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T1433Ritodrine hydrochloride；盐酸利托君DU21220|||Ritodrine HCl|||NSC 291565；DU21220|||盐酸利托君|||Ritodrine HCl|||
Ritodrine hydrochloride (NSC 291565) binds to and activates beta-2 adrenergic receptors of myometrial cells in the uterus, which decreases the intensity and frequency of uterine contractions. Ritodrine hydrochloride (NSC 291565) is a phenethylamine derivative with tocolytic activity. Specifically, Ritodrine hydrochloride (NSC 291565) probably activates adenyl cyclase, thereby increasing production of cyclic adenosine monophosphate (cAMP), which in turn enhances the efflux of calcium from vasc
价 格：￥电议型 号：T1433产 地：中国大陆
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T14320ARL67156 trisodium salt；化合物 T14320ARL67156 trisodium salt
ARL 67156 is a weak competitive inhibitor of NTPDase1 (CD39), NTPDase3 and NPP1, with Kis of 11, 18 and 12 μM, respectively[1]. ARL67156 trisodium salt is an inhibitor of ecto-ATPase.
价 格：￥电议型 号：T14320产 地：中国大陆
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T14305Apicidin；化合物 ApicidinOSI 2040；OSI 2040
Apicidin (OSI 2040) is a histone deacetylase (HDAC) inhibitor with antiparasitic activity and antiproliferative activity.Apicidin attenuates memory deficits, inhibits cell growth and proliferation, and induces apoptosis and autophagy by decreasing Abeta load in APP/PS1 mice, and can be used to study leukemia.
价 格：￥电议型 号：T14305产 地：中国大陆
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T14299AP20187；化合物AP20187B/B Homodimerizer；B/B Homodimerizer
AP20187 (B/B Homodimerizer) is a cell-permeable compound employed to dimerize FK506-binding protein (FKBP) fusion proteins, thereby initiating biological signaling cascades, gene expression, or disrupting protein-protein interactions.
价 格：￥电议型 号：T14299产 地：中国大陆
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T1428Trifluridine；曲氟尿苷NSC 529182|||Trifluorothymidine|||5-Trifluorothymidine|||NSC 75520|||Viroptic|||Tri
Trifluridine (NSC-75520) is a fluorinated thymidine analog with potential antineoplastic activity. Trifluridine is incorporated into DNA and inhibits thymidylate synthase, resulting in inhibition of DNA synthesis, inhibition of protein synthesis, and apoptosis. This agent also exhibits antiviral activity.
价 格：￥电议型 号：T1428产 地：中国大陆
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T14220Amine-PEG3-Biotin；化合物Amine-PEG3-BiotinAmine-PEG3-Biotin
Amine-PEG3-Biotin can be used as a signal amplification label.
价 格：￥电议型 号：T14220产 地：中国大陆
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T14209Amebucort；安布可特Amebucort
Amebucort is a synthetic glucocorticoid corticosteroid. It may used for the research of inflammatory disorders.
价 格：￥电议型 号：T14209产 地：中国大陆
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T14208AMD 3465；化合物 T14208GENZ-644494；GENZ-644494
AMD 3465 also potently inhibits the replication of X4 HIV strains (IC50: 1-10 nM). However, it has no effect on CCR5-using (R5) viruses. AMD 3465 (GENZ-644494) is a potent antagonist of CXCR4, inhibits binding of 12G5 mAb and CXCL12AF647 to CXCR4, with IC50s of 0.75 nM and 18 nM in SupT1 cells.
价 格：￥电议型 号：T14208产 地：中国大陆
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T14207Amcinafal；安西法尔SQ 15102；安西法尔|||SQ 15102
Amcinafal is an active diol,and used against virus replication and interferon production.
价 格：￥电议型 号：T14207产 地：中国大陆
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T14206Ambutonium bromide；化合物 T14206BL700；BL700
Ambutonium bromide is an antagonist of acetylcholine.
