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产品数：86101
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T28056MK319；化合物 T28056MK 319|||MK-319；MK 319|||MK-319
MK319 is an AKR1B10 inhibitor.
价 格：￥电议型 号：T28056产 地：中国大陆
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T28055MK204；化合物 T28055MK-204|||MK 204；MK-204|||MK 204
MK204 is an inhibitor of AKR1B10, a tumor marker and promising antineoplastic target.
价 格：￥电议型 号：T28055产 地：中国大陆
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T28054MK181；化合物 T28054MK 181|||MK-181；MK 181|||MK-181
MK181 is an inhibitor of AKR1B10, a tumor marker and promising antineoplastic target.
价 格：￥电议型 号：T28054产 地：中国大陆
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T28053MK-0736；化合物 T28053MK0736；MK0736
MK-0736 is a potent and selective 11β-HSD-1 inhibitor.
价 格：￥电议型 号：T28053产 地：中国大陆
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T28052MK-0703；化合物 T28052L-791515|||MK0703|||L791515|||MK 0703|||L 791515；L-791515|||MK0703|||L791515|||MK
MK-0703 is a selective cyclooxygenase-2 inhibitor.
价 格：￥电议型 号：T28052产 地：中国大陆
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T28051MK 3118；化合物 T28051MK3118|||SCY078|||SCY-078|||MK-3118|||SCY 078；MK3118|||SCY078|||SCY-078|||MK-3118|
MK 3118, a glucan synthase inhibitor, is used potentially for the treatment of candida infection and aspergillosis.
价 格：￥电议型 号：T28051产 地：中国大陆
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T28050MJN228；化合物 T28050MJN 228|||MJN-228；MJN 228|||MJN-228
MJN228 is a selective ligand for the lipid-binding protein nucleobindin 1 (NUCB1). MJN228 blocks binding of the probe arachidonoyl ethanolamide-diazirine with an IC50 value of 3.3 ?M. MJN228 prevents probe binding to NUCB1 in Neuro2a cells at concentrations as low as 10 ?M.
价 格：￥电议型 号：T28050产 地：中国大陆
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T2805Chlorogenic Acid；绿原酸NSC-407296|||3-O-Caffeoylquinic acid|||Heriguard；NSC-407296|||3-O-Caffeoylquinic
Chlorogenic acid, as a major phenolic compound in honeysuckle, possesses potential antioxidant, antibacterial, anti-inflammatory, and anticancer activities. It can be utilized in research related to the treatment of advanced cancer and impaired glucose tolerance.
价 格：￥电议型 号：T2805产 地：中国大陆
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T27805LDC3140；化合物 T27805LDC 3140|||LDC-3140|||LDC043140；LDC 3140|||LDC-3140|||LDC043140
LDC3140 is a potent inhibitor of Cyclin-dependent kinase 7 (CDK7).
价 格：￥电议型 号：T27805产 地：中国大陆
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T27461GSK2336805；化合物 T27461GSK 2336805|||GSK-2336805|||JNJ-56914845|||GSK-805|||GSK805；GSK 2336805|||GSK-2
GSK-2336805 is a HCV NS5A inhibitor. GSK2336805 retained activity on chimeric replicons containing NS5A patient sequences from genotype 1 and patient and consensus sequences for genotypes 4 and 5 and part of genotype 6.
价 格：￥电议型 号：T27461产 地：中国大陆
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T26805Bicyclomycin；化合物 T26805Bicozamycin；Bicozamycin
Bicyclomycin is a broad spectrum antibiotic active against Gram-negative bacteria and the Gram-positive bacterium, Micrococcus luteusn.
价 格：￥电议型 号：T26805产 地：中国大陆
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T26449A 80556；化合物 T26449A-80556|||A80556；A-80556|||A80556
A 80556, a fluoroquinolone antibiotic, has potent antibacterial activity against gram-positive, gram-negative, and anaerobic organisms.
价 格：￥电议型 号：T26449产 地：中国大陆
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T2623PD98059；化合物PD 98059PD 98059；PD 98059
PD98059 is an MEK inhibitor that inhibits MEK1 and MEK2 (IC50=2/50 μM) and is non-ATP-competitive. PD98059 is also antagonistic as a ligand for AHR. PD98059 inhibits autophagy.
价 格：￥电议型 号：T2623产 地：中国大陆
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T25805Metoquizine；化合物 T25805Ly-42406|||Ly 42406|||Ly42406|||Lilly 42406；Ly-42406|||Ly 42406|||Ly42406|||Li
Metoquizine is an anticholinergic compound. It is a muscarinic acetylcholine receptor antagonist that has been used to treat ulcers.
价 格：￥电议型 号：T25805产 地：中国大陆
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T25252Cimoxatone；化合物 T25252MD-780515|||MD780515|||MD 780515；MD-780515|||MD780515|||MD 780515
Cimoxatone is used as a Monoamine Oxidase Inhibitor.
价 格：￥电议型 号：T25252产 地：中国大陆
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T2501Canertinib dihydrochloride卡奈替尼二盐酸盐CI-1033 dihydrochloride|||PD-183805 dihydrochloride|||Canertinib||
Canertinib dihydrochloride (PD-183805 dihydrochloride) is the hydrochloride salt of an orally bio-available quinazoline with potential antineoplastic and radiosensitizing activities.
价 格：￥电议型 号：T2501产 地：中国大陆
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T2485Baricitinib；巴瑞克替尼INCB028050|||LY3009104；INCB028050|||LY3009104|||巴瑞克替尼
Baricitinib (INCB028050) is an orally bioavailable inhibitor of Janus kinases 1 and 2 (JAK1/2), with potential anti-inflammatory, immunomodulating and antineoplastic activities.
价 格：￥电议型 号：T2485产 地：中国大陆
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T24805SMA-12b；化合物 T24805SMA 12b|||SMA12b；SMA 12b|||SMA12b
SMA-12b is an IL-1 inhibitor.
价 格：￥电议型 号：T24805产 地：中国大陆
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T24365L 858051；化合物 T243657B-Forskolin|||L858051|||Dmpb-forskolin|||L-858051；7B-Forskolin|||L858051|||Dmpb-
L 858051 activates adenylate cyclase. It also inhibits glucose transport in rat adipocytes.
价 格：￥电议型 号：T24365产 地：中国大陆
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T24304L 648051；化合物 T243044-Apsob|||L48051|||L-648051；4-Apsob|||L48051|||L-648051
L 648051 is a leukotriene D4 receptor antagonist.
价 格：￥电议型 号：T24304产 地：中国大陆
