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T11302Flumexadol；化合物 T11302Flumexadol
Flumexadol is a selective and affinity 5-HT2C receptor agonist with a Ki of 25 nM for the (+)-enantiomer of Flumexadol, and is 40-fold selective over the 5-HT2A receptor. Flumexadol is an orally active non-narcotic analgesic.
价 格：￥电议型 号：T11302产 地：中国大陆
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T11301LFlomoxef sodium；氟氧头孢钠Flomoxef sodium
Flomoxef sodium, an antibiotic belonging to the oxacephem group, exhibits excellent activity against a broad spectrum of Gram-positive bacteria.
价 格：￥电议型 号：T11301L产 地：中国大陆
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T11301Flomoxef；氟氧头孢Flomoxef
Flomoxef is an antibiotic in oxacephem group and has excellent activity against various gram-positive bacteria.
价 格：￥电议型 号：T11301产 地：中国大陆
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T11299FLT3-IN-4；化合物FLT3-IN-4FLT3 inhibitor 9u；FLT3 inhibitor 9u
FLT3-IN-4 (FLT3 inhibitor 9u) is a potent and orally effective Fms-like tyrosine receptor kinase 3 (FLT3;?IC50=7 nM) inhibitor ,for treating acute myelogenous leukemia.
价 格：￥电议型 号：T11299产 地：中国大陆
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T11298FLT3-IN-3；化合物FLT3-IN-3FLT3-IN-3
FLT3-IN-3 is an effective FLT3 inhibitor, and the IC50s of FLT3 WT and FLT3 D835Y are 13 and 8 nM, respectively.
价 格：￥电议型 号：T11298产 地：中国大陆
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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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T1128L(S)-Oxiracetam；化合物 T1128L(S)-ISF-2522|||S-Oxiracetam；(S)-ISF-2522|||S-Oxiracetam
(S)-Oxiracetam is a positive allosteric the AMPA receptorsmodulator.
价 格：￥电议型 号：T1128L产 地：中国大陆
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T11289Finafloxacin；非那沙星Finafloxacin
Finafloxacin, a fluoroquinolone antimicrobial agent from a new 8-cyano subclass, is most effective in slightly acidic environments (pH 5.0-6.0), a condition where other fluoroquinolones typically reduce in activity. It selectively targets bacterial type II topoisomerases, such as DNA gyrase and DNA topoisomerase IV, making it suitable for treating serious bacterial infections particularly in acidic contexts, including urinary tract infections (UTIs) and Helicobacter pylori infections.
价 格：￥电议型 号：T11289产 地：中国大陆
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T11288Filipin III；菲律宾菌素 IIIFilipin III
Filipin III is extracted from strain KPE18H and has significant antifungal activity.
价 格：￥电议型 号：T11288产 地：中国大陆
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T11287Filipin complex；菲律宾菌素复合体Filipin complex
Filipin complex is a 28-membered cyclopentene macrolide antifungal antibiotic produced by a mixture of S. filipinensis, S. avermitilis, and S. miharaensis that inhibits the entry of PRRSV viruses into cells.
价 格：￥电议型 号：T11287产 地：中国大陆
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T11286Fiduxosin；非多唑嗪A 185980.1|||ABT 980；A 185980.1|||ABT 980
Fiduxosin is a selective and potent α1-adrenoceptor antagonist with inhibitory effects on α1a-adrenoceptor, α1b-adrenoceptor and α1d-adrenoceptor, with Ki values of 0.160 nM, 24.9 nM and 0.920 nM, respectively. Fiduxosin can be used for the treatment of benign prostatic hyperplasia.
价 格：￥电议型 号：T11286产 地：中国大陆
