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T33422MK-0873；化合物MK-0873MK 0873|||MK0873；MK 0873|||MK0873
MK-0873 is a novel and potent selective phosphodiesterase 4 (PDE4) inhibitor.
价 格：￥电议型 号：T33422产 地：中国大陆
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T33421MK-0686；化合物MK-0686MK0686；MK0686
MK-0686 is an orally available bradykinin B1 receptor antagonist with potential anti-inflammatory activity.
价 格：￥电议型 号：T33421产 地：中国大陆
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T33420LMK-0668 Mesylate；化合物 T33420LMK-0668|||MK0668|||MK 0668；MK-0668|||MK0668|||MK 0668
MK-0668 Mesylate is the mesylate form of MK-0668 that is a very potent and orally active very late antigen-4 antagonist.
价 格：￥电议型 号：T33420L产 地：中国大陆
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T33420MK-0668；化合物 T33420MK 0668；MK 0668
MK-0668 is a very potent and orally active very late antigen-4 antagonist.
价 格：￥电议型 号：T33420产 地：中国大陆
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T33419MK-0493 HCl；化合物 T33419MK 0493|||MK-0493|||MK0493；MK 0493|||MK-0493|||MK0493
MK-0493 is a novel, potent, and selective agonist for melanocortin receptor 4 (MC4R).
价 格：￥电议型 号：T33419产 地：中国大陆
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T33418MK-0359；化合物 T33418L-454560|||L454560|||MK 0359|||L 454560；L-454560|||L454560|||MK 0359|||L 454560
MK-0359 (L454560) is a selective and effective oral PDE4 inhibitor for the treatment of chronic asthma.
价 格：￥电议型 号：T33418产 地：中国大陆
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T33417MK 410；化合物 T33417MK-410|||MK410；MK-410|||MK410
MK 410 is an indomethacin analogue and anti-inflammatory agent that induces changes in the immune system by inhibiting plasma neutral protease activity.
价 格：￥电议型 号：T33417产 地：中国大陆
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T33416MK 0927；化合物 T33416MK-0927|||MK0927；MK-0927|||MK0927
MK 0927 is a potential bioactive agent. No detail information yet.
价 格：￥电议型 号：T33416产 地：中国大陆
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T33415MK 0767；化合物 T33415MK0767|||MK-0767；MK0767|||MK-0767
MK 0767 is a dual peroxisome proliferator-activated receptor (PPAR) α/γ agonist that has been investigated as a potential treatment for type 2 diabetes and dyslipidemia.
价 格：￥电议型 号：T33415产 地：中国大陆
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T33414MK 0434；化合物 T33414MK0434|||MK434|||MK 434|||MK-0434|||MK-434；MK0434|||MK434|||MK 434|||MK-0434|||MK-
MK 0434 is a steroid 5α-reductase inhibitor and hormone antagonist associated with a significant reduction in DHT.
价 格：￥电议型 号：T33414产 地：中国大陆
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T3320Dizocilpine Maleate；地卓亚平马来酸盐(+)-Mk-801 Hydrogen Maleate|||MK 801|||Dizocilpine hydrogen maleate|||(+
Dizocilpine Maleate (MK 801) is a potent noncompetitive antagonist of the NMDA receptor (RECEPTORS, N-METHYL-D-ASPARTATE) with Kd of 37.2 nM in rat brain membranes. The drug has been considered for the wide variety of neurodegenerative conditions or disorders in which NMDA receptors may play an important role.
价 格：￥电议型 号：T3320产 地：中国大陆
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T32840Locustakinin；化合物 T32840Ala-phe-ser-ser-trp-gly-NH2|||Lomk peptide|||Locustakinn；Ala-phe-ser-ser-trp-
Locustakinin is a myotropic peptide.
价 格：￥电议型 号：T32840产 地：中国大陆
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T3231Niraparib；尼拉帕尼MK-4827；尼拉帕尼|||MK-4827
Niraparib (MK-4827) is a PARP inhibitor that selectively inhibits PARP1 and PARP2 (IC50=3.8/2.1 nM). Niraparib has antitumor activity, inhibits DNA damage repair, and induces apoptosis.
价 格：￥电议型 号：T3231产 地：中国大陆
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T31813Fludalanine；化合物 T31813MK641|||D-Alanine-2-d, 3-fluoro-|||3-Fluoro-D-(2-2H)alanine；MK641|||D-Alanine-
Fludalanine (MK641), an analogue of D-alanine, irreversiably inactivates racemase and also inhibits synthase. When used in combination with cycloserine, it has been found to be more active against a variety of non-mycobacterium organisms than fludalanine or cycloserine alone.
价 格：￥电议型 号：T31813产 地：中国大陆
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T3148MK-571 sodium；化合物Propanoic acidL-660711 (sodium salt)|||L-660711 sodium salt|||Verlukast sodium|||L-
MK-571 sodium (L-660711 sodium salt) is a selective, orally active antagonist of the CysLT1 receptor. MK-571 sodium is a multidrug resistance protein-2 (ABCC2, Mrp2) inhibitor used to demonstrate the role of Mrp2 in the cellular efflux of drugs, xenobiotics, and their conjugates. MK-571 sodium can inhibit the synthesis of K-4′-O-GlcA (19.7 μM). MK571 dose-dependently inhibits the intracellular biosynthesis of all flavonol sulphates and glucuronides by Caco-2 cells. MK-571 sodium significantly in
价 格：￥电议型 号：T3148产 地：中国大陆
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T31042CP-195543；化合物 T31042UNII-YB1F0V77MK|||CP 195543；UNII-YB1F0V77MK|||CP 195543
CP-195543 is an effective leukotriene B4 antagonist for the treatment of inflammatory diseases.
价 格：￥电议型 号：T31042产 地：中国大陆
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T30527BMS-488043；化合物BMS-488043CHEMBL238103|||UNII-MKS21EJ435|||BMS 043|||BMS488043|||BMS 488043；CHEMBL2381
BMS-488043 is a novel and unique oral small molecule HIV fusion inhibitor that inhibits the attachment of Human Immunodeficiency Virus type 1 (HIV-1) to CD4(+) lymphocytes.BMS-488043 is used for the treatment of immune disorders, infections, and genitourinary disorders, and can be used in the study of HIV infect
价 格：￥电议型 号：T30527产 地：中国大陆
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T29254MK-0963；化合物 T29254MK-0963
(5Alpha)-23-methyl-4-aza-21-norchol-1-ene-3,20-dione is a bioactive chemical.
价 格：￥电议型 号：T29254产 地：中国大陆
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T29069Uprifosbuvir；化合物 T29069MK3682|||IDX21437|||IDX 21437|||MK 3682|||IDX-21437|||MK-3682；MK3682|||IDX214
Uprifosbuvir is an inhibitor of uridine nucleotide analog HCV NS5B polymerase.
价 格：￥电议型 号：T29069产 地：中国大陆
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T29059UMK57；化合物UMK57UMK 57|||UMK-57；UMK 57|||UMK-57
UMK57 is a CENP-Ei and MCAK enhancer, selectively promoting k-MT attachment error correction to inhibit chromosome missegregation of small molecule compounds, and can improve chromosome separation conservation by disrupting the stability of kinetosomal microtubule (k-MT) attachment during mitosis.
价 格：￥电议型 号：T29059产 地：中国大陆
