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T3S1692Octahydrocurcumin
Octahydrocurcumin has antioxidant and and anti-inflammatory activities, it can inhibit the lipopolysaccharide (LPS)-induced inflammatory response via the mechanism of inhibiting NF-kB translocation to the nucleus. Octahydrocurcumin exhibits potent cytotox
价 格：￥电议型 号：T3S1692产 地：中国大陆
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T3S1641Esculentoside H
Phytolaccaceae has anti-tumor activity, the mechanism may be related to the capacity of Esculentoside H for TNF release.
价 格：￥电议型 号：T3S1641产 地：中国大陆
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T3S1628Vitexin-4''-O-glucoside牡荆素-4''-O-葡萄糖苷；Vitexin -4''-O-glucoside
Vitexin-4´´-O-glucoside could effectively protect ECV-304 cells against cytotoxicity induced by TBHP through resuming mitochondrial function.
价 格：￥电议型 号：T3S1628产 地：中国大陆
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T3S1612kuwanon GKuwanone G；Moracenin B；桑黄酮G；桑黄酮 G
1. Kuwanon G as dual inhibitors of PTP1B and α-glucosidase enzymes, as well as insulin sensitizers, it may potentially be utilized as an effective treatment for Type II diabetes mellitus. 2. Kuwanon G has anti-inflammatory activity, it can attenuate ather
价 格：￥电议型 号：T3S1612产 地：中国大陆
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T3S1416DecursinDecursinol angelate；(+)-Decursin；前胡素；紫花前胡素
1. Decursin is able to attenuate kainic acid-induced seizures and could have potential as an antiepileptic drug. 2. Decursin exhibits hepatoprotective effects , potentially by inhibiting the TGF-β1 induced NOX activation and Smad signaling. 3. Decursin ha
价 格：￥电议型 号：T3S1416产 地：中国大陆
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T3989SMI-16aPIM1/2 Kinase Inhibitor VI
PIM1/2 Kinase Inhibitor VI, a cell-permeable thiazolidinedione compound, acts as an effective, ATP-competitive inhibitor against Pim-1/2 kinases (IC50: 150/20 nM) while exhibiting little or no activity against a panel of 57 other kinases (≤18% inhibition
价 格：￥电议型 号：T3989产 地：中国大陆
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T39516Bocidelpar
Bocidelpar is a modulator of PPARδ with an EC50 of 7.80 nM and improves mitochondrial biogenesis and function in Duchenne Muscular Dystrophy muscle cells.
价 格：￥电议型 号：T39516产 地：中国大陆
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T3938H-HomoArg-OH.HClL-高精氨酸盐酸盐；L-Homoarginine hydrochloride；NSC 145416；L(+)-Homoarginine hydrochloride
L-Homoarginine is a specific inhibitor of liver-type alkaline phosphatase.
价 格：￥电议型 号：T3938产 地：中国大陆
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T3929Kaurenoic acid异贝壳杉烯酸；kaur-16-en-18-oic acid；Kauren-19-Oic Acid；kaurenoate
Kaurenoic acid has anti-inflammatory potential in acetic acid-induced colitis, decreases in MDA level. Kaurenoic acid exerts a uterine relaxant effect acting principally through calcium blockade and in part, by the opening of ATP-sensitive potassium chann
价 格：￥电议型 号：T3929产 地：中国大陆
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T39275BefotertinibD-0316；Befotertinib
Befotertinib (D-0316) is the third-generation EGFR tyrosine kinase inhibitor. Befotertinib can be used for the research of EGFR T790M-positive non-small cell lung cancer (NSCLC).
价 格：￥电议型 号：T39275产 地：中国大陆
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T39161Ro60-0175Ro60-0175
Ro60-0175 is a potent and selective agonist of 5-HT 2C receptor. Ro60-0175 reduces cocaine self-administration, and the ability of cocaine to reinstate responding after extinction of drug-seeking behavior.
价 格：￥电议型 号：T39161产 地：中国大陆
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T3916Ginsenoside F2人参皂苷F2
Ginsenoside F2 has antiproliferative activity against breast cancer stem cells (CSCs). It induces apoptosis in breast CSCs by activating the intrinsic apoptotic pathway and mitochondrial dysfunction.
价 格：￥电议型 号：T3916产 地：中国大陆
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T38843EnavogliflozinDWP-16001
Enavogliflozin is an orally available small molecule and sodium glucose transporter 2 inhibitor.
价 格：￥电议型 号：T38843产 地：中国大陆
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T37314JKE-1674
JKE-1674 is an inhibitor of glutathione peroxidase 4 (GPX4). JKE-1674 is an active metabolite of the GPX4 inhibitor ML-210.
价 格：￥电议型 号：T37314产 地：中国大陆
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T3716RolapitantSCH619734；罗拉吡坦；罗拉匹坦
Rolapitant Hydrochloride is the hydrochloride salt form of rolapitant, an orally bioavailable, centrally-acting, selective, neurokinin 1 receptor (NK1-receptor) antagonist with potential antiemetic activity. Upon oral administration, rolapitant competitiv
价 格：￥电议型 号：T3716产 地：中国大陆
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T3714SUN11602SUN 11602
SUN11602, an aniline compound, mimics the neuroprotective mechanisms of basic fibroblast growth factor. It mimics the neuroprotective effects of bFGF and prevents glutamate-induced neuronal death. It also increases levels of CALB1 gene expression in cereb
价 格：￥电议型 号：T3714产 地：中国大陆
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T3710XMD16-5
XMD16-5 is a TNK2 inhibitor. TNK2 genomic amplification has been associated with late-stage or metastatic lung and prostate Ys. Overexpression of TNK2 promoted metastasis in a mouse model of breast Y. TNK2 signaling is disrupted in breast, prostate and ga
价 格：￥电议型 号：T3710产 地：中国大陆
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T3691(Rac)-SAR131675SAR131675
SAR131675 is an effective and specific VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine kinase activity (IC50: 20 nmol/L) and VEGFR-3 autophosphorylation (IC50: 45 nmol/L) in HEK cells, respectively. SAR131675 is highly specific for VEGFR-3 versus 107 rec
价 格：￥电议型 号：T3691产 地：中国大陆
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T36879LH-Leu-Leu-OMe . HBrH-Leu-Leu-OMe . HBr (16689-14-8 Free base)
H-Leu-Leu-OMe . HBr is a dipeptide condensation product of L-leucine methyl ester generated by human monocytes or polymorphonuclear leukocytes. H-Leu-Leu-OMe . HBr induces endolysosomal pathway stress and selectively eliminates lymphocytes with cytotoxic
价 格：￥电议型 号：T36879L产 地：中国大陆
