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T2696PRT062607 hydrochloride；化合物PRT062607 hydrochloridePRT062607 (P505-15, BIIB057) HCl|||P505-15 Hydroch
PRT062607 hydrochloride (P505-15 Hydrochloride) is a selective inhibitor of Syk (IC50: 1 nM). It displays at least 80-fold selectivity for Syk over other kinases.
价 格：￥电议型 号：T2696产 地：中国大陆
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T26564ADCI；化合物 T26564SGB-017|||SGB017|||SGB 017；SGB-017|||SGB017|||SGB 017
ADCI is an inhibitor of voltage-activated sodium channels and N-methyl-D-aspartate (NMDA)-receptor-gated channels. Inhibition of sodium channels by ADCI was voltage dependent. High doses of ADCI increased dopamine metabolism in the prefrontal cortex and/or in the nucleus accumbens, but not in the dorsal striatum.
价 格：￥电议型 号：T26564产 地：中国大陆
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T26505AB023b；化合物 T26505AB-023b|||AB 023b；AB-023b|||AB 023b
AB023b is an antibiotic with antifungal properties.
价 格：￥电议型 号：T26505产 地：中国大陆
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T26504AB023a；化合物 T26504AB 023a|||AB-023a；AB 023a|||AB-023a
AB023a is an antibiotic with antifungal properties.
价 格：￥电议型 号：T26504产 地：中国大陆
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T2647IDO5L；化合物INCB024360 analogueINCB024360 analogue|||INCB14943；INCB024360 analogue|||INCB14943
IDO5L (INCB024360 analogue) is an effective IDO1 inhibitor(IC50=10 nM).
价 格：￥电议型 号：T2647产 地：中国大陆
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T25927Pegnivacogin；化合物 T25927RB-006|||RB 006|||RB006；RB-006|||RB 006|||RB006
Pegnivacogin is a coagulation factor IXa RNA aptamer inhibitor.
价 格：￥电议型 号：T25927产 地：中国大陆
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T25394ETB067；化合物 T25394ETB-067|||ETB 067；ETB-067|||ETB 067
ETB067, an H-89 analog, acts as a PKA and AKT1 inhibitor with specificity on no longer inhibiting CAMK2B and neither affecting viability of mice nor causing any detectable tissue damage at the dose given.
价 格：￥电议型 号：T25394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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T24845T16A(inh)-B01；化合物 T24845T16Ainh-B01|||T16A(inh)B01|||T16AinhB01|||T16Ainh B01；T16Ainh-B01|||T16A(inh
T16A(inh)-B01 is the Ca(2+)-activated Cl(-) Channel, Ano1 class B inhibitor.
价 格：￥电议型 号：T24845产 地：中国大陆
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T2476INCB032304；化合物T24764-(1H-Pyrazol-4-yl)-7-((2-(trimethylsilyl)ethoxy)-methyl)-7H-pyrrolo[2,3-d]pyrimi
INCB032304 is an important pharmaceutical intermediate. It can be used in the preparation of Ruxolitinib phosphate (I008849), a janus kinase inhibitor, and in the preparation of Barretinib.
价 格：￥电议型 号：T2476产 地：中国大陆
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T24496MPT0B002；化合物 T24496MPT-0-B-002|||MPT 0 B 002；MPT-0-B-002|||MPT 0 B 002
MPT0B002 is a microtubule inhibitor that acts by downregulating T315I mutant Bcr-Abl and inducing apoptosis of imatinib-resistant chronic myeloid leukemia cells.
价 格：￥电议型 号：T24496产 地：中国大陆
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T23891CJB-090 2HCl；化合物 T23891CJB 090 dihydrochloride|||CJB090 dihydrochloride|||CJB090 2HCl|||CJB-090 dihy
CJB-090 2HCl is a partial agonist of the dopamine D3 receptor.
价 格：￥电议型 号：T23891产 地：中国大陆
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T23770B07 hydrochloride；化合物 T23770B 07 HCl|||B-07 HCl|||B-07 hydrochloride|||B07 HCl|||B 07 hydrochloride；
B07 hydrochloride is a CCR5 antagonist-based inhibitor of HIV-1 entry.
价 格：￥电议型 号：T23770产 地：中国大陆
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T2330Rilpivirine；利匹韦林TMC278|||R278474|||DB08864；TMC278|||R278474|||利匹韦林|||DB08864
Rilpivirine (R278474) is a diarylpyrimidine derivative and reverse transcriptase inhibitor with antiviral activity against HIV-1 that is used in the treatment of HIV infections.
价 格：￥电议型 号：T2330产 地：中国大陆
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T2286BIIB021；化合物BIIB-021BIIB 021|||CNF2024|||BIIB-021；BIIB 021|||CNF2024|||BIIB-021
BIIB021 (CNF2024) is an orally-available, fully synthetic inhibitor of HSP90(Ki=1.7 nM, EC50=38 nM).
价 格：￥电议型 号：T2286产 地：中国大陆
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T2260GW96622-氯-5-硝基-N-苯基苯酰胺2-氯-5-硝基-N-苯基苯酰胺|||TIMTEC-BB SBB006523|||GW 9662
GW9662 (TIMTEC-BB SBB006523) is a specific PPARγ antagonist (IC50: 3.3 nM, in a cell-free assay), with 100 to 1000-fold functional selectivity for PPARγ than PPARα/δ in cells.
价 格：￥电议型 号：T2260产 地：中国大陆
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T22345INCB054329；化合物INCB054329INCB-054329,INCB-54329|||INCB-54329；INCB-054329,INCB-54329|||INCB-54329
INCB054329, a structurally distinct bromodomain and extraterminal domain (BET) inhibitor, inhibits BRD2-BD1, BRD2-BD2, BRD3-BD1, BRD3-BD2, BRD4-BD1, BRD4-BD2, BRDT-BD1 and BRDT-BD2 with IC50 values of 44 nM, 5 nM, 9 nM, 1 nM, 28 nM, 3 nM, 119 nM and 63 nM respectively.
价 格：￥电议型 号：T22345产 地：中国大陆
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T1940BTB06584；化合物BTB06584BTB06584
BTB06584 is an IF1-dependent, selective inhibitor of the mitochondrial F1 Fo-ATPase. BTB06584 is a novel acetohydroxyacid synthase(AHAS) inhibitor, a promising drug target against Mycobacterium tuberculosis (MTB).
价 格：￥电议型 号：T1940产 地：中国大陆
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T19272DB04760 analog 1；化合物 T19272DB04760 analog 1
DB04760 analog 1 is an analogue of DB04760.
价 格：￥电议型 号：T19272产 地：中国大陆
