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TP1952LPG 106 acetatePG 106 acetate
PG 106 acetate is an effective and selective antagonist of the human melanocortin 3 (hMC3) receptor with an IC50 of 210 nM. PG 106 acetate has no activity with the hMC5 receptor and hMC4 receptors with an EC50 of 9900 nM.
价 格：￥电议型 号：TP1952L产 地：中国大陆
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T9243PFI-90antitumor,Inhibitor,PFI 90,differentiation,PAX3-FOXO1,demethylase,PFI-90,apoptosis,histone,His
PFI-90 is a selective inhibitor of histone demethylase (KDM3B) that inhibits PAX3-FOXO1 action.PFI-90 has the potential for the antitumor activity. PFI-90 induces apoptosis and myogenic differentiation, resulting in the cell death increased.
价 格：￥电议型 号：T9243产 地：中国大陆
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T7393ONO-7300243ONO7300243,inhibit,Inhibitor,ONO 7300243,ONO-7300243,LPL Receptor,Lysophospholipid Recept
ONO-7300243 is an antagonist of lysophosphatidic acid receptor 1 (LPA1; IC50 : 0.16 μM).
价 格：￥电议型 号：T7393产 地：中国大陆
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T7901EmodepsideParasite,Inhibitor,Emodepside,inhibit
Emodepside is an anthelmintic drug that is effective against a number of gastrointestinal nematodes,with broad-spectrum anthelmintic activity.
价 格：￥电议型 号：T7901产 地：中国大陆
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TN1480CephaelineNSC 32944,inhibit,Inhibitor,NSC32944,Ebola,Cephaeline,Filovirus,phenolic,alkaloid,virus,In
Cephaeline was highly active against protected primary CLL cells (relative IC50´s 35nM ) and acted by repressing HIF-1α± and disturbing intracellular redox homeostasis.
价 格：￥电议型 号：TN1480产 地：中国大陆
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T60033SBI993SBI993
SBI993 is an analog of SBI-477 and can be used as a biomarker to confirm the expected action of MondoA target gene expression in vivo. SBI993 reduces muscle TAG levels and hepatic steatosis.
价 格：￥电议型 号：T60033产 地：中国大陆
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T7189AMG9810Transient receptor potential channels,inhibit,Inhibitor,AMG-9810,AMG9810,AMG 9810,TRP Channel
AMG 9810 is a competitive antagonist of capsaicin activation of the vanilloid receptor 1 (TRPV1) (IC50s = 24.5 and 85.6 nM for human and rat TRPV1, respectively).
价 格：￥电议型 号：T7189产 地：中国大陆
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T9493DL-2-AMINOOCTANOIC ACIDDL2AMINOOCTANOIC ACID,DL 2 AMINOOCTANOIC ACID
DL-2-Aminooctanoic acid, also known as a-aminocaprylate or alpha-aminocaprylic acid, belongs to the class of organic compounds known as alpha-amino acids.
价 格：￥电议型 号：T9493产 地：中国大陆
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T9289Phosphonoformic acid trisodium salt hexaPhosphonoformic acid trisodium salt hexa
Phosphonoformic acid trisodium salt hexa is an antiviral drug for the treatment of CMV retinitis.
价 格：￥电议型 号：T9289产 地：中国大陆
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T8838CCI-007CCI 007,MLL-r,CALM-AF10,HOXA9,MEIS1,Apoptosis,CMYC,CCI-007,SET-NUP214,inhibit,Inhibitor,CCI00
CCI 007 is a selective inhibitor of MLL-r, CALM-AF10 and SET-NUP214 leukemia with IC50 of 3.5 uM against MLL-r leukemia cell line PER-485
价 格：￥电议型 号：T8838产 地：中国大陆
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T9298D-ValineDValine,inhibit,Inhibitor,D-Valine,Endogenous Metabolite,D Valine
D-Valine is the enantiomer of L-Valine.
价 格：￥电议型 号：T9298产 地：中国大陆
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TP1238LACTH 1-14 acetate(25696-21-3 free base)ACTH 1 14 acetate(25696 21 3 free base),ACTH 114 acetate(2569
ACTH (1-14) is a fragment of adrenocorticotrophin, which regulates cortisol and androgen production.Adrenocorticotropic hormone (ACTH), also known as corticotropin, is produced and secreted by the anterior pituitary gland. ACTH is an important component of the hypothalamic-pituitary-adrenal axis as a response to biological stress.
价 格：￥电议型 号：TP1238L产 地：中国大陆
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T60094SU 4981
SU 4981 is an inhibitor of VEGFR and a modulator of tyrosine kinase activity.
价 格：￥电议型 号：T60094产 地：中国大陆
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T39752CDK12-IN-2
CDK12-IN-2 is an effective and selective inhibitor of CDK12 with an IC50 of 52 nM, >100 μM, >10 μM and 16 μM for CDK12, CDK2, CDK7, and CDK9. CDK12-IN-2 can be used in studies about the function of CDK12.
价 格：￥电议型 号：T39752产 地：中国大陆
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T6716ValsartanAngiotensin Receptor,Inhibitor,failure,blood,proinflammatory,aorta,CGP-48933,endothelial,cy
Valsartan is a tetrazole derivative and angiotensin II type 1 receptor blocker that is used to treat hypertension.
价 格：￥电议型 号：T6716产 地：中国大陆
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T39214LLXE408 fumarate
LXE408 fumarate is an orally active, non-competitive and kinetoplastid-selective?proteasome?inhibitor. LXE408 fumarate has an?IC50?of 0.04 μM for?L. donovani?proteasome and an?EC50?of 0.04 μM for?L. donovani. LXE408 fumarate has a low propensity to cross the blood brain barrier. LXE408 fumarate has the potential for visceral leishmaniasis (VL) research.
价 格：￥电议型 号：T39214L产 地：中国大陆
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TP2106LUrantide acetate(669089-53-6 free base)Urantide acetate(669089536 free base),Urantide acetate(669089
Urantide acetate is a selective and competitive urotensin-II (UT) receptor antagonist (pKB = 8.3). Blocks hU-II induced contractions in thoracic aorta ex vivo. Exhibits no effect on noradrenaline or endothelin 1-induced contraction or on acetylcholine-induced relaxation. Behaves as a partial agonist in a calcium mobilization assay (in CHO cells expressing hUT receptors).
价 格：￥电议型 号：TP2106L产 地：中国大陆
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T6S0923HypericinHypericin,Dopamine β-monooxygenase,antitumor activity,Antibiotic,antiviral activity,telomer
1. Hypericin has antineoplastic activity. 2. Hypericin has antibiotic and antiviral activities. 3. Hypericin has antidepressive activity through inhibiting monoamine oxidase enzyme. 4. Hypericin inhibits RANKL-mediated osteoclastogenesis via affecting ERK signalling in vitro and suppresses wear particle-induced osteolysis in vivo.
价 格：￥电议型 号：T6S0923产 地：中国大陆
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T9616PD-1/PD-L1-IN-10Lewis,T-lymphocyte,tumor,IFN-γ,Inhibitor,lung,LLC,inhibit,Apoptosis,PD1/PDL1IN10,PD
PD-1/PD-L1-IN-10 is an orally active?PD-1/PD-L1?inhibitor (IC50?of 2.7 nM) with potent anticancer efficacy.
价 格：￥电议型 号：T9616产 地：中国大陆
