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T4517L189L189
L189 is a human DNA ligase inhibitor, inhibits hLigI/III/IV (IC50: 5/9/5 μM).
价 格：￥电议型 号：T4517产 地：美洲
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T5189OmadacyclineOmadacycline,Amadacycline,PTK 0796
Omadacycline, a new tetracycline antibiotic, can inhibit the 30s subunit of bacterial ribosome.
价 格：￥电议型 号：T5189产 地：美洲
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T5S1891AcetylaconitineAcetylaconitine,3-Acetylaconitine,Flaconitine
Analgesic activity.
价 格：￥电议型 号：T5S1891产 地：美洲
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T5S1895NorisoboldineNorisoboldine,Laurelliptine,(+)-Laurelliptine
1. Norisoboldine might be a potential therapeutic agent for rheumatoid arthritis, and it functions through protecting joint destruction as well as regulating the abnormal immune responses. 2. Norisoboldine inhibits the macrophage activation and the result
价 格：￥电议型 号：T5S1895产 地：美洲
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T5S1897LinderalactoneLinderalactone
1. Linderalactone showed significant inhibitory effects on superoxide anion generation by human neutrophils in response to fMLP/CB, values of IC5 is 8.48̵µg/mL.
价 格：￥电议型 号：T5S1897产 地：美洲
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T6189PD0325901PD0325901,PD325901,
PD0325901 is a specific and non-ATP-competitive MEK inhibitor (IC50: 0.33 nM).
价 格：￥电议型 号：T6189产 地：美洲
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T6574LumiracoxibLumiracoxib,COX-189,Prexige
Lumiracoxib is a novel, selective COX-2 inhibitor with IC50 and Ki of 0.14 μM and 0.06 μM, exhibits 515-fold selectivity over COX-1. Phase 4.
价 格：￥电议型 号：T6574产 地：美洲
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T83533(R)-Monlunabant；化合物 (R)-Monlunabant(R)-MRI-1891；(R)-MRI-1891
(R)-Monlunabant ((R)-MRI-1891) serves as a CB1 receptor antagonist utilized in obesity and metabolic disease research [1].
价 格：￥电议型 号：T83533产 地：中国大陆
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T83189Acetylthevetin A；化合物 Acetylthevetin AAcetylthevetin A
Acetylthevetin A, a natural product, is isolated from the oleander (Cascabela thevetioides) [1].
价 格：￥电议型 号：T83189产 地：中国大陆
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T82461Epacmarstobart；化合物 EpacmarstobartGS-0189|||FSI-189；GS-0189|||FSI-189
Epacmarstobart (FSI-189; GS-0189) is a chimeric humanized IgG1κ antibody designed to target the mouse Signal Regulatory Protein Alpha (SIRPA).
价 格：￥电议型 号：T82461产 地：中国大陆
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T82189HMGB1-IN-2；化合物 HMGB1-IN-2HMGB1-IN-2
HMGB1-IN-2 (compound 15) is a selective inhibitor of the highly conserved nuclear protein HMGB1, demonstrating no inhibitory effect at an IC50 of 20.2 μM in RAW264.7 cells. At a concentration of 30 μM, HMGB1-IN-2 reduces IL-1β, TNF-α, and caspase-1 p20 levels, and inhibits NF-κB p65 phosphorylation, providing anti-apoptotic effects. In vivo, HMGB1-IN-2 at a dose of 15 mg/kg administered intraperitoneally alleviates kidney injury in a mouse model of septic acute kidney injury. Furthermore, it inh
价 格：￥电议型 号：T82189产 地：中国大陆
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T81899LY836；化合物 LY836LY836
LY836 is an orally active, neuroprotective compound that effectively inhibits the PSD95-nNOS association in cortical neurons. It has potential applications in the study of ischemic stroke [1].
价 格：￥电议型 号：T81899产 地：中国大陆
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T81898Lyciumamide A；化合物 Lyciumamide ALyciumamide A
DPP-IV-IN-5, derived from Lycium barbarum fruits, demonstrates moderate agonistic activity towards peroxisome proliferator-activated receptor (PPARγ), showing EC50 values between 10.09 and 44.26 μM, and exhibits inhibitory activity against dipeptidyl peptidase-4 (DPPIV) with an IC50 of 47.13 μM [1].
价 格：￥电议型 号：T81898产 地：中国大陆
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T81897Lys-Conopressin-G；化合物 Lys-Conopressin-GLys-Conopressin-G
Conopressin-G is a vasotocin-like peptide extracted from the venom of the worm-hunting snail (Conus imperialis) [1] [2].
价 格：￥电议型 号：T81897产 地：中国大陆
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T81896Lysimachigenoside C；化合物 Lysimachigenoside CLysimachigenoside C
Lysimachigenoside C, a triterpene saponin, has been isolated from the plant Lysimachia foenum-graecum Hance [1].
价 格：￥电议型 号：T81896产 地：中国大陆
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T81895Lysophosphatidylcholine C19:0；化合物 Lysophosphatidylcholine C19:01-Nonadecanoyl-2-hydroxy-sn-glycero-3
Lysophosphatidylcholine C19:0 (1-Nonadecanoyl-2-hydroxy-sn-glycero-3-phosphocholine), an acyl chain lipid, enhances IL-1beta secretion [1].
价 格：￥电议型 号：T81895产 地：中国大陆
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T81894Lys-Phe-Glu-Arg-Gln；化合物 Lys-Phe-Glu-Arg-GlnLys-Phe-Glu-Arg-Gln
Lys-Phe-Glu-Arg-Gln promotes cytosolic protein degradation in serum-deprived human diploid fibroblasts [1].
价 格：￥电议型 号：T81894产 地：中国大陆
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T81893M1/M4 muscarinic agonist 2；化合物 M1/M4 muscarinic agonist 2M1/M4 muscarinic agonist 2
Compound 40 is a selective M1/M4 muscarinic antagonist with an IC50 of 19 nM for M1 receptors and 42 nM for M4 receptors [1].
价 格：￥电议型 号：T81893产 地：中国大陆
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T81892M351-110；化合物 M351-110M351-110
M351-110 is an agonist of the V-domain Ig suppressor of T cell activation (VISTA) designed for oncological studies [1].
价 格：￥电议型 号：T81892产 地：中国大陆
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T81891M65；化合物 M65M65
M65 is a PAC1 receptor-specific antagonist that inhibits the secretion of atrial natriuretic peptide (ANP) [1].
价 格：￥电议型 号：T81891产 地：中国大陆
