
	C1 inhibitor Protein, Rat, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 54.7 kDa and the accession number is A6HMR4.
TMPH-01530	INHBA Protein, Human, Recombinant (His & SUMO)	Human	E. coli
	Inhibins and activins inhibit and activate, respectively, the secretion of follitropin by the pituitary gland. Inhibins/activins are involved in regulating a number of diverse functions such as hypothalamic and pituitary...
TMPH-00520	Host-nuclease inhibitor protein gam Protein, Enterobacteria phage lambda, Recombinant (His & Myc)	Escherichia phage lambda	E. coli
	Binds to host RecBCD nuclease and inhibits it thereby protecting the viral DNA against recBCD mediated degradation.
TMPJ-01015	INHBC Protein, Human, Recombinant (C-His)	Human	HEK293 Cells
	Inhibin beta C chain, also known as activin beta-C chain and INHBC, belongs to the TGF-beta family. INHBC forms a homodimeric or heterodimeric through association with alpha and beta subunits, linked by one or more disul...
TMPH-03528	Chemotaxis inhibitory Protein, S. aureus (strain NCTC 8325/PS47), Recombinant (His & Myc)	Staphylococcus aureus	E. coli
	Involved in countering the first line of host defense mechanisms. Specifically inhibits the response of human neutrophils and monocytes to complement anaphylatoxin C5a and formylated peptides, like N-formyl-methionyl-leu...
TMPH-00395	Autolysin Protein, Chlamydomonas reinhardtii, Recombinant (His & SUMO)	Chlamydomonas reinhardtii	E. coli
	Mediates digestion of the cell walls of the 2 mating type gametes during mating as a necessary prelude to cell fusion. This enzyme acts specifically on the framework proteins (inner wall) of the cell wall, cleaving sever...
TMPH-00272	Inhibin alpha chain/INHA Protein, Bovine, Recombinant (His & SUMO)	Bovine	E. coli
	Inhibin alpha chain/INHA Protein, Bovine, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 30.6 kDa and the accession number is P07994.
TMPY-01190	INHBB Protein, Human, Recombinant (His)	Human	HEK293 Cells
	Activin and inhibin are two closely related protein complexes that have almost directly opposite biological effects. The activin and inhibin protein complexes are both dimeric in structure, and, in each complex, the two ...
TMPY-01183	C1 inhibitor Protein, Human, Recombinant (His)	Human	HEK293 Cells
	C1 inhibitor Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 54.3 kDa and the accession number is E9KL26.
TMPH-02787	Muellerian-inhibiting factor/AMH Protein, Mouse, Recombinant (His)	Mouse	P. pastoris (Yeast)
	Muellerian-inhibiting factor/AMH Protein, Mouse, Recombinant (His) is expressed in Yeast.
TMPH-02788	Muellerian-inhibiting factor/AMH Protein, Mouse, Recombinant (E. coli, His)	Mouse	E. coli
	Muellerian-inhibiting factor/AMH Protein, Mouse, Recombinant (E. coli, His) is expressed in E. coli.
TMPH-03529	Chemotaxis inhibitory Protein, S. aureus (strain MRSA252), Recombinant (His)	Staphylococcus aureus	P. pastoris (Yeast)
	Involved in countering the first line of host defense mechanisms. Specifically inhibits the response of human neutrophils and monocytes to complement anaphylatoxin C5a and formylated peptides, like N-formyl-methionyl-leu...
TMPJ-01016	INHBC Protein, Human, Recombinant (N-His)	Human	E. coli
	Inhibins/activins are involved in regulating a number of diverse functions such as hypothalamic and pituitary hormone secretion, gonadal hormone secretion, germ cell development and maturation, erythroid differentiation,...
TMPH-00554	Trypsin inhibitor DE-3 Protein, Erythrina caffra, Recombinant (His)	Erythrina caffra	P. pastoris (Yeast)
	Inhibition of trypsin.
TMPY-05029	INHBE Protein, Human, Recombinant (hFc)	Human	HEK293 Cells
	INHBE (Inhibin Subunit Beta E) is a Protein Coding gene. This gene encodes a member of the TGF-beta (transforming growth factor-beta) superfamily of proteins. The encoded preproprotein is proteolytically processed to gen...

