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T6210Pifithrin-μPFTμ；2-Phenylethynesulfonamide；NSC 303580
Pifithrin-μ is an inhibitor of p53 and HSP70, with neuroprotective and antitumor activity.
价 格：￥电议型 号：T6210产 地：中国大陆
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T6175ADL-5859ADL5859 HCl；ADL5859 Hydrochloride
ADL5859 HCl is a selective δ-opioid receptor agonist ( Ki: 0.8 nM), selectivity against opioid receptor κ, μ, and little inhibition for the hERG channel.
价 格：￥电议型 号：T6175产 地：中国大陆
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T6159LY-2584702 free base
LY2584702 is a selective, ATP-competitive p70S6K inhibitor(IC50: 4 nM).
价 格：￥电议型 号：T6159产 地：中国大陆
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T6158LDN-193189 HClLDN193189 Hydrochloride
LDN193189 hydrochloride is a selective BMP type I receptor kinases inhibitor.
价 格：￥电议型 号：T6158产 地：中国大陆
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T6103VS-5584VS5584；VS 5584；SB2343
VS-5584 is a pan-PI3K/mTOR kinase inhibitor.
价 格：￥电议型 号：T6103产 地：中国大陆
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T6097GNF-5837GNF5837；GNF 5837
GNF-5837 is a specific, and orally bioavailable pan-TRK inhibitor for TrkA/TrkB (IC50: 8/12 nM).
价 格：￥电议型 号：T6097产 地：中国大陆
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T6058LY2886721
LY2886721, a BACE inhibitor, is used for the therapy of Alzheimer´s Disease.
价 格：￥电议型 号：T6058产 地：中国大陆
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T5S2358Dehydrocorydaline脱氢紫堇碱；Dehydrocorydalin；13-Methylpalmatine
1. Dehydrocorydaline exerts anti-metastatic potential via suppression of MMPs and Bcl-2 signaling in NSCLC cells. 2. Dehydrocorydaline stimulates p38 MAPK activation, which can enhance heterodimerization of MyoD and E proteins, thus resulting in MyoD acti
价 格：￥电议型 号：T5S2358产 地：中国大陆
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T5S1058Triptonide雷公藤内酯酮；PG 492；NSC 165677
1. Triptonide is effective in the treatment of autoimmune diseases and has potent antileukemic and antitumor activities. 2. Triptonide possesses anti-inflammatory activity, upregulate the expression of IL-37, and this expression was suppressed by ERK1/2 a
价 格：￥电议型 号：T5S1058产 地：中国大陆
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T5S0658Corynoxine柯诺辛；柯诺辛碱
Corynoxine is a natural oxindole alkaloid and induces autophagy in different neuronal cell lines, including N2a and SHSY-5Y cells.
价 格：￥电议型 号：T5S0658产 地：中国大陆
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T5S0581Sec-O-Glucosylhamaudol亥茅酚苷；Hamaudol 3-glucoside
Sec-O-glucosylhamaudol has anti-inflammatory effect through regulation of p38 Mitogen-Activated Protein Kinase in Lipopolysaccharide-stimulated RAW264.7 cell line. Intrathecal sec-O-glucosylhamaudol has a very strong antinociceptive effect in the formalin
价 格：￥电议型 号：T5S0581产 地：中国大陆
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T5997TBAJ-587
TBAJ-587 is a potent anti-tuberculosis agent. TBAJ-587 inhibits M.tb strain H37Rv growth with MIC90s of 0.006 and <0.02 μg/mL in MABA and LORA assay, respectively. BAJ-587 has more potent activity against M. tuberculosis and better efficacy in animal mode
价 格：￥电议型 号：T5997产 地：中国大陆
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T5891D-ERYTHRO-SPHINGOSINEtrans-4-Sphingenine；erythro-C18-Sphingosine；Erythrosphingosine；鞘氨醇；D-鞘氨醇
D-erythro-Sphingosine is a protein kinase C (PKC) inhibitor. D-erythro-Sphingosine (Erythrosphingosine) is also a PP2A activator
价 格：￥电议型 号：T5891产 地：中国大陆
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T58902,4-Dihydroxybenzoic acid
2,4-Dihydroxybenzoic acid is found in alcoholic beverages.2, 4-Dihydroxybenzoic acid is a food flavour ingredient and flavour modifie.
价 格：￥电议型 号：T5890产 地：中国大陆
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T5889Kojic acid
Kojic acid is a fungal metabolite that inhibits tyrosinase, an enzyme involved in melanin synthesis, with an IC50 value of 30.6 μM for mushroom tyrosinase.
价 格：￥电议型 号：T5889产 地：中国大陆
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T58885-Methoxysalicylic acid5-甲氧基水杨酸；5-MeOSA
5-Methoxysalicylic acid is a natural product, used as a useful matrix in the MALDI MS analysis of oligonucleotides when combined with spermine
价 格：￥电议型 号：T5888产 地：中国大陆
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T58877-Hydroxy-3,4-dihydro-2(1H)-quinolinone3,4-二氢-7-羟基-2(1H)-喹啉酮；3,4-Dihydro-7-hydroxy-2(1H)-quinolinone
3,4-Dihydro-7-hydroxy-2(1H)-quinolinone (7- Hydroxy- 3, 4- dihydro- 2(1H) - quinolinone) is a weak MAO-A inhibitor(with an IC50 of 183 μM) .
价 格：￥电议型 号：T5887产 地：中国大陆
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T58864-Phenylbutyric acidBenzenebutyric acid；苯丁酸；4-苯基丁酸
Benzenebutyric acid is an inhibitor of HDAC,and is an antineoplastic agent.
价 格：￥电议型 号：T5886产 地：中国大陆
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T5885N-Acetyl-D-galactosamineGalNAc；2-乙酰胺基-2-脱氧-D-半乳糖
N-Acetyl-d-galactosamine (GalNAc) is a terminal essential amino sugar derived from galactose and forms the antigens of blood group A in humans.
价 格：￥电议型 号：T5885产 地：中国大陆
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T5884Chelidamic acid4-氧代-1,4-二氢-2,6-吡啶二甲酸；白屈氨酸
Chelidamic acid is a heterocyclic organic acid with a pyran skeleton. Chelidamic acid is inhibitors of glutamate decarboxylase, with a Ki of 33 μM.
价 格：￥电议型 号：T5884产 地：中国大陆
