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T2791Pectolinarin柳穿鱼叶苷柳穿鱼叶苷|||大蓟苷
Pectolinarin is a Cirsium isolate with anti-inflammatory activity.
价 格：￥电议型 号：T2791产 地：中国大陆
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T27899LY 215891；化合物 T27899LY215891|||LY-215891；LY215891|||LY-215891
LY 215891 is a compound that exhibits potent Gram-negative and Gram-positive antibacterial activity.
价 格：￥电议型 号：T27899产 地：中国大陆
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T27891LY195448 HCl；化合物 LY195448 HClLY195448|||UNII-BR0DFE3GF6|||LY-195448；LY195448|||UNII-BR0DFE3GF6|||LY-
LY195448 HCl is a phenethanolamine shown anti-tumour activity. It blocks cells at metaphase.
价 格：￥电议型 号：T27891产 地：中国大陆
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T27889LY191704；化合物 T27889LY 191704|||LY-191704；LY 191704|||LY-191704
LY 191704 is a 5α-reductase type 1 inhibitor.
价 格：￥电议型 号：T27889产 地：中国大陆
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T27799LAS191859；化合物 T27799LAS-191859|||LAS 191859；LAS-191859|||LAS 191859
LAS191859 is a CRTH2/DP2 antagonist with IC50 values of 7.6, 9.58, 14 and 15.5nM for recombinant guinea pig, human, rat and mouse CRTH2/DP2 receptors, respectively. LAS191859 has a residence time half-life of 21h at CRTh2 that translates into a long-lasting in vivo efficacy that is independent of plasma levels
价 格：￥电议型 号：T27799产 地：中国大陆
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T27798Lapisteride；拉匹雄胺CS891B|||CS-891|||CS-891B|||CS891；CS891B|||CS-891|||CS-891B|||CS891
Lapisteride (CS-891) a steroidal 5α-reductase inhibitor is used to treat benign prostatic hyperplasia (BPH) and androgenetic alopecia and may be effective in preventing or treating AGA .
价 格：￥电议型 号：T27798产 地：中国大陆
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T27791Ladarixin Sodium；化合物 T27791DF 2156A|||DF-2156|||DF2156A|||DF2156|||DF 2156|||DF-2156A；DF 2156A|||DF-
Ladarixin Sodium, an Chemokine CXCR antagonist, is used potentially for the treatment of type I diabetes.
价 格：￥电议型 号：T27791产 地：中国大陆
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T27787LL-797,591 hydrochloride；L-797,591盐酸盐L-797,591 hydrochloride(217480-24-5 Free base)；L-797,591 hydroch
L-797,591 hydrochloride is active for somatostatin receptor isoform 1 (SSTR1). L-797,591 hydrochloride is commonly used in combination with AG1478 to enhance p-ERK5 expression in SSTR1 cells. L-797,591 hydrochloride significantly enhanced p38 phosphorylation in cotransfected cells, and this effect was reversed in combination with AG1478.
价 格：￥电议型 号：T27787L产 地：中国大陆
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T27787L-797,591；化合物 T27787L-797,591
L-797,591 is a selective agonist of somatostatin receptor subtype 1.
价 格：￥电议型 号：T27787产 地：中国大陆
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T27718KCO-912；化合物 T27718KCO-912
KCO-912 is a potent and selective opener of ATP-dependent potassium (K ATP) channels. KCO-912 suppresses airways hyperreactivity at doses devoid of cardiovascular effects.
价 格：￥电议型 号：T27718产 地：中国大陆
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T27691JNJ-DGAT2-A；化合物JNJ-DGAT2-AJNJDGAT2A；JNJDGAT2A
JNJ-DGAT2-A, a specific inhibitor of DGAT2(IC50 = 0.14 μM), can be used in studies about the synthesis of triglycerides.
价 格：￥电议型 号：T27691产 地：中国大陆
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T27684JNJ-42259152；化合物 T27684JNJ42259152|||JNJ 42259152；JNJ42259152|||JNJ 42259152
JNJ-42259152 is a phosphodiesterase 10A PET tracer.
价 格：￥电议型 号：T27684产 地：中国大陆
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T27674JNJ-27141491；化合物 T27674JNJ 27141491；JNJ 27141491
JNJ-27141491 is a potent, noncompetitive antagonist of human CCR2.
价 格：￥电议型 号：T27674产 地：中国大陆
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T27672JNJ-26489112；化合物 T27672JNJ-26489112
JNJ-26489112 is a drug potentially for the treatment of depression and photosensitive epilepsy.
价 格：￥电议型 号：T27672产 地：中国大陆
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T27668JNJ-2408068；化合物 T27668R170591|||R 170591|||HE066500|||R-170591|||HE-066500|||HE 066500；R170591|||R 1
JNJ-2408068 is an inhibitor of respiratory syncytial virus (RSV). JNJ-2408068 exhibited potent antiviral activity with EC50 of 2.1 nM. A similar inhibitory effect was observed in a RSV-mediated cell fusion assay (EC50= 0.9 nM). JNJ-2408068 interferes with RSV fusion through a mechanism involving a similar interaction with the F protein.
价 格：￥电议型 号：T27668产 地：中国大陆
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T27658JNJ-10191584；化合物 T27658VUF-6002|||JNJ10191584；VUF-6002|||JNJ10191584
JNJ-10191584, a potent and selective antagonist at the histamine H4 receptor, has antiinflammatory and analgesic effects in animal studies of acute inflammation.
价 格：￥电议型 号：T27658产 地：中国大陆
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T27625IQP-0528；化合物IQP-0528SJ-3991|||SJ3991|||IQP0528；SJ-3991|||SJ3991|||IQP0528
IQP-0528 is a potent non-nucleoside reverse transcriptase inhibitor (NNRTI) that has potential for the treatment of HIV infection by blocking viral entry and shows antiviral activity as a microbicidal gel. . IQP-0528 showed inhibition of both HIV-1 and HIV-2, with an EC50 of 0.2 nM for HIV-1 and 100 nM for HIV-2.
价 格：￥电议型 号：T27625产 地：中国大陆
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T27596Imazodan hydrochloride；伊马唑旦盐酸盐CI914 HCl|||CI-914 HCl|||CI 914 HCl|||Imazodan HCl；CI914 HCl|||CI-914
Imazodan hydrochloride (CI-914 HCl) is a potent and selective type III phosphodiesterase inhibitor used in the treatment of chronic congestive heart failure.
价 格：￥电议型 号：T27596产 地：中国大陆
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T27591II-B08；化合物 T27591II-B 08|||FAP1 Inhibitor|||II-B-08|||LMWPTP Inhibitor|||Lyp Inhibitor III|||CD45 In
II-B08 is a cell-permeable SHP2 inhibitor (IC50 = 5.5 ?M). II-B08 blocks growth factor stimulated ERK1/2 activation and hematopoietic progenitor proliferation.
价 格：￥电议型 号：T27591产 地：中国大陆
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T27588Ifetroban；伊非曲班BMS180291|||BMS-180291|||BMS 180291-02；伊非曲班|||BMS180291|||BMS-180291|||BMS 180291-02
Ifetroban is a potent and selective TxA2/PGH2 receptor antagonist.
价 格：￥电议型 号：T27588产 地：中国大陆
