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T11297LFF-10101；化合物FF-10101FF-10101
FF-10101 is a potent inhibitor of FLT3.
价 格：￥电议型 号：T11297L产 地：中国大陆
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T11297FF-10101 succinate；化合物 T11297FF-10101 succinate
FF-10101 succinate is a potent FLT3 inhibitor.
价 格：￥电议型 号：T11297产 地：中国大陆
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T11296Flosulide；化合物 T11296ZK 38997|||CGP 28238；ZK 38997|||CGP 28238
Flosulide is an effective selective COX-2 inhibitor for the treatment of inflammatory diseases.
价 格：￥电议型 号：T11296产 地：中国大陆
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T11295Flibanserin-d4；化合物 T11295BIMT-17BS D4|||BIMT-17 D4|||Flibanserin D4；BIMT-17BS D4|||BIMT-17 D4|||Flib
Flibanserin, a compound identified as BIMT-17, acts as a complete agonist at the serotonin 5-HT1A receptor, with a binding affinity (Ki) of 1 nM, while functioning as an antagonist at the 5-HT2A receptor with a 49 nM affinity. Flibanserin D4 represents a deuterium-labeled version of Flibanserin.
价 格：￥电议型 号：T11295产 地：中国大陆
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T11294Flavanone hydrazone；化合物 T11294Flavanone hydrazone
Flavanone hydrazine is a potent non-steroidal anti-inflammatory agent that effectively inhibits lens protein-induced ocular inflammation.
价 格：￥电议型 号：T11294产 地：中国大陆
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T11293(±)-Fabesetron hydrochloride；化合物 T11293FK1052 hydrochloride；FK1052 hydrochloride
FK1052 hydrochloride is a potent 5-HT3 and 5-HT4 receptor dual antagonist.
价 格：￥电议型 号：T11293产 地：中国大陆
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T11292FKBP12 PROTAC dTAG-7；化合物 T11292dTAG-7；dTAG-7
FKBP12 PROTAC dTAG-7 (dTAG-7) is a heterobifunctional compound that selectively degrades the BET bromodomain transcriptional co-activator BRD4 by connecting BET bromodomains to the E3 ubiquitin ligase CRBN. Additionally, it serves as a degrader of FKBP12F36V when FKBP12F36V is expressed in-frame with a targeted protein.
价 格：￥电议型 号：T11292产 地：中国大陆
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T11291FKBP12 PROTAC dTAG-13；化合物 T11291dTAG-13；dTAG-13
FKBP12 PROTAC dTAG-13 (dTAG-13) is a degrader of FKBP12F36V with expression of FKBP12F36V in-frame with a protein of interest. FKBP12 PROTAC dTAG-13 (dTAG-13) also is a selective degrader of BET bromodomain transcriptional co-activator BRD4 by bridging BET bromodomains to an E3 ubiquitin ligase CRBN. FKBP12 PROTAC dTAG-13 (dTAG-13) is a PROTAC-based heterobifunctional degrader.
价 格：￥电议型 号：T11291产 地：中国大陆
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T11290FK-448 Free base；化合物 T11290FK-448 Free base
FK-448 Free base is an effective and specific inhibitor of chymotrypsin, with an IC50 of 720 nM.
价 格：￥电议型 号：T11290产 地：中国大陆
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T1129Benfotiamine苯磷硫胺Benzoylthiamine monophosphate|||S-Benzoylthiamine O-monophosphate|||苯磷硫胺
Benfotiamine (S-Benzoylthiamine O-monophosphate) is a synthetic S-acyl derivative of thiamine (vitamin B1), used as an antioxidant dietary supplement.
价 格：￥电议型 号：T1129产 地：中国大陆
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T11248Evogliptin tartrate；化合物 T11248DA-1229 tartrate；DA-1229 tartrate
Evogliptin tartrate has potential for anti-atherosclerosis therapy that targets arterial inflammation. Evogliptin tartrate is a potent, orally bioavailable and selective dipeptidyl peptidase-4 (DPP-4) inhibitor, with antidiabetic activity.