Serpin G1 Protein, Mouse, Recombinant (His)

TMPJ-01064

Species: Mouse

Expression System: HEK293 Cells

Serpin G1 Protein, Human, Recombinant (His)

TMPJ-00502

Species: Human

Expression System: HEK293 Cells

C1 inhibitor Protein, Rat, Recombinant (His)

TMPY-04815

Species: Rat

Expression System: HEK293 Cells

INHBA Protein, Human, Recombinant (His & SUMO)

TMPH-01530

Species: Human

Expression System: E. coli

Host-nuclease inhibitor protein gam Protein, Enterobacteria phage lambda, Recombinant (His & Myc)

TMPH-00520

Species: Escherichia phage lambda

Expression System: E. coli

INHBC Protein, Human, Recombinant (C-His)

TMPJ-01015

Species: Human

Expression System: HEK293 Cells

Chemotaxis inhibitory Protein, S. aureus (strain NCTC 8325/PS47), Recombinant (His & Myc)

TMPH-03528

Species: Staphylococcus aureus

Expression System: E. coli

Autolysin Protein, Chlamydomonas reinhardtii, Recombinant (His & SUMO)

TMPH-00395

Species: Chlamydomonas reinhardtii

Expression System: E. coli

Inhibin alpha chain/INHA Protein, Bovine, Recombinant (His & SUMO)

TMPH-00272

Species: Bovine

Expression System: E. coli

INHBB Protein, Human, Recombinant (His)

TMPY-01190

Species: Human

Expression System: HEK293 Cells

C1 inhibitor Protein, Human, Recombinant (His)

TMPY-01183

Species: Human

Expression System: HEK293 Cells

Muellerian-inhibiting factor/AMH Protein, Mouse, Recombinant (His)

TMPH-02787

Species: Mouse

Expression System: P. pastoris (Yeast)

Muellerian-inhibiting factor/AMH Protein, Mouse, Recombinant (E. coli, His)

TMPH-02788

Species: Mouse

Expression System: E. coli

Chemotaxis inhibitory Protein, S. aureus (strain MRSA252), Recombinant (His)

TMPH-03529

Species: Staphylococcus aureus

Expression System: P. pastoris (Yeast)

INHBC Protein, Human, Recombinant (N-His)

TMPJ-01016

Species: Human

Expression System: E. coli

Trypsin inhibitor DE-3 Protein, Erythrina caffra, Recombinant (His)

TMPH-00554

Species: Erythrina caffra

Expression System: P. pastoris (Yeast)

INHBE Protein, Human, Recombinant (hFc)

TMPY-05029

Species: Human

Expression System: HEK293 Cells

カタログ番号	製品名
L9410	Covalent Inhibitor Library	1920 compounds
	A unique collection of 1920 covalent Inhibitors and other molecules with common warheads like chloroacetyl，2-Chloropropionyl，Acryloyl，sulfonyl fluoride, alkyne，acrylamide, ketocarbonyl，disulfide bond, etc.
L2200	Tyrosine Kinase Inhibitor Library	1016 compounds
	A unique collection of 1016 tyrosine kinase inhibitors for high throughput screening and high content screening for drug discovery in tyrosine kinase related diseases;
L2000	Inhibitor Library	8328 compounds
	A unique collection of 8328 inhibitors for research in cell signaling, high throughput screening (HTS) and high content screening (HCS) for new drugs;
L9400	PPI Inhibitor Library	485 compounds
	A unique collection of 485 PPI-related compounds for drug screening;
L9100	Phosphatase Inhibitor Library	79 compounds
	A collection of 79 phosphatase inhibitors with known activity;
L1100	Protease Inhibitor Library	343 compounds
	A unique collection of 343 protease and proteasome inhibitors for research in chemical genomics, and drug screening;
L2300	Ion Channel Inhibitor Library	931 compounds
	A unique collection of 931 compounds targeting ion channels for research in ion channels-related diseases and ion channel drug discovery;
DO2200	Covalent inhibitors Library	12000 compounds

L1400	MAPK Inhibitor Library	365 compounds
	A unique collection of 365 compounds targeting MAPK signaling for drug discovery in MAPK related diseases;
L1610	FDA-Approved Kinase Inhibitor Library	263 compounds
	A unique collection of 263 kinase inhibitors/regulators for specific targeting of kinases, ready for high-throughput screening and high-content screening.
L3600	Cytokine Inhibitor Library	604 compounds
	A unique collection of 604 compounds targeting cytokine signaling for high throughput screening and high content screening for drug discovery;
L2010	Highly Selective Inhibitor Library	575 compounds

L1600	Kinase Inhibitor Library	2720 compounds
	A unique collection of 2720 kinase inhibitors/regulators for high throughput screening and high content screening for drug discovery in kinase related diseases;
L7600	Chemokine Inhibitor Library	59 compounds
	A unique collection of 59 chemokines or chemokine receptors targeted compounds for high throughput and high content screening;