5-HT Receptor(5-羟色胺受体)
5-HT receptor (5-hydroxytryptamine receptors) is a group of GPCRs (G protein-coupled receptors) and LGICs (ligand-gated ion channels) found in the central and peripheral nervous systems.
Products for 5-HT Receptor
- Cat.No. 产品名称 Information
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GC73217
FFN246
FFN246是血清素转运蛋白(SERT)探针和水疱单胺转运蛋白2 (VMAT2)的荧光双底物,激发和发射光谱为392/427 nm。
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GC31011
FK1052 hydrochloride
(±)-FK1052
FK1052 hydrochloride ((±)-FK1052) 是 Fabesetron hydrochloride 的消旋体,是一种有效的 5-HT3 和 5-HT4 受体双重拮抗剂。 -
GC60846
Flesinoxan
氟辛克生
Flesinoxan是一种降压剂,是一种有效的,高亲和力的选择性的5-羟色胺1A(5-HT1A)受体激动剂,EC50值为24nM。Flesinoxan还具有有效的抗焦虑/抗抑郁作用。 -
GC11100
Flibanserin
氟立班丝氨; BIMT-17; BIMT-17BS
A 5-HT1A receptor agonist and 5-HT2A receptor antagonist -
GC74179
Flibanserin hydrochloride (propan-2-ol) hydrate
盐酸氟立班丝氨; BIMT-17 hydrochloride (propan-2-ol) hydrate; BIMT-17BS hydrochloride (propan-2-ol) hydrate
Flibanserin hydrochloride (propan-2-ol) hydrateKi值分别为1nM和49nM的口服活性血清素5-HT1A受体激动剂和5-HT2A受体拮抗剂。 -
GC68364
Flibanserin-d4-1
BIMT-17-d4-1; BIMT-17BS-d4-1
Flibanserin-d4-1 是 Flibanserin 氘代物。Flibanserin (BIMT-17) 是 5-羟色胺 (5-HT1A) 受体 (Ki=1 nM) 的完全激动剂和 5-HT2A 拮抗剂 (49 nM)。Flibanserin 与多巴胺 D4 受体 (Ki=4-24 nM) 结合,对多种其他神经递质受体和离子通道的亲和力可忽略不计。Flibanserin 有潜力用于性欲减退 (HSDD)的研究。 -
GC12535
Flopropione
夫洛丙酮
Flopropione 是一种 5-HT 受体拮抗剂,也是一种儿茶酚-邻甲基转移酶 (COMT) 抑制剂。 -
GC38912
Flumexadol
氟甲沙朵
Flumexadol 是一种口服活性非麻醉镇痛药。Flumexadol 是一种选择性和亲和力的 5-HT2C 受体激动剂,对于 Flumexadol 的 (+)-对映体,Ki 为 25 nM,选择性是 5-HT2A 受体的 40 倍。 -
GC11709
Fluoxetine HCl
盐酸氟西汀; LY 110140
An Analytical Reference Material -
GC13092
Fluvoxamine
氟伏沙明; DU-23000
A selective serotonin reuptake inhibitor -
GC15025
Fluvoxamine maleate
氟伏沙明马来酸盐; DU-23000 maleate
A selective serotonin reuptake inhibitor -
GC73914
FPT
FPT2-氨基四氢萘是5-HT1AR的有效部分激动剂,5-HT1BR和5-HT1DR的完全激动剂,EC50s分别为39.3 nM、1.2 nM、0.5 nM。
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GC25434
Frovatriptan Succinate
SB 209509 Succinate,VML 251 Succinate
Frovatriptan Succinate(SB 209509 Succinate,VML 251 Succinate) is the succinate salt form of frovatriptan, a synthetic triptan with serotonin (5-HT) receptor agonist activity especially for the 5-HT1B/1D receptors. -
GC38781
Frovatriptan succinate hydrate
罗曲普坦琥珀酸盐,(R)-Frovatriptan succinate hydrate; SB 209509 succinate hydrate; VML 251 succinate hydrate
An agonist of 5-HT1B and 5-HT1D receptors -
GC38227
Gamma-Mangostin
γ-倒捻子素,γ-Mangostin
A xanthone with diverse biological activities -
GC38529
Geissoschizine methyl ether
缝籽木嗪甲醚
Geissoschizine methyl ether,一种 Uncaria hook 发现的生物碱类化合物,也是具有精神药物作用的 Yokukansan 的主要活性成分。Geissoschizine methyl ether 是有效的 5-HT1A 受体的激动剂。 -
GC70532
Gepirone-d8
Gepirone-d8是氘标记的吉皮隆。
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GC11624
GR 113808
GR 113808是一种有效和选择性的5-HT4受体拮抗剂,pKb=8.8。
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GC61464
GR 125743
GR125743是一种选择性的5-HT1B/1D受体拮抗剂,与野生型的人h5-HT1B和5-HT1D结合的pKi分别为8.85和8.31。GR125743可用于帕金森病和心血管疾病的研究。
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GC74636
GR 55562 hydrochloride
GR 55562 hydrochloride是一种选择性5-HT1B受体拮抗剂。
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GC12398
Granisetron
格拉司琼; BRL 43694
Granisetron (BRL 43694) 是一种血清素 5-HT3 受体拮抗剂,用作止吐剂,用于治疗化疗后的恶心和呕吐。 -
GC16029
Granisetron HCl
盐酸格拉司琼; BRL 43694A
A 5-HT3 receptor antagonist with antiemetic activity -
GC19176
GSK163090
GSK163090 是一种有效的、选择性的和具有口服活性的 5-HT1A/1B/1D 受体拮抗剂,pKi 值分别为 9.4/8.5/9.7。