价 格：￥电议型 号：T11248产 地：中国大陆
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T11229Erlotinib-d6；化合物 T11229OSI-774 D6|||NSC 718781 D6|||CP-358774 D6；OSI-774 D6|||NSC 718781 D6|||CP-358
Erlotinib is a directly acting inhibitor EGFR tyrosine kinase inhibitor with an IC50 of 2 nM for human EGFR. Erlotinib D6 is a deuterium labeled Erlotinib .
价 格：￥电议型 号：T11229产 地：中国大陆
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T11188LEmixustat hydrochloride；化合物Emixustat hydrochlorideACU-4429 hydrochloride；ACU-4429 hydrochloride
Emixustat hydrochloride (ACU-4429 hydrochloride) strongly inhibits 11-cis-retinol production with IC50 values of 232 ± 3 nM. 11-cis-retinol Emixustat hydrochloride is a novel visual cycle modulator.
价 格：￥电议型 号：T11188L产 地：中国大陆
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T11188Emixustat；化合物 T11188ACU-4429；ACU-4429
Emixustat, is an inhibitor of the visual cycle isomerase with an IC50 value of 4.4 nM in vitro. a novel visual cycle modulator.
价 格：￥电议型 号：T11188产 地：中国大陆
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T11153EG00229；化合物 T11153EG00229
EG00229 is a neuropilin 1 (NRP1) receptor antagonist that selectively inhibits the binding of VEGF-A to the NRP1 b1 domain, achieving this inhibition with an IC50 value of 3 μM. It does not affect the binding of VEGF-A to other receptors, such as VEGFR-1 and VEGFR-2.
价 格：￥电议型 号：T11153产 地：中国大陆
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T11129LDuvelisib (R enantiomer) hydrochloride；杜韦利西布R对映体盐酸盐IPI-145 R enantiomer HCl|||Duvelisib (R enantiome
Duvelisib (R enantiomer) hydrochloride (INK1197 R enantiomer HCl) is a PI3K inhibitor. Duvelisib (R enantiomer) hydrochloride is the less active enantiomer of Duvelisib.
价 格：￥电议型 号：T11129L产 地：中国大陆
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T11129Duvelisib (R enantiomer)化合物Duvelisib R entiomerDuvelisib R enantiomer|||IPI-145 R enantiomer|||INK11
Duvelisib R enantiomer (IPI-145 R enantiomer) is an enantiomer of Duvelisib with lower activity. Duvelisib is a PI3K inhibitor.
价 格：￥电议型 号：T11129产 地：中国大陆
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T11095DREADD agonist 21 dihydrochloride；化合物 T11095DREADD agonist 21 dihydrochloride (56296-18-5 free base)
DREADD agonist 21 dihydrochloride is a potent human muscarinic acetylcholine M3 receptors ( hM3Dq ) agonist with EC 50 of 1.7 nM [1].
价 格：￥电议型 号：T11095产 地：中国大陆
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T11029hDHODH-IN-5；化合物hDHODH-IN-5DHODH-IN-7；DHODH-IN-7
hDHODH-IN-5 is an inhibitor of human dihydroorotate dehydrogenase (hDHODH, IC50 = 0.91 μM).
价 格：￥电议型 号：T11029产 地：中国大陆
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T1097Loratadine；氯雷他定SCH 29851|||Loratidine；氯雷他定|||SCH 29851|||Loratidine
Loratadine (SCH 29851) is a second-generation histamine H1 receptor antagonist used in the treatment of allergic rhinitis and urticaria. Unlike most classical antihistamines (HISTAMINE H1 ANTAGONISTS) it lacks central nervous system depressing effects such as drowsiness.
价 格：￥电议型 号：T1097产 地：中国大陆