价 格：￥电议型 号：T14206产 地：中国大陆
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T14205AM679；化合物 T14205AM679
AM679 is a potent and selective FLAP inhibitor with IC50s of 2.2 nM/0.6 nM/154 nM for FLAP binding/hLA/hWB respectively. IC50 value: 2.2 nM/0.6 nM/154 nM(FLAP binding/hLA/hWB) [1] AM679 showed an improved CYP inhibition profile (IC50 3A4 = 16.7 lM, 2C9 = 3.7 lM, 2D6 >30 lM), no time dependent inhibition against CYP3A4 (0.003 min-1 vs 0.057 min-1 for troleandomycin control 10 uM) and no CYP3A4 induction. AM679 has an excellent hWB IC50 potency of 154 nM. Target: FLAP in vitro: AM679 showed excell
价 格：￥电议型 号：T14205产 地：中国大陆
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T14203AM-8735；化合物 T14203AM-8735
AM-8735 is an inhibitor of MDM2 ( IC50: 25 nM).
价 格：￥电议型 号：T14203产 地：中国大陆
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T14202AM-4668；化合物 T14202AM-4668
AM-4668 is a type 2 diabetes GPR40 agonist. For GPR40, in A9 cells (GPR40 IP3 assay) and CHO cells (GPR40 aequorin assay), the EC50s are 3.6 nM and 36 nM, respectively.
价 格：￥电议型 号：T14202产 地：中国大陆
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T14201AM-2099；化合物 T14201AM-2099
AM-2099 is a voltage-gated sodium channel Nav1.7 inhibitor (IC50: 0.16 μM).
价 格：￥电议型 号：T14201产 地：中国大陆
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T14200AM-1638；化合物 T14200AM-1638
AM-1638 is a full agonist of GPR40/FFA1 (EC50: 0.16 μM).
价 格：￥电议型 号：T14200产 地：中国大陆
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T1420Diethylcarbamazine citrate；枸橼酸乙胺嗪Caritrol|||Loxuran|||Dicarocide；Caritrol|||枸橼酸乙胺嗪|||Loxuran|||Dicar
Diethylcarbamazine citrate (Caritrol) is an anthelmintic used primarily as the citrate in the treatment of filariasis, particular infestations with Wucheria bancrofti or Loa loa. It is an inhibitor of arachidonic acid metabolism in filarial microfilaria.
价 格：￥电议型 号：T1420产 地：中国大陆
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T14147Pelitrexol；化合物 T14147AG 2037；AG 2037
Pelitrexol (AG 2037) is a glycinamide ribonucleotide formyltransferase (GARFT) inhibitor.
价 格：￥电议型 号：T14147产 地：中国大陆
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T14145AGN194204；化合物 T14145IRX4204|||NRX194204|||VTP 194204；IRX4204|||NRX194204|||VTP 194204
AGN194204 (IRX4204) is inactive against RAR and is an orally active and selective RXR agonist with Kd values 0.4 nM, 3.6 nM and 3.8 nM and EC50s of 0.2 nM, 0.8 nM and 0.08 nM for RXRα, RXRβ and RXRγ, respectively. AGN194204 has anti-inflammatory and anticarcinogenic actions[1][2].
价 格：￥电议型 号：T14145产 地：中国大陆
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T14134Afabicin；化合物 T14134AFN-1720|||Debio 1450；AFN-1720|||Debio 1450
Afabicin is the prodrug of Debio1452. Debio1452 is an inhibitor FabI, an enzyme critical to fatty acid biosynthesis in staphylococci.
价 格：￥电议型 号：T14134产 地：中国大陆
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T14120ACT-709478；化合物 T14120ACT-709478
ACT-709478 is a potent, selective T-type calcium channel blocker that is orally active and capable of penetrating the brain. It is currently utilized in research focusing on generalized epilepsies[1].
价 格：￥电议型 号：T14120产 地：中国大陆
