Histamine Receptor(组胺受体)
Histamine receptor has 4 subtypes (H1,H2,H3 and H4) which mediates various biological fuctions, including allergic reaction, gastric acid secretion and inflammation etc.
Products for Histamine Receptor
- Cat.No. 产品名称 Information
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GC39735
Triprolidine hydrochloride monohydrate
盐酸曲普利啶一水合物
Triprolidine Hydrochloride is the hydrochloride salt form of Triprolidine, which is the first generation histamine H1 antagonist used in allergic rhinitis. -
GC39479
Bepotastine
贝他斯汀
A histamine H1 receptor antagonist -
GC39378
Emedastine
依美斯汀
A histamine H1 receptor antagonist - GC50405 JNJ 39758979 dihydrochloride 高亲和力和选择性组胺H4拮抗剂;口服生物利用度
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GC46185
Nimbin
宁宾
A limonoid with diverse biological activities -
GC38558
PF-03654746 Tosylate
反式-N-乙基-3-氟-3-[3-氟-4-(1-吡咯烷基甲基)苯基]-环丁烷甲酰胺4-甲基苯磺酸盐
PF-03654746 Tosylate (PF-03654746) 是一种有效的选择性组胺 H3 receptor 拮抗剂,具有脑渗透性。PF-03654746 Tosylate (PF-03654746) 可减少过敏原引起的鼻炎反应。PF-03654746 Tosylate (PF-03654746) 用于治疗人类认知障碍,改善阿尔茨海默病人 (AD) 的认知。 - GC38450 LML134 LML134 (化合物 18b) 是一种具有口服活性,高选择性 H3R (组胺 3 受体) 反向激动剂,对 hH3R 的 cAMP 和 bdg 的 Kis 分别为 0.3 nM 和 12 nM。LML134 快速穿透大脑,导致高 H3R 占有率,并以快速的动力学特征使其目标脱离。LML134 用于治疗过度睡眠障碍。
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GC37959
Zaltidine
唑替丁,CP-57361
Zaltidine(CP-57361)是H2受体拮抗剂,有抗分泌活性。 -
GC36932
Pitolisant oxalate
PITOLISANT草酸盐,Tiprolisant oxalate
A histamine H3 receptor antagonist and inverse agonist -
GC36931
Pitolisant
替洛利生,Tiprolisant
A histamine H3 receptor antagonist and inverse agonist - GC36878 PF-03654746 PF-03654746 是一种有效的选择性 H3 histamine H3 receptor 受体拮抗剂,具有高脑渗透性。PF-03654746 可减少过敏原引起的鼻腔症状,可能是进一步探索过敏性鼻炎的新型治疗策略。PF-03654746 提高阿尔茨海默病 (AD) 的认知功效和改善疾病的效果。
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GC36875
Perphenazine D8 Dihydrochloride
奋乃静 D8 二盐酸盐
Perphenazine D8二盐酸盐是Perphenazine氘代化合物标准品。 -
GC36476
Lodoxamide tromethamine
洛度沙胺氨丁三醇,U-42585E
A potent agonist of GPR35 and a mast cell stabilizer -
GC36279
Hydroxyzine pamoate
双羟萘酸羟嗪;拉姆酸羟嗪;扑姆酸羟嗪;双羟萘酸羟嗪
Hydroxyzine Pamoate is the pamoate salt form of hydroxyzine, a synthetic piperazine histamine H1-receptor antagonist with anti-allergic, antispasmodic, sedative, anti-emetic and anti-anxiety properties. -
GC36278
Hydroxyzine D4 dihydrochloride
Vistