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T11339Furegrelate sodium；化合物Furegrelate sodiumU-63557A；U-63557A
Furegrelate sodium (U-63557A) is a selective thromboxane synthase inhibitor with oral activity. Furegrelate sodium(U-63557A) inhibits thromboxane A2 (TXA2) synthase in human platelet microsomes with an IC50 of 15 nM.
价 格：￥电议型 号：T11339产 地：中国大陆
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T11338Furamidine；化合物 T11338DB75|||NSC 305831；DB75|||NSC 305831
Furamidine is also a selective and cell-permeable protein arginine methyltransferase 1 (PRMT1) inhibitor with an IC50 of 9.4 μM. Furamidine is selective for PRMT1 over PRMT5, PRMT6, and PRMT4 (CARM1) (IC50s of 166 μM, 283 μM, and >400 μM, respectively). Furamidine (DB75) is abisbenzamidine derivative and an antiparasite agent. Furamidine is a potent, reversible and competitive tyrosyl-DNA phosphodiesterase 1 (TDP-1) inhibitor. Inhibition of TDP-1 by Furamidine is effective both with single- and
价 格：￥电议型 号：T11338产 地：中国大陆
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T11337Fumarate hydratase-IN-1；Fumarate hydratase 抑制剂1Fumarate hydratase-IN-1
Fumarate hydratase-IN-1 is a cell-permeable fumarate hydratase inhibitor with antiproliferative activity and can be used to study cellular activity.
价 格：￥电议型 号：T11337产 地：中国大陆
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T11336Fumarate hydratase-IN-2 sodium salt化合物 T11336Fumarate hydrataseIN2 sodium salt|||Fumarate hydratase
Fumarate hydratase-IN-2 sodium salt (compound 3) is a cell-permeable and competitive fumarate hydratase inhibitor ( K i =4.5 μM). Fumarate hydratase-IN-2 sodium salt has nutrient-dependent cytotoxicity [1].
价 格：￥电议型 号：T11336产 地：中国大陆
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T11335Fulvestrant (S enantiomer)；化合物 T11335ZM 182780 S enantiomer|||ICI 182780 S enantiomer|||Fulvestrant
Fulvestrant S enantiomer is the less active S enantiomer of Fulvestrant. Fulvestrant is a potent estrogen receptor antagonist with an IC50 of 9.4 nM.
价 格：￥电议型 号：T11335产 地：中国大陆
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T11334Fulvestrant (R enantiomer)；化合物 T11334ICI 182780 R enantiomer|||ZD 9238 R enantiomer|||ZM 182780 R en
Fulvestrant R enantiomer is the less active R enantiomer of Fulvestrant. Fulvestrant is a potent estrogen receptor antagonist with an IC50 of 9.4 nM.
价 格：￥电议型 号：T11334产 地：中国大陆
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T11333Fulvene-5；化合物 T11333Fulvene-5
Fulvene-5 is a chemical compound that exhibits antitumor activity. It functions as a potent inhibitor of NADPH oxidase 4 (NOX4) and possesses antioxidant properties. Additionally, Fulvene-5 acts as a reactive oxygen species (ROS) modifying agent and a powerful radioprotector.
价 格：￥电议型 号：T11333产 地：中国大陆
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T11332FUBP1-IN-1；化合物 T11332FUBP1–IN-1；FUBP1–IN-1
FUBP1 - in-1, with an IC50 value of 11.0 M, is an effective FUSE binding protein 1 (FUBP1) inhibitor that can interfere with the binding of FUBP1 to its SINGLE-strand target DNA FUSE sequence.
价 格：￥电议型 号：T11332产 地：中国大陆
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T11331LFTI 276；化合物 T11331LFTI 276
FTI-276 is an inhibitor of protein farnesyltransferase (PFT) (IC50s: 0.9 and 0.5 nM for Plasmodium falciparum and human).
价 格：￥电议型 号：T11331L产 地：中国大陆
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T11331FTI 276 TFA；化合物 T11331FTI 276 TFA
FTI 276 TFA is effective against plasmodium falciparum and humans.It is a protein-based nikyltransferase (PFT) inhibitor with an IC50s of 0.9 nM and 0.5 nM, respectively.
价 格：￥电议型 号：T11331产 地：中国大陆
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T11330LFTI-2148；化合物 T11330LFTI-2148
FTI-2148 is an inhibitor of RAS C-terminal mimetic dual farnesyl transferase (FT-1) and geranylgeranyl transferase-1 (GGT-1) (IC50s: 1.4 nM and 1.7 μM, respectively).
价 格：￥电议型 号：T11330L产 地：中国大陆
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T11330FTI-2148 diTFA；化合物 T11330FTI-2148 diTFA
FTI-2148 diTFA, a dual inhibitor targeting both farnesyl transferase (FT-1) and geranylgeranyl transferase-1 (GGT-1), functions as a RAS C-terminal mimetic. It exhibits potent inhibitory capabilities with IC50 values of 1.4 nM for FT-1 and 1.7 μM for GGT-1, respectively.
价 格：￥电议型 号：T11330产 地：中国大陆
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T11329FT895；化合物FT895FT895
FT895 is a selective and potent HDAC11 inhibitor with antifungal and antitumor activity that inhibits HDAC11 expression and limits EV71 replication in vitro.
价 格：￥电议型 号：T11329产 地：中国大陆
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T11328FT-1518；化合物 T11328FT-1518
FT-1518 ,exhibits antitumor activity, is a new generation selective, potent and oral bioavailable mTORC1 and mTORC2 inhibitor.
价 格：￥电议型 号：T11328产 地：中国大陆
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T11327LFR 167653 free base；化合物 T11327LFR 167653 free base
FR 167653 free base is an orally active p38 MAPK inhibitor and is effective in treating inflammation, relieving trauma, and ischemia-reperfusion injury in vivo. It also is a potent suppressor of TNF-α and IL-1β production via specific inhibition of p38 MAPK activity.
价 格：￥电议型 号：T11327L产 地：中国大陆
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T11326Frovatriptan succinate hydrate；夫罗曲坦琥珀酸盐水合物u00A0Frovelan|||Frova；Frovelan|||夫罗曲坦琥珀酸盐水合物u00A0|||Frova
Frovatriptan succinate hydrate (Frova) is effective in treating the full spectrum of migraine including the associated symptoms of nausea, vomiting, photophobia, and phonophobia. Frovatriptan succinate hydrate can also be used as in mini-prophylaxis in menstrual migraine.?Frovatriptan succinate hydrate is a potent, high affinity, selective and orally active 5-HT1B, HT1D receptor agonist and a moderately potent 5-HT7 receptor agonist, with pKi values of 8.6, 8.4, and 6.7, respectively.
价 格：￥电议型 号：T11326产 地：中国大陆
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T11325Frondoside A；化合物 T11325Frondoside A
possesses anticancer, anti-invasive, anti-metastasis, anti-angiogenic and pro-apoptosis properties with high safety.Frondoside A, a natural glycoside extracted from the sea cucumber, Cucumaria frondosa,
价 格：￥电议型 号：T11325产 地：中国大陆
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T11324FRG8701；化合物 T11324FRG8701
FRG8701 is a new Histamine H2-receptor antagonist with an IC50 of ranging from 0.25 to 0.43 μM.
价 格：￥电议型 号：T11324产 地：中国大陆
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T11323LFrakefamide；化合物 T11323LFrakefamide
Frakefamide is a potent analgesic that functions as a peripheral active μ-selective receptor agonist. It cannot penetrate the blood-brain barrier to enter the central nervous system.
价 格：￥电议型 号：T11323L产 地：中国大陆
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T11323Frakefamide TFA (188196-22-7 free base)；化合物 T11323Frakefamide TFA；Frakefamide TFA
Frakefamide is unable to penetrate the blood-brain-barrier and enter the central nervous system. Frakefamide TFA is a potent analgesic that acts as a peripheral active μ-selective receptor agonist.
价 格：￥电议型 号：T11323产 地：中国大陆
