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TP1246LACTH (22-39) acetateACTH (2239) acetate,ACTH (22 39) acetate
ACTH (22-39) acetate is a fragment of adrenocorticotropic hormone (ACTH) containing two proline residues at positions 3 and 15 from the N-terminus.
价 格:¥电议型 号:TP1246L产 地:中国大陆
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TN3469AucuparinAucuparin
Aucuparin is a phytoalexin, it shows significant scavenging activity by the ABTS and FRAP assays. Aucuparin exhibits potent inhibitory activity against fMLP-induced superoxide (O(*-)(2)) production by human neutrophils with the IC(50) value of 17.0+/-6.8 microM.
价 格:¥电议型 号:TN3469产 地:中国大陆
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T6546IPA-3inhibit,Inhibitor,IPA-3,p21 activated kinases,PAK
IPA-3 is a selective non-ATP competitive Pak1 inhibitor with IC50 of 2.5 μM, no inhibition to group II PAKs (PAKs 4-6).
价 格:¥电议型 号:T6546产 地:中国大陆
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T9464CYM50358CYM50358,LPL Receptor,Lysophospholipid Receptor,CYM-50358,Inhibitor,CYM 50358,inhibit,S1PR4
N-(4-(aminomethyl)-2,6-dimethylphenyl)-5 is a potent, selective antagonist of the sphingosine-1-phosphate receptor 4 (S1P4). CYM50358 inhibits S1P4?with an IC50?of 25 nM.
价 格:¥电议型 号:T9464产 地:中国大陆
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T8462Enoximoneinhibit,Enoximone,bronchodilatory,CD11b,eosinophils,vasodilating,Phosphodiesterase (PDE),ai
Enoximone is a selective inhibitor of phosphodiesterase III (PDE3), with treatment of congestive heart failure.
价 格:¥电议型 号:T8462产 地:中国大陆
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T9722YTX-465YTX-465,α-synuclein,YTX465,fatty desaturation,Stearoyl-CoA Desaturase (SCD),Inhibitor,YTX 465
YTX-465 is an inhibitor of both stearoyl-CoA desaturase(IC50s = 39 nM) and Ole1 (IC50s = 30.4 μM).
价 格:¥电议型 号:T9722产 地:中国大陆
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T15465HC-070
HC-070 is a TRPC5 and TRPC4 antagonist (IC50 = 9.3 nM and 46 nM).
价 格:¥电议型 号:T15465产 地:中国大陆
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T7646AlloepipregnanoloneAlloepipregnanolone
Alloepipregnanolone is a pregnane with anesthetic, hypnotic, and sedative properties.
价 格:¥电议型 号:T7646产 地:中国大陆
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TP2446LAngiotensin amide acetateAngiotensin amide acetate
Angiotensin amide acetate is a chemical compound.
价 格:¥电议型 号:TP2446L产 地:中国大陆
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TQ0086AF38469inhibit,AF 38469,Neurotensin Receptor,Inhibitor,AF38469
AF38469 is a new, specific and orally bioavailable Sortilin inhibitor (IC50: 330 nM).
价 格:¥电议型 号:TQ0086产 地:中国大陆
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T9460iMDKinhibit,iMDK,midkine,factor,PI3K,NSCLC,growth,Inhibitor,Phosphoinositide 3-kinase,MDK
iMDK quarterhydrate is a potent PI3K inhibitor that inhibits the growth factor MDK (also known as midkine or MK). iMDK quarterhydrate synergistically inhibits non-small cell lung cancer (NSCLC) with MEK inhibitors without harming normal cells and mice.
价 格:¥电议型 号:T9460产 地:中国大陆
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T9846WAY-327157WAY327157,WAY 327157
5-HT3 antagonist 5 is a quinoxalin-2-carboxamide compound which is a 5-HT 3 receptor antagonist. 5-HT3 antagonist 5 exerts antagonism on 5-HT 3 agonist and 2-methyl-5-HT, and exhibits anti-depressant effect in mice [1].
价 格:¥电议型 号:T9846产 地:中国大陆
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T8334CADD522inhibit,MDA-231,Inhibitor,Reactive Oxygen Species,CADD 522,MCF7,MDA-468,breast cancer,CADD522
CADD522 is a potent inhibitor of runt-related transcription factor-2 (RUNX2)-DNA binding with an IC50 of 10 nM, with antitumor activity
价 格:¥电议型 号:T8334产 地:中国大陆
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TP1922L1ELA-11 (human) acetate(1784687-32-6 free base)ELA 11 (human) acetate(1784687 32 6 free base),ELA11 (
ELA-11 (human) acetate high affinity apelin receptor agonist (Ki = 14 nM). Bioactive fragment of ELA-32. Inhibits forskolin-induced cAMP production and stimulates β-arrestin recruitment in vitro.
价 格:¥电议型 号:TP1922L1产 地:中国大陆
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TN1465Cannabigerolcolorectal,5-hydroxytryptamine Receptor,Adrenergic Receptor,ROS,anti-cancer,viability,Ca
Cannabigerol is a high affinity α±2-adrenergic receptor agonist, moderate affinity 5-HT1A receptor antagonist, and low affinity CB1 receptor antagonist ; also binds to the CB2 receptor; it can relieve interocular pressure, which may be of benefit in the treatment of glaucoma.
价 格:¥电议型 号:TN1465产 地:中国大陆
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T12846SB-423562Inhibitor,CaSR,Calcium-sensing receptor,inhibit,SB 423562,SB423562,SB-423562
SB-423562 is a calcium-sensing receptor (CaSR) antagonist and can be used in studies about osteoporosis.
价 格:¥电议型 号:T12846产 地:中国大陆
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T6964ResiquimodHepatitis C virus,R-848,S-28463,R 848,S 28463,Toll-like Receptor (TLR),Inhibitor,Resiquimo
Resiquimod is an imidazoquinoline amine and Toll-like receptor (TLR) agonist with potential immune response modifying activity. Resiquimod exerts its effect through the TLR signaling pathway by binding to and activating TLR7 and 8 mainly on dendritic cells, macrophages, and B-lymphocytes. This induces the nuclear translocation of the transcription activator NF-kB as well as activation of other transcription factors. This may lead to an increase in mRNA levels and subsequent production of cytokin
价 格:¥电议型 号:T6964产 地:中国大陆
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T94636-HYDROXYLAMINOURACIL6 HYDROXYLAMINOURACIL,6HYDROXYLAMINOURACIL
6-HYDROXYLAMINOURACIL is a chemical compound.
价 格:¥电议型 号:T9463产 地:中国大陆
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T74612,4-Diamino-6-hydroxypyrimidinecyclohydrolase-I,VCAM-1,inhibit,GTP,NO Synthase,2,4Diamino6hydroxypyr
2,4-Diamino-6-hydroxypyrimidine (DAHP) is a selective, specific inhibitor of GTP cyclohydrolase I, the rate limiting step for de novo pterin synthesis
价 格:¥电议型 号:T7461产 地:中国大陆