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T1549Raloxifene hydrochloride；盐酸雷洛昔芬LY156758 hydrochloride|||Raloxifene HCl|||LY139481 hydrochloride|||Ke
Raloxifene hydrochloride (LY156758 hydrochloride) is a second generation selective estrogen receptor modulator (SERM) used to prevent osteoporosis in postmenopausal women. It has estrogen agonist effects on bone and cholesterol metabolism but behaves as a complete estrogen antagonist on mammary gland and uterine tissue.
价 格：￥电议型 号：T1549产 地：中国大陆
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T1534Darifenacin hydrobromide；氢溴酸达非那新Darifenacin HBr|||UK-88525；氢溴酸达非那新|||Darifenacin HBr|||UK-88525
Darifenacin hydrobromide (UK-88525) is a selective muscarinic receptor antagonist used to treat urinary incontinence and overactive bladder syndrome.
价 格：￥电议型 号：T1534产 地：中国大陆
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T15300Fluorofenidone；化合物FluorofenidoneAKF-PD；AKF-PD
Fluorofenidone (AKF-PD) attenuates the progression of renal interstitial fibrosis partly by suppressing NADPH oxidase and extracellular matrix (ECM) deposition via the PI3K/Akt signalling pathway. Fluorofenidone is an analogue of AMR69. Which displays equivalent lower toxicity, antifibrotic activity, and longer half-life.
价 格：￥电议型 号：T15300产 地：中国大陆
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T15278Fezolinetant；化合物FezolinetantESN-364；ESN-364
Fezolinetant (ESN-364) is an antagonist of the neurokinin 3 receptor (NK3R). It is used for the treatment of menopausal hot flushes.
价 格：￥电议型 号：T15278产 地：中国大陆
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T15277Fervenulin；热诚菌素Fervenulin
Fervenulin is isolated from a nematicidal actinomycete Streptomyces sp. CMU-MH021 has nematicidal activity. CMU-MH021 inhibits egg hatch(MICs: 30 μg/mL) and J2 mortality(MICs: 120 μg/mL) of M. incognita.
价 格：￥电议型 号：T15277产 地：中国大陆
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T15276Ferroquine；二茂铁氯喹SSR97193|||Ferrochloroquine；SSR97193|||Ferrochloroquine
Ferroquine (Ferrochloroquine) is a ferrocenyl analogue of Chloroquine with antimalarial activity. Ferroquine induces oxidative stress and the subsequent destruction of the membrane, resulting in parasiticidal effect on Plasmodium.
价 格：￥电议型 号：T15276产 地：中国大陆
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T15275Fenobam；非诺班Fenobam
Fenobam shows inverse agonist activity which blocks the mGlu5 receptor basal activity(IC50: 84 nM). Fenobam has anxiolytic activity. Fenobam is a selective and non-competitive mGluR5 antagonist acting at an allosteric modulatory site (Kd values are 54 and 31 nM for rat and human recombinant mGlu5 receptors, respectively).
价 格：￥电议型 号：T15275产 地：中国大陆
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T15274FEN1-IN-1；化合物FEN1-IN-1LNT-1；LNT-1
FEN1-IN-1 (LNT-1) is an inhibitor of flap endonuclease 1 (FEN1). FEN1-IN-1 binds to the active site of FEN1. It partly achieves inhibition by the co-ordination of Mg2+ ions.
价 格：￥电议型 号：T15274产 地：中国大陆
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T15273Fedovapagon；非多伐贡VA483|||A106483；VA483|||A106483
Fedovapagon (VA106483) is a selective and potent agonist of the vasopressin V2 receptor (V2R) that inhibits the growth of intersegmental vessels in zebrafish. Fedovapagon can be used to study overactive bladder, nocturia, and painful bladder syndromes.
价 格：￥电议型 号：T15273产 地：中国大陆
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T15272Febantel；苯硫胍Febantel
Febantel is an anthelmintic. It is used for veterinary use on dogs, cats, cattle, sheep, goats, pig, and poultry against roundworms and tapeworms.
价 格：￥电议型 号：T15272产 地：中国大陆
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T15186(E)-4-Hydroxytamoxifen；(E)-4-羟基他莫昔芬(E)-4-Hydroxytamoxifen
(E)-4-Hydroxytamoxifen is a less active isomer of (Z)-4-hydroxytamoxifen and also is an estrogen receptor modulator.
价 格：￥电议型 号：T15186产 地：中国大陆
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T1516Curcumin；姜黄素Diferuloylmethane|||Natural Yellow 3|||Indian Saffron|||Turmeric yellow；Diferuloylmethan
Curcumin (Natural Yellow 3) is a phenolic natural product, an inhibitor of histone acetyltransferase p300/CREB (IC50=25 μM) with specificity. Curcumin has a wide range of pharmacological activities such as antitumor, anti-inflammatory and antioxidant.
价 格：￥电议型 号：T1516产 地：中国大陆
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T15135LDirect Black 38 free acid；化合物 T15135LNSC8679|||Ferristatin II；NSC8679|||Ferristatin II
Ferristatin II (Direct Black 38 free acid) is a polysulphonated dye and promotes the degradation of transferrin receptor-1 in vitro and in vivo.
价 格：￥电议型 号：T15135L产 地：中国大陆
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T14928Agerafenib hydrochloride；化合物 T14928RXDX-105 hydrochloride|||CEP-32496 (hydrochloride)；RXDX-105 hydro
Agerafenib hydrochloride is a highly potent inhibitor of BRAFV600E (Kd: 14 nM).
价 格：￥电议型 号：T14928产 地：中国大陆
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T14885CBS9106；化合物 CBS9106Felezonexor|||SL-801；Felezonexor|||SL-801
CBS9106 (SL-801) is a reversible oral CRM1 inhibitor with CRM1 degrading and antitumor activity.CBS9106 inhibits CRM1-dependent nuclear export and reduces CRM1 protein levels.CBS9106 inhibits tumor growth and prolongs the survival of mice bearing tumor xenografts.CBS9106 is an inhibitor of CRM1-dependent nuclear export and reduces CRM1 protein levels.
价 格：￥电议型 号：T14885产 地：中国大陆
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T14883Idoxifene；化合物 T14883CB7432；CB7432
Idoxifene is a tissue-specific selective estrogen receptor modulator.
价 格：￥电议型 号：T14883产 地：中国大陆
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T1475Fesoterodine fumarate；富马酸非索罗定Toviaz|||SPM 907；Toviaz|||SPM 907|||富马酸非索罗定
Fesoterodine fumarate (Toviaz) is the fumarate salt form of fesoterodine, a competitive muscarinic receptor antagonist with muscle relaxant and urinary antispasmodic properties. Fesoterodine is rapidly hydrolyzed in vivo into its active metabolite 5-hydroxymethyl tolterodine, which binds and inhibits muscarinic receptors on the bladder detrusor muscle, thereby preventing bladder contractions or spasms caused by acetylcholine.
价 格：￥电议型 号：T1475产 地：中国大陆
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T1470LFexofenadine hydrochloride；盐酸非索非那定Fexofenadine hydrochloride
Fexofenadine Hydrochloride is a carboxylated metabolic derivative of terfenadine and long-lasting selective histamine H1 receptor antagonist, with antihistaminic activity.
价 格：￥电议型 号：T1470L产 地：中国大陆
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T1470Fexofenadine hydrochloride；盐酸非索非那定Terfenidine carboxylate hydrochloride|||MDL-16455 hydrochloride|||
Fexofenadine hydrochloride (Terfenidine carboxylate hydrochloride) is a second generation antihistamine that is used for the treatment of allergic rhinitis, angioedema and chronic urticaria.
价 格：￥电议型 号：T1470产 地：中国大陆
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T14571Bifenazate；化合物BifenazateBifenazate
Bifenazate is a positive allosteric modulator of GABA receptor. Bifenazate is an acaricide that controls 100% of mites at a concentration of 25 ppm.
价 格：￥电议型 号：T14571产 地：中国大陆