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GC30762
Harmine (Telepathine)
去氢骆驼蓬碱; Telepathine
A unique regulator of PPARγ expression -
GC38413
Harmine hydrochloride
哈尔碱盐酸盐(水合),Telepathine hydrochloride
A unique regulator of PPARγ expression -
GC60915
Hydroxy ziprasidone
齐拉西酮羟基化杂质
Hydroxyziprasidone是Ziprasidone的杂质。Ziprasidone,一种抗精神药物,是5-HT和多巴胺(dopaminereceptor)受体拮抗剂。 -
GC36291
Idalopirdine
Lu AE58054
A 5-HT6 receptor antagonist -
GC63015
Iferanserin
S-MPEC
Iferanserin (S-MPEC) 是一种对 5-HT2A 受体具有亲和力的选择性 5-HT 受体拮抗剂。Iferanserin 可用于内痔疾病的研究。 -
GC15463
Iloperidone
伊潘立酮; HP 873
An atypical antipsychotic -
GC10799
Iloperidone hydrochloride
盐酸伊潘立酮; HP 873 hydrochloride
An atypical antipsychotic -
GC12885
Imipramine (hydrochloride)
盐酸丙咪嗪
A tricyclic antidepressant -
GC14093
Indatraline hydrochloride
茚达曲林盐酸盐; Lu 19-005
Indatraline hydrochloride (Lu 19-005) 是一种非选择性单胺转运蛋白抑制剂,可阻断神经递质(多巴胺、血清素和去甲肾上腺素)的再摄取,其功效与可卡因相似。 -
GC61565
Indophagolin
5-溴-N-(4-氯-3-(三氟甲基)苯基)-1-(环丙烷羰基)吲哚啉-6-磺酰胺
Indophagolin, a potent indoline-containing autophagy inhibitor with IC50 of 140 nM, antagonizes the purinergic receptor P2X4 as well as P2X1 and P2X3 with IC50s of 2.71, 2.40 and 3.49 μM, respectively, also has a strong antagonistic effect on serotonin receptor 5-HT6 with IC50 of 1.0 μM. -
GC60938
Iprindole
伊普吲哚
Iprindole具有抗抑郁的生物活性,是一种弱的去甲肾上腺素和5-HT摄取的抑制剂。 -
GC13133
Ipsapirone
依普西隆,TVX Q 7821 free base
A partial agonist of serotonin 5-HT1A receptors -
GC31014
Irindalone (Lu 21-098)
茚达酮,Lu 21-?098
Irindalone (Lu 21-098) 是一种新型血清素 5-HT2 拮抗剂。 -
GC11984
Isamoltane hemifumarate
Isamoltane hemifumarate 是 5-HT1B 受体的选择性拮抗剂,抑制 [125I]ICYP 与大鼠脑膜中 5-HT1B 识别位点的结合,IC50 为 39 nM。
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GN10186
Isocorynoxeine
异去氢钩藤碱; 7-Isocorynoxeine
An alkaloid with diverse biological activities -
GC39076
Isopteropodine
钩藤碱 E
Isopteropodine 是从 Uncaria tomentosa 分离得到的一种异育亨宾型辛吲哚生物碱,是 M1 型毒蕈碱乙酰胆碱 (muscarinic M1) 受体及 5-HT2 受体的正向调节剂。 -
GC38433
Jatrorrhizine
药根碱
An alkaloid with diverse biological activities -
GC43926
Jatrorrhizine (chloride)
盐酸药根碱
An alkaloid with diverse biological activities -
GC60957
Jatrorrhizine hydroxide
Jatrorrhizine (Neprotin, Yatrorizine), one of the active constituents of Coptis chinensis Franch, has multiple bioactivities, such as hypoglycemic, antimicrobial, and antioxidant activities. It is an inhibitor of AChE with IC50 of 872 nM and demonstrates >115-fold selectivity for AChE over BuChE.
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GC31251
JNJ-18038683
JNJ-18038683是5-羟色胺受体7(5-HT7)的拮抗剂,HEK293细胞中检测出其对大鼠和人类5-羟色胺受体7的pKi值分别为8.19,8.20。
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GC14563
Ketanserin
酮色林; R41468
A potent 5-HT2 receptor antagonist -
GC43999
Ketanserin (tartrate)
酒石酸酮色林,R41468 tartrate
A potent 5-HT2 receptor antagonist -
GC72920
Ketanserinol
R 46742
Ketanserinol (R 46742)是酮色胺的代谢物。 -
GC60965
Keto Ziprasidone
KetoZiprasidone是Ziprasidone的杂质。Ziprasidone,一种抗精神药物,是5-HT和多巴胺(dopaminereceptor)受体拮抗剂。
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GC15121
Lasmiditan
拉米地坦
An Analytical Reference Standard -
GC36428
Lasmiditan hydrochloride
An Analytical Reference Standard
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GC25563
Lasmiditan succinate
COL-144, LY573144
Lasmiditan succinate (COL-144, LY573144) is a novel, centrally acting, highly selective 5-HT(1F) receptor agonist (Ki=2.21 nM) without vasoconstrictor activity.