a6 — TargetMol Chemicals

Cat No.	Product Name	Synonyms	Targets
T5S2204	Sibiricose A6		Antioxidant
	1. Sibiricose A6 displays antidepressant-like action, it may prevent or relieve depression. 2. Sibiricose A6 shows potent antioxidant activity.		Antioxidant
T26629	Angstrom6	A-6,A 6 peptide,A6,A 6,A6 peptide,A-6 peptide	PAI-1
	Angstrom6 (A-6 peptide) is an 8 amino acid peptide derived from single chain urokinase fibrinogen activator (scuPA) that interferes with the uPA/uPAR cascade and abrogates the downstream effects.Angstrom6 has antitumor a...		PAI-1
TP2425	Cucumarioside A6-2
	Cucumarioside A6-2 is a triterpene glycoside.
T125557	Calystegine A6
	Calystegine A6 is a useful organic compound for research related to life sciences and the catalog number is T125557.
T130031	Iturin A6
	Iturin A6 is a useful organic compound for research related to life sciences and the catalog number is T130031.
TQ0076	KIRA6		IRE1
	KIRA6 is an effective inhibitor of IRE1α RNase kinase (IC50: 0.6 μM). It can trigger an apoptotic response.		IRE1
T13047	Synta66		Calcium Channel
	Synta66 is a store-operated calcium entry channel Orai inhibitor, and used for the research of neurological disease.		Calcium Channel
T2418	A66		PI3K
	A66 is a specific and effective p110α inhibitor(IC50=32 nM).		PI3K
T62568	IXA6		IRE1
	IXA6 is a novel IRE1/XBP1s agonist with potential vasoprotective activity that activates IRE1-XBP1s signaling and XBP1s transcriptional response, which can be used to study neurodegenerative diseases such as Parkinson's ...		IRE1
T28786	SJA6017	SJA-6017,Calpain Inhibitor VI,Calpain-In-4,SJA 6017,Calpain Inhibitor 4
	SJA6017 is a inhibitor of calpain-1 (IC50 = 7.5 nM) and calpain-2 ( IC50 = 78 nM). SJA6017 also inhibits cathepsins B (IC50s = 15 nM) and cathepsins L (IC50s = 1.6 nM). SJA6017 reduces apoptotic cell death, preserves spi...
T61815	AL-GDa62
	AL-GDa62, a potential synthetic lethal agent for gastric cancer treatment, demonstrates efficacy with EC50 values of 3.2 μM in MCF10A-WT (wild-type) isogenic mammary epithelial cells and 2 μM in MCF10A-CDH1 -/- cells [1]...
T61393	IAA65
	IAA65 is a potent inhibitor of T-type calcium channels, exhibiting an IC50 value of 18.9 μM, and holds potential for use in epilepsy research [1].
T36833	A6770
	A6770 is an inhibitor of sphingosine-1-phosphate (S1P) lyase.1It induces accumulation of [3H]sphinganine-1-phosphate ([3H]dhS1P), an S1P lyase substrate, in IT-79MTNC3 cells that endogenously express high levels of S1P l...
T26432	A68930	A 68930,A70108,A-68930,A 70108,A-70108
	A 68930 is a dopamine D-1 receptor antagonist. A 68930 inhibits NLRP3 inflammasome activity.
T63116	TXA6101
	TXA6101 is an inhibitor of the bacterial protein FtsZ (filamentous temperature sensitive protein Z). TXA6101 inhibits bacterial division and has an MIC of 1 μg/mL against MRSA isolates expressing either the G193D or G196...
T28467	PSMA617-TCMC TFA	PSMA617-TCMC TFA salt,PSMA617-analog, PSMA617-derivative with TCMC,PSMA-617-TCMC
	PSMA617-TCMC is a derivative of PSMA-617 with structure modification, in which the caroboxy groups in DOTA ring is replaced by TCMC macrocycle. PSMA-617 is a ligand used to make 177Lu-PSMA-617, which is a radioactive mol...
T71351	STAT3-IN-A69
	STAT3-IN-A69 is an inhibitor targeting the DNA-binding domain of STAT3, suppressing tumor growth, metastasis and STAT3 target gene expression in vivo.
T76351	[D-Ala6]-LH-RH
	[D-Ala6]-LH-RH, a Luteinizing-hormone-releasing hormone (LHRH) analogue, functions as a gonadotropin-releasing hormone (GnRH) receptor agonist [1].
T82319	Ginsenoside Ra6	Ginsenoside IV
	Ginsenoside Ra6 (Ginsenoside IV), a panaxadiol-type ginsenoside, is isolated from the roots of ginseng [1].
T83732	Tat-CBD3A6K TFA
	Tat-CBD3A6K, a peptide derivative of the N-type voltage-gated calcium channel Cav2.2 and collapsin response mediator protein 2 (CRMP2) interaction inhibitor Tat-CBD3, has demonstrated efficacy in a rat model of antiretro...