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T11599Ibiglustat (L-Malic acid)；化合物Ibiglustat (L马来酸)Ibiglustat L-Malic acid|||GZ402671 (L-Malic acid)|||Ve
Ibiglustat (L-Malic acid) (Ibiglustat L-Malic acid) is a selective, brain-penetrant, and allosteric inhibitor of glucosylceramide synthase. Ibiglustat (L-Malic acid) can be used in studies about PD Parkinson’s disease, SRT in Fabry’s and Gaucher’s.
价 格：￥电议型 号：T11599产 地：中国大陆
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T11598IAXO-102；化合物IAXO-102IAXO-102
IAXO-102 is a TLR4 antagonist that negatively regulates TLR4 signaling. It inhibits MAPK and p65 NF-κB phosphorylation and expression of TLR4 dependent proinflammatory protein. IAXO-102 also prevents experimental abdominal aortic aneurysm development.
价 格：￥电议型 号：T11598产 地：中国大陆
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T11597LIACS-9571 Hydrochloride (1800477-30-8 free base)；化合物 T11597LIACS-9571 Hydrochloride|||ASIS-P040 Hydr
IACS-9571 Hydrochloride is a selective and potent inhibitor of TRIM24 and BRPF1, (IC50: 8 nM for TRIM24; Kds: 31 nM and 14 nM for TRIM24 and BRPF1).
价 格：￥电议型 号：T11597L产 地：中国大陆
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T11597IACS-9571；化合物 T11597ASIS-P040；ASIS-P040
IACS-9571 is a selective and potent inhibitor of TRIM24 and BRPF1, (IC50: 8 nM for TRIM24; Kds: 31 nM and 14 nM for TRIM24 and BRPF1).
价 格：￥电议型 号：T11597产 地：中国大陆
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T11596IACS-8803；化合物 T11596IACS-8803
IACS-8803 is a potent cyclic dinucleotide STING agonist that exhibits strong systemic antitumor efficacy.
价 格：￥电议型 号：T11596产 地：中国大陆
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T11595IACS-8779；化合物 T11595IACS-8779
IACS-8779 is a potent STING agonist that efficiently stimulates interferon gene activity and exhibits strong systemic antitumor effects.
价 格：￥电议型 号：T11595产 地：中国大陆
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T11594I2906；化合物 T11594I2906
I2906 showed antimycobacterial and cytotoxic activity against mycobacterium tuberculosis.
价 格：￥电议型 号：T11594产 地：中国大陆
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T11593I-OMe-Tyrphostin AG 538；化合物T11593I-OMe-AG 538；I-OMe-AG 538
I-OMe-Tyrphostin AG 538 is a specific IGF-1R inhibitor and ATP-competitive inhibitor of PI5P4Kα (IC50: 1 ?M).I-OMe-Tyrphostin AG 538 inhibits IGF-1R-mediated signaling and exhibits preferential cytotoxicity to nutrient-deficient PANC1 cells.
价 格：￥电议型 号：T11593产 地：中国大陆
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T11592Hydroxyzine D8；化合物 T11592Hydroxyzine D8
Hydroxyzine D8, a deuterium-labeled version of Hydroxyzine, acts as a histamine H1-receptor antagonist.
价 格：￥电议型 号：T11592产 地：中国大陆
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T11591Hydroxyzine D4羟嗪 D4羟嗪 D4
Hydroxyzine D4 is a deuterium-labeled variation of Hydroxyzine, a chemical compound known for its anticholinergic, anxiolytic, and analgesic properties. It is classified as a heterocyclic histamine H1-receptor antagonist.
价 格：￥电议型 号：T11591产 地：中国大陆
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T11590(-)-Hydroxycitric acid；(-)-羟基柠檬酸Garcinia acid；Garcinia acid|||(-)-羟基柠檬酸
(-)-Hydroxycitric acid (Garcinia acid) (Garcinia acid) is the principal acid of fruit rinds of Garcinia cambogia. It is a potent and competitive inhibitor of ATP citrate lyase. (-)-Hydroxycitric acid suppresses fatty acid synthesis, food intake, lipogenesis, and induced weight loss.
价 格：￥电议型 号：T11590产 地：中国大陆
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T1159Leflunomide来氟米特SU101|||RS-34821|||HWA486|||来氟米特
Leflunomide (HWA486) is an immunomodulatory agent used in the therapy of rheumatoid arthritis and psoriatic arthritis.
价 格：￥电议型 号：T1159产 地：中国大陆
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T11577BAY 59-9435；化合物 T11577HSL-IN-2；HSL-IN-2
HSL-IN-2 is a selective inhibitor of Hormone Sensitive Lipase (HSL; IC50: 0.023 μM).
价 格：￥电议型 号：T11577产 地：中国大陆
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T1156Palonosetron hydrochloride；盐酸帕洛诺司琼RS 25259 197|||Palonosetron HCl|||RS 25259；盐酸帕洛诺司琼|||RS 25259 197|
Palonosetron hydrochloride (RS 25259) is a 5-HT3 antagonist used in the prevention and treatment of chemotherapy-induced nausea and vomiting.
价 格：￥电议型 号：T1156产 地：中国大陆
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T11559HG-12-6；化合物 T11559HG-12-6
HG-12-6 is a type II inhibitor of IRAK4. HG-12-6 shows preferential binding to unphosphorylated inactive IRAK4 (IC50: 165 nM). HG-12-6 can modulate IRAK4 activity in autoimmunity and inflammation.
价 格：￥电议型 号：T11559产 地：中国大陆
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T11496GSK598809；化合物 T11496GSK598809
GSK598809 is a selective and potent dopamine D3 Receptor (DRD3) antagonist (pKi: 8.9).
价 格：￥电议型 号：T11496产 地：中国大陆
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T11492GSK2983559 free acid；化合物GSK2983559 free acidGSK2983559 free acid
GSK2983559 free acid is an effective and selective inhibitor of receptor-interacting protein 2 (RIP2). GSK2983559 free acid shows excellent activity in blocking many proinflammatory cytokine responses in human inflammatory bowel disease explant samples an
价 格：￥电议型 号：T11492产 地：中国大陆
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T11477GSK1059865；化合物 T11477GSK1059865
GSK1059865 is a potent antagonist of the orexin 1 receptor.
价 格：￥电议型 号：T11477产 地：中国大陆
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T11459GPR40 agonist 1；化合物 T11459GPR40 agonist 1
GPR40 agonist 1 is an effective new GPR40 agonist (EC50s: 17 nM and 2 nM for rGPR40 and hGPR40).
价 格：￥电议型 号：T11459产 地：中国大陆
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T11359gamma-secretase modulator 2；化合物 T11359gamma-secretase modulator 2
Gamma-secretase modulator 2 is a potent, selective compound for the treatment of Alzheimer´s disease, specifically designed to modulate γ-secretase activity. This modulation selectively attenuates the production of Aβ(1-42), addressing diseases associated with Aβ deposition in the brain, particularly Alzheimer´s disease.
价 格：￥电议型 号：T11359产 地：中国大陆
