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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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T11179Elubrixin；化合物ElubrixinSB-656933；SB-656933
Elubrixin (SB-656933) inhibits neutrophil CD11b upregulation (IC50 of 260.7 nM) and shape change (IC50 of 310.5 nM). Elubrixin can be used for inflammatory diseases such as inflammatory bowel disease and airway inflammation. Elubrixin is a potent, selective, competitive, reversible and orally active CXCR2 antagonist and an IL-8 receptor antagonist.
价 格：￥电议型 号：T11179产 地：中国大陆
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T11174(R)-Elagolix；恶拉戈利NBI-56418；恶拉戈利|||NBI-56418
(R)-Elagolix (NBI-56418) is a short-acting, nonpeptide, GnRH antagonist with an IC50 and Ki of 0.25 and 3.7 nM, respectively. administered orally, that unlike injectable depot GnRH agonists and antagonists, produces a dose-dependent suppression of ovarian estrogen production, that is, from partial suppression at lower doses to full suppression at higher doses.
价 格：￥电议型 号：T11174产 地：中国大陆
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T1115Doxylamine succinate；琥珀酸多西拉敏Decapryn；琥珀酸多西拉敏|||Decapryn
Doxylamine Succinate is a pyridine derivate histamine H1 antagonist with pronounced sedative properties. Doxylamine succinate (Decapryn) competitively blocks the histamine H1 receptor and limits the typical allergic and anaphylactic responses, including bronchoconstriction, vasodilation, increased capillary permeability, and spasmodic contraction of the gastrointestinal smooth muscle, caused by actions of histamine on bronchial and gastrointestinal smooth muscles, and on capillaries. This drug a
价 格：￥电议型 号：T1115产 地：中国大陆
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T1114Ciclopirox olamine；环吡酮乙醇胺盐Ciclopirox ethanolamine；环吡酮乙醇胺盐|||环吡司胺|||Ciclopirox ethanolamine
Ciclopirox olamine is a broad-spectrum antifungal agent with additional antibacterial and anti-inflammatory activities.
价 格：￥电议型 号：T1114产 地：中国大陆
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T11135(E)-10-Hydroxynortriptyline maleate；化合物 T11135(E)-10-Hydroxy Nortriptyline maleate；(E)-10-Hydroxy No
(E)-10-Hydroxy Nortriptyline maleate, a metabolite of Nortriptyline, serves as a key active metabolite of the tricyclic antidepressant Amitriptyline, primarily utilized in alleviating depression symptoms.
价 格：￥电议型 号：T11135产 地：中国大陆
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T11128Dutogliptin；化合物 T11128PHX-1149 free base；PHX-1149 free base
Dutogliptin (PHX-1149 free base) is an oral, effective and selective dipeptide-peptide-4 (DPP4) inhibitor for the treatment of type 2 diabetes mellitus.
价 格：￥电议型 号：T11128产 地：中国大陆
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T11127Dutogliptin tartrate；化合物 T11127PHX-1149；PHX-1149
Dutogliptin tartrate is an effective and selective oral dipeptide-peptide-4 (DPP4) inhibitor for the treatment of type 2 diabetes mellitus.
价 格：￥电议型 号：T11127产 地：中国大陆
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T11125Durlobactam sodium salt；化合物Durlobactam钠盐ETX2514 sodium salt；杜巴坦|||ETX2514 sodium salt|||杜洛巴坦
Durlobactam sodium salt (ETX2514 sodium salt) is an inhibitor of β-lactamase with IC50 values of 4 nM, 14 nM, and 190 nM for Class A KPC-2, Class C AmpC, and Class D OXA-24, respectively. Durlobactam sodium salt can be used in studies about drug-resistant Gram-negative bacteria including Acinetobacter baumannii.
价 格：￥电议型 号：T11125产 地：中国大陆
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T11122-(Hydroxymethyl)pyridine吡啶甲醇吡啶甲醇|||Piconol
2-(Hydroxymethyl)pyridine (Piconol) is used as an organic synthesis and medicinal chemistry intermediate for the synthesis of the stimulant laxative bisacodyl, and as a pyridinol with hypoglycemic activity.
价 格：￥电议型 号：T1112产 地：中国大陆
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T11114Duloxetine metabolite Para-Naphthol Duloxetine；度洛西汀代谢物Para-Naphthol duloxetine；度洛西汀代谢物|||Para-Naphth
Para-Naphthol Duloxetine is a serotonin-norepinephrine reuptake inhibitor (SNRI),is a metabolite of Duloxetine.
价 格：￥电议型 号：T11114产 地：中国大陆
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T11113Duloxetine D3 hydrochloride；化合物 T11113(S)-Duloxetine D3 hydrochloride|||LY248686 D3 hydrochloride；(S
Duloxetine D3 hydrochloride is a serotonin-norepinephrine reuptake inhibitor (SNRI) with a Ki of 4.6 nM, used for treatment of major depressive disorder and generalized anxiety disorder (GAD).Duloxetine D3 hydrochloride ((S)-Duloxetine D3 hydrochloride) is a deuterium labeled Duloxetine hydrochloride.
价 格：￥电议型 号：T11113产 地：中国大陆
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T1111Pralidoxime Chloride吡啶醛肟甲氯2-PAM chloride|||吡啶醛肟甲氯|||2-Pyridinealdoxime methochloride|||2-PAM (chlori
Pralidoxime Chloride (2-PAM chloride) is a useful agent in the treatment of organophosphate poisoning. Pralidoxime binds to organophosphate-inactivated acetylcholinesterase, used to combat poisoning by organophosphates or acetylcholinesterase inhibitors (nerve agents).
价 格：￥电议型 号：T1111产 地：中国大陆
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T11099Droxicainide；羟卡尼Droxicainide
Droxicainide is an antiarrhythmic agent.
价 格：￥电议型 号：T11099产 地：中国大陆
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T11098Droloxifene；屈洛昔芬3-Hydroxytamoxifen；3-Hydroxytamoxifen
Droloxifene (3-Hydroxytamoxifen), a tamoxifen derivative, is an oral active and selective estrogen receptor modulator.Droloxifene induced p53 expression and apoptosis in McF-7 cells.Fluroxifene has anti-estrogen and anti-implantation effects.Fluroxifene prevented bone loss in ovariectomized rats.
价 格：￥电议型 号：T11098产 地：中国大陆
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T11092DPBQ；化合物DPBQZINC1620467|||2,3-Diphenylbenzo[g]quinoxaline-5,10-dione；ZINC1620467|||2,3-Diphenylbenzo
DPBQ (ZINC1620467) is a p53 activator. DPBQ could activate p53 and trigger apoptosis in a polyploid-specific manner, without inhibition of topoisomerase or bind DNA.
价 格：￥电议型 号：T11092产 地：中国大陆
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T11090L1Aldoxorubicin hydrochloride；化合物Aldoxorubicin盐酸盐Aldoxorubicin hydrochloride (1361644-26-9 Free base）；
Aldoxorubicin hydrochloride is an albumin-binding prodrug of Doxorubicin, a DNA topoisomerase II inhibitor. Aldoxorubicin hydrochloride is released from albumin under acidic conditions. Aldoxorubicin hydrochloride exhibits potent antitumor activities in various cancer cell lines and in murine tumor models.
价 格：￥电议型 号：T11090L1产 地：中国大陆
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T11090LAldoxorubicin；化合物 T11090LDOXO-EMCH|||INNO-206；DOXO-EMCH|||INNO-206
Aldoxorubicin has effective antitumor activities in various cancer cell lines and in murine tumor models. Aldoxorubicin is an albumin-binding prodrug of Doxorubicin (DNA topoisomerase II inhibitors).
价 格：￥电议型 号：T11090L产 地：中国大陆
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T11090MC-DOXHZN；化合物 T11090Doxorubicin(6-maleimidocaproyl)hydrazone；Doxorubicin(6-maleimidocaproyl)hydrazon
Mc-doxhzn is a protein-binding prodrug of DOXUbicin (DNA topoisomerase II inhibitor) with acid sensitivity.
价 格：￥电议型 号：T11090产 地：中国大陆
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T11089Doxercalciferol-D3；化合物 T11089Doxercalciferol-D3
Doxercalciferol-d3 is the deuterated form of Doxercalciferol and ACTS as vitamin D receptor activator (VDRA), which is a vitamin D2 analogue.
价 格：￥电议型 号：T11089产 地：中国大陆
