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T8126Cefodizime Sodiumspectrum,Gram-negative,tracts,broad,Inhibitor,Antibiotic,urinary,inhibit,Cefodizime
Cefodizime Sodium is a third generation cephalosporin antibiotic, has broad-spectrum activity
价 格：￥电议型 号：T8126产 地：中国大陆
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TP1591LOVA G4 peptide acetate(148274-82-2 free base)OVA G-4 peptide acetate(148274-82-2 free base),OVA G4 p
G4 peptide acetate is a variant of the agonist ovalbumin (OVA) peptide (257-264), SIINFEKL. OVA Peptide is a class I (Kb)-restricted peptide epitope of ovalbumin presented by the class I MHC (major histocompatibility complex) molecule, H-2Kb (class I genes of the mouse MHC).
价 格：￥电议型 号：TP1591L产 地：中国大陆
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TP1889MCL0020inhibit,Melanocortin Receptor,COS-1,Inhibitor,MCL0020,MC Receptor,anorexia,dose-dependently,s
Potent and selective melanocortin MC4 receptor antagonist (IC50 values are 11.63, 1115 and > 10 000 nM at MC4, MC3 and MC1 receptors respectively). Significantly reverses stress-induced anorexia but has no effect on food intake in free-feeding rats. Exhibits anxiolytic-like activity in vivo.
价 格：￥电议型 号：TP1889产 地：中国大陆
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T9098DMG-PEG 2000Inhibitor,therapy,T2D,lPEI/DNA nanoparticle,type II diabete,A549,HepG2,inhibit,HeLa,DMG-
DMG-PEG2000 is a lipid excipient that has been used in combination with other lipids in the formation of lipid nanoparticles. Formulations containing DMG-PEG2000 have been used in the development of lipid nanoparticles for the delivery of mRNA-based vaccines.
价 格：￥电议型 号：T9098产 地：中国大陆
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T8320J14cancer,inhibit,damage,Sulfiredoxin,J14,cytotoxicity,Reactive Oxygen Species,J 14,death,adenocarci
J-14 is an inhibitor of reversible sulfiredoxin(IC50 : 8.1 μM). J14 induces oxidative stress (intracellular ROS accumulation) by inhibiting sulfiredoxin, leading to cytotoxicity and cancer cell death
价 格：￥电议型 号：T8320产 地：中国大陆
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TP1358LPeptide M acetate
Peptide M acetate is a synthetic amino acid (18 amino acids in length which correspond to the amino acid positions 303-322 of bovine S-antigen: DTNLASSTIIKEGIDKTV). Peptide M acetate is capable of inducing experimental autoimmune uveitis in monkeys and Hartley guinea pigs as well as Lewis rats.
价 格：￥电议型 号：TP1358L产 地：中国大陆
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TMA0958Forsythoside Finhibit,Xanthine Oxidase,Forsythoside F,antihyperuricemic,Inhibitor
Arenarioside is a natural product, and GI50 values of 10-16 microM against B16F10 cell.
价 格：￥电议型 号：TMA0958产 地：中国大陆
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T6S0105PeiminineInhibitor,inhibit,Peiminine,Autophagy
1. Peiminine is an effective inhibitor for lung inflammation and pulmonary fibrosis in a rat model of bleomycin-induced lung injury.
价 格：￥电议型 号：T6S0105产 地：中国大陆
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T6917OleuropeinPPARγ,olive,PPAR,Peroxisome proliferator-activated receptors,inhibit,Apoptosis,leaves,Oleu
Oleuropein is an antioxidant polyphenol isolated from olive leaf.
价 格：￥电议型 号：T6917产 地：中国大陆
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T9834(3Z)-1-methyl-3-[2-(4-methylphenyl)-2-oxo-ethylidene]piperazin-2-one(3Z) 1 methyl 3 [2 (4 methylphen
(3Z)-1-methyl-3-[2-(4-methylphenyl)-2-oxo-ethylidene]piperazin-2-one is a chemical agent.
