h7 — TargetMol Chemicals

Cat No.	Product Name	Synonyms	Targets
T82246	H7
	H7 is a second near-infrared (NIR-II) fluorophore [1].
T7501	Iso-H7 dihydrochloride		PKC
	Iso-H7 dihydrochloride is a less potent inhibitor of phosphokinase C than H-7.		PKC
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
T81845	Maximin H7
	Maximin H7, an antimicrobial peptide, originates from the toad Bombina maxima [1].
T80357	Bombinin H7
	Bombinin H7, an antimicrobial peptide originating from the skin secretions of Bombina, exhibits bactericidal activity against Bacillus megaterium Bm11 at a lethal concentration of 25.2 μM [1].
T6960	PU-H71		HSP
	PU-H71 is an effective selective HSP90 inhibitor with an IC50 of 51 nM.		HSP
T12870	SCH79797 dihydrochloride		Apoptosis , Others , Protease-activated Receptor
	SCH79797 dihydrochloride is an effective and selective antagonist of protease activated receptor 1 (PAR1) with an IC50 of 70 nM and a Ki of 35 nM. SCH79797 dihydrochloride has antiproliferative and pro-apoptotic effects.		Apoptosis , Others , Protease-activated Receptor
T3599	BFH772	BFH-722	VEGFR
	BFH772, a structure analogue of BAW2881, is a potent and selective VEGF inhibitor. BFH772 is highly effective at targeting VEGFR2 kinase with an IC50 value of 3 nM. BFH772 inhibits the ligand induced autophosphorylation ...		VEGFR
T6960L	PU-H71 HCl	PU-H71 HCl(873436-91-0 Free base),Zelavespib HCl	HSP , DNA/RNA Synthesis
	PU-H71 HCl (Zelavespib HCl) is a novel Hsp90 inhibitor, a novel purine-based analog, and a radiosensitizer that may be a promising agent for CIRT. PU-H71 HCL shows antitumor activity in many preclinical models of maligna...		HSP , DNA/RNA Synthesis
T6066	SCH772984		ERK , MEK
	SCH 772984 is a potent inhibitor of ERK1/ERK2 (IC50: 4/1 nM) and has only weak inhibitory for other 300 tested kinases.		ERK , MEK
T5635	CH7057288		Trk receptor
	CH7057288 is an effective and selective TRK inhibitor with an IC50 value of 1.1 nM, 7.8 nM and 5.1 nM for TRKA, TRKB and TRKC, respectively.		Trk receptor
T15658	KH7		cAMP , AChR
	KH7 is a soluble inhibitor of adenylyl cyclase (sAC)-specific. It has IC50s of 3-10 μM toward both recombinant purified human sACt protein and heterologously expressed sACt in cellular assays. KH7 is also a cAMP inhibito...		cAMP , AChR
T23338	SCH772984 TFA (942183-80-4 free base)	SCH772984 TFA	Others
	ERK1/2 inhibitor		Others
T64714	10× TBS (PH7.4)
	10× TBS (PH7.4) is a reagent and has a wide range of applications in life science related research.
T35334	CH7233163		EGFR
	CH7233163 is a useful organic compound for research related to life sciences and the catalog number is T35334.		EGFR
TN1687	Ginsenoside Rh7		Others
	Ginsenoside Rh7 is a natural product		Others
T69513	(–)-IHCH7041
	(–)-IHCH7041 is a optical rotation negative isomer of IHCH7041. (–)-IHCH7041 is a DRD2 partial agonist. (–)-IHCH7041 showed EC50 = 1.38 nM in Gαi1–γ9 dissociation and 2.75 nM in β-arrestin2 recruitment. (–)-IHCH7041...
T27523	H77-77	H77/77
	H77-77, a monoamine oxidase (MAO) inhibitor, produces a pronounced protection against phenelzine within the serotonergic and noradrenergic neurons in rats.
T28734	SCH79797	SCH 79797,SCH-79797
	SCH-79797 is a potent and selective PAR1 antagonist.
T71247	PU-H71 hydrate
	PU-H71 hydrate is a potent inhibitor of heat shock protein 90 (Hsp90).