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T38173Propargylcholine；化合物Propargylcholine (bromide)Propargylcholine (bromide)；Propargylcholine (bromide)
Propargylcholine (Propargylcholine (bromide)) is an alkyne-modified choline analog and inhibits choline catabolism at the level of Dgc enzyme-catalyzed dimethylglycine demethylation in Pseudomonas aeruginosa.
价 格：￥电议型 号：T38173产 地：中国大陆
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T3812(20R)-Ginsenoside Rg3；(20R)-人参皂苷Rg320(R)-Ginsenoside Rg3|||(20R)Ginsenoside Rg3|||20(R)-Propanaxadio
(20R)-Ginsenoside Rg3 (20(R)-Propanaxadiol) is a compound with anti-aging and antifatigue activities.
价 格：￥电议型 号：T3812产 地：中国大陆
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T38086Neohydroxyaspergillic Acid；Neohydroxyaspergillic AcidNeohydroxyaspergillic Acid
Neohydroxyaspergillic acid is a fungal metabolite produced by A. sclerotiorum that has antibiotic and antifungal activities. It inhibits the growth of P. aeruginosa, M. smegmatis, S. aureus, E. coli, K. pneumoniae, B. mycoides, and B. subtilis bacteria (MICs = 125-500 μg/ml). Neohydroxyaspergillic acid also inhibits the growth of G. convolute, S. consortiale, P. blakesleeanus, C. globosum, and T. mentagrophytes (MICs = 175-700 μg/ml) but not A. niger, P. notatum, M. verrucaria, or S. cerevisiae
价 格：￥电议型 号：T38086产 地：中国大陆
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T38079DL-Propargylglycine HCl；DL-炔丙基甘氨酸盐酸盐DL-Propargyl Glycine HCl|||DL-Propargyl Glycine hydrochloride；DL
DL-Propargylglycine HCl (DL-Propargyl Glycine HCl) is a potent irreversible inhibitor of cystathionine γ-cleaving enzyme and can be used in the study of heart failure.
价 格：￥电议型 号：T38079产 地：中国大陆
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T38017Nω-Propyl-L-arginine hydrochloride；Nw-Propyl-L-arginine hydrochlorideNω-Propyl-L-arginine hydrochlor
Highly selective and potent inhibitor of nNOS (Ki = 57 nM). Displays 3158-fold and 149-fold selectivity over iNOS and eNOS respectively. Hypotensive in vivo.
价 格：￥电议型 号：T38017产 地：中国大陆
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T37962Paeoniflorgenin；芍药苷元Paeoniflorgenin
Paeoniflorgenin is a deglucosylated metabolite of Paeoniflorin[1].
价 格：￥电议型 号：T37962产 地：中国大陆
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T37870Bz-Nle-Lys-Arg-Arg-AMC；Bz-Nle-Lys-Arg-Arg-AMCBz-Nle-Lys-Arg-Arg-AMC
Substrate for dengue virus NS2B-NS3 and yellow fever virus NS3 protease. The kcat/Km value of Bz-NleKRR-AMC for the dengue virus type 4 (DEN4) enzyme is > 800 fold higher than that of Boc-Gly-Arg-Arg-AMC, a widely used NS3 substrate (kcat = 2.9 s 1, Km = 8.6 μM for DEN4). For yellow fever virus NS3 protease the kcat value was 0.111 s 1, the Km value 14.6 μM.
价 格：￥电议型 号：T37870产 地：中国大陆
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T37858Dehydroergosterol；Dehydroergosterol9,11-dehydro Ergosterol|||DHE；9,11-dehydro Ergosterol|||DHE
Dehydroergosterol is a naturally occurring, fluorescent analog of cholesterol (ex/em = 324/375 nm) that mimics the properties of cholesterol in cell membranes.[1] It is readily bound by cholesterol-binding proteins and has been used for real-time probing of the sterol environment and to elucidate intracellular sterol trafficking in living organisms.[1]
价 格：￥电议型 号：T37858产 地：中国大陆
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T37802Phospho-L-Arginine (lithium salt hydrate)；Phospho-L-Arginine (lithium salt hydrate)Phospho-L-Arginin
Phospho-L-arginine is a phosphorylated form of L-arginine and a highly diffusible, high-energy metabolite and phosphagen involved in energy storage in invertebrates including crustaceans, insects, and Trypanosoma species. In the locust L. migratoria, phospho-L-arginine is found in the flight muscles, where it acts as both a buffer system and shuttle mechanism for high-energy phosphate. Measurement of phospho-L-arginine by 31P-NMR spectroscopy has been used to study invertebrate energy metabolism
价 格：￥电议型 号：T37802产 地：中国大陆
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T37700Org 24598 lithium salt；Org 24598 lithium saltOrg 24598 lithium salt
Org 24598 lithium salt is a GlyT-1 inhibitor of glycine transporter 1. Org 24598 lithium salt inhibits the specific binding of [3H]CHIBA-3007 to rat meninges (Ki=16.9 nM).
价 格：￥电议型 号：T37700产 地：中国大陆
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T37699Org 24598；Org 24598Org 24598|||Org 24598；Org 24598|||Org 24598
Potent and selective inhibitor of the glial glycine transporter GlyT1b (IC50 = 6.9 nM). Displays negligible activity at GlyT-2, adrenoreceptors, dopamine, 5HT receptors and noradrenaline, dopamine, 5HT and GABA transporters (pIC50 in vivo.
价 格：￥电议型 号：T37699产 地：中国大陆
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T3767Polygalacic acid；毛果一枝黄花皂苷元GVirgaureagenin G；Virgaureagenin G|||毛果一枝黄花皂苷元G|||远志酸
Polygalacic acid (Virgaureagenin G)(PA) significantly improves cholinergic system reactivity, as indicated by decreased acetylcholinesterase (AChE) activity, increases choline acetyltransferase (ChAT) activity, and elevates levels of acetylcholine (ACh) in the hippocampus and frontal cortex, PA also significantly ameliorates neuroinflammation and oxidative stress in mice; suggest that PA might exert a significant neuroprotective effect on cognitive impairment, driven in part by the modulation of
价 格：￥电议型 号：T3767产 地：中国大陆
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T376475α-dihydro Levonorgestrel；5α-dihydro Levonorgestrel5α-dihydro Levonorgestrel
5α-dihydro Levonorgestrel is a metabolite of the synthetic progestin levonorgestrel . It lacks in vitro and in vivo estrogenic activity, but induces copulatory behavior in male rats when administered at a dose of 1 mg per animal per day.
价 格：￥电议型 号：T37647产 地：中国大陆
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T37609(rel)-Asperparaline A；Aspergillimide(rel)-Asperparaline A
Aspergillimide is a fungal metabolite originally isolated from A. japonicus.1 It reduces nicotinic acetylcholine receptor (nAChR) peak and slowly-desensitizing amplitudes induced by acetylcholine in silkworm (B. mori) larval neurons (IC50s = 20.2 and 39.6 nM, respectively) but has no effect on chicken α3β4-, α4β2-, and α7-containing nAChRs.2 Dietary administration of aspergillimide A (10 μg/g of diet) induces paralysis in silkworm fourth instar larvae.1 Aspergillimide A (10 and 20 mg/kg) reduces
价 格：￥电议型 号：T37609产 地：中国大陆
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T37577Glycogen Phosphorylase Inhibitor；Glycogen Phosphorylase InhibitorGlycogen Phosphorylase Inhibitor
Glycogen phosphorylase in the liver, muscle, and brain initiate glycogenolysis by releasing glucose-1-phosphate from glycogen. Glycogen phosphorylase inhibitor is a cell-permeable acyl urea first identified as an inhibitor of human liver glycogen phosphorylase (IC50 = 53 nM). It blocks glucagon-induced hepatic glycogenolysis in vivo. Glycogen phosphorylase inhibitor has been used to study glycogen utilization in human liver HepG2 cells, retinal explants, and human T lymphocyte Kit 225 cells.
价 格：￥电议型 号：T37577产 地：中国大陆
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T37504Cathepsin D and E FRET Substrate；Mca-Gly-Lys-Pro-Ile-Leu-Phe-Phe-Arg-Leu-Lys(Dnp)-D-Arg-NH?Cathepsin
Mca-GKPILFFRL-Dpa-r-amide, FRET substrate for cathepsin D and E. Also cleaved by napsin A.
价 格：￥电议型 号：T37504产 地：中国大陆
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T37442Aspergillin PZ；Aspergillin PZAspergillin PZ
Aspergillin PZ is a fungal metabolite originally isolated from A. awamori. It induces morphological deformation of P. oryzae conidia when used at a concentration of 89 nM. Aspergillin PZ is active against S. epidermidis (MIC = 20 μM) but not S. aureus, E. coli, or B. cereus (MICs = >20 μM). It is cytotoxic to HL-60 promyelocytic leukemia cells (IC50 = 56.61 μM) but not THP-1 acute monocytic leukemia or PC3 prostate cancer cells (IC50s = >80 μM).
价 格：￥电议型 号：T37442产 地：中国大陆
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T37222GLS1 Inhibitor；GLS1 InhibitorGLS1 Inhibitor
GLS1 inhibitor is an inhibitor of glutaminase 1 (GLS1; IC50= 0.021 μM).1It inhibits the growth of NCI H1703 non-small cell lung cancer (NSCLC) cellsin vitro(GI50= 0.011 μM). GLS1 inhibitor (100 mg/kg) reduces tumor growth, increases tumor levels of glutamine, and decreases tumor levels of glutamate and aspartate in an NCI H1703 mouse xenograft model.
价 格：￥电议型 号：T37222产 地：中国大陆
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T37054Z-D-Arg-Gly-Arg-pNA . 2 HCl；Z-D-Arg-Gly-Arg-pNA . 2 HClZ-D-Arg-Gly-Arg-pNA . 2 HCl
Z-RGR-pNA is a chromogenic substrate for the determination of factor Xa.
价 格：￥电议型 号：T37054产 地：中国大陆
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T37053Z-(L-Arg)-AMC (hydrochloride)；Z-(L-Arg)-AMC (hydrochloride)Z-(L-Arg)-AMC (hydrochloride)
Z-(L-Arg)-AMC is a fluorogenic substrate for trypsin, cathepsin B, and cathepsin H.1,2Upon enzymatic cleavage by trypsin, cathepsin B, or cathepsin H, 7-amino-4-methylcoumarin (AMC) is released and its fluorescence can be used to quantify trypsin, cathepsin B, and cathepsin H activity. AMC displays excitation/emission maxima of 340-360/440-460 nm, respectively.
价 格：￥电议型 号：T37053产 地：中国大陆