价 格：￥电议型 号：T9834产 地：中国大陆
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T6S1579MonotropeinMonotropein,Inhibitor,inhibit
1. Monotropein has antinociceptive action. 2. Monotropein has anti-apoptosis and anti-catabolic activity in chondrocytes. 3. Monotropein has anti-inflammatory action by inhibition of the expressions of inflammatory mediators via NF-κB inactivation, and support its possible therapeutic role in colitis. 4. Monotrope ininhibit the expressions of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), tumor necrosis factor-α (TNF-α), and interleukin-1β (IL-1β) mRNA in LPS-induced RAW 264.7
价 格：￥电议型 号：T6S1579产 地：中国大陆
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T9808Tetradecylthioacetic acidPeroxisome proliferator-activated receptors,β-Oxidation,inhibit,fatty acid
Tetradecylthioacetic acid is a synthetic fatty acid with a sulfur substitution in the β-position. This modification renders TTA unable to undergo complete β-oxidation and increases its biological activity, including activation of peroxisome proliferator activated receptors (PPARs) with preference for PPARα.
价 格：￥电议型 号：T9808产 地：中国大陆
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T40023Pomalidomide-PEG3-CO2H
Thalidomide-NH-PEG3-propionic acid is a synthesized E3 ligase ligand-linker conjugate. Thalidomide-NH-PEG3-propionic acid incorporates the Thalidomide based cereblon ligand and 3-unit PEG linker used in PROTAC technology.
价 格：￥电议型 号：T40023产 地：中国大陆
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T8012Scyllo-InositolScyllo Inositol,Inhibitor,Abeta,ScylloInositol,Scyllo-Inositol,Amyloid-β,β-amyloid pe
Scyllo-Inositol is one of the inositol stereoisomers, rare in the nature, and expected as a promising disease-modifying therapeutic agent for Alzheimer´s disease.
价 格：￥电议型 号：T8012产 地：中国大陆
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T9986(E/Z)-ZINC09659342(E/Z)-ZINC09659342,Inhibitor,Lbc-RhoA interaction,Ras,(E/Z)ZINC09659342,Ras superf
(E/Z)-ZINC09659342 is an inhibitor of Lbc-Rho A interaction.
价 格：￥电议型 号：T9986产 地：中国大陆
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T7758Thalidomide-O-amido-PEG3-C2-NH2 TFAE3 Ligase Ligand-Linker Conjugates,Cereblon Ligand-Linker Conjuga
Thalidomide-O-amido-PEG3-C2-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate. Thalidomide-O-amido-PEG3-C2-NH2 TFA incorporates the Thalidomide based cereblon ligand and 3-unit PEG linker used in PROTAC technology.
价 格：￥电议型 号：T7758产 地：中国大陆
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T8963CYM2503Neuropeptide Y Receptor,electrographic seizure,NPY receptor,CYM 2503,seizure,inhibit,CYM2503,
CYM2503 is a positive allosteric modulator (PAM) of the GAL2 receptor that potentiates galanin-induced IP1 production in vitro. It has no affinity for the orthosteric galanin binding site of the receptor (as measured by its inability to displace iodinated galanin, or to induce IP1 accumulation on its own).
价 格：￥电议型 号：T8963产 地：中国大陆
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T9333Perfluorooctanoic acidPerfluorooctanoic acid
Perfluorooctanoic acid (PFOA) is a persistent and widespread industry-made chemical.
价 格：￥电议型 号：T9333产 地：中国大陆
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TP1472Tyroserleutidetripeptide,Tyroserleutide,tumor,inhibit,Inhibitor,YSL,Antitumor
Tyroserleutide (YSL), isolated from the degradation products of porcine spleen, is a small molecular tripeptide which inhibits tumor growth both in vitro and in vivo.Tyroserleutide inhibits the growth and metastasis of human hepatocellular carcinoma (HCC).
价 格：￥电议型 号：TP1472产 地：中国大陆
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TP1059Peptide YY (PYY) (3-36), humanNeuropeptide Y Receptor,Inhibitor,NPY receptor,Peptide YY (PYY) (336),
Peptide YY (PYY) (3-36), human is a gut hormone peptide. Peptide YY (PYY) (3-36), human acts as a Y2 receptor agonist to reduce appetite.
价 格：￥电议型 号：TP1059产 地：中国大陆
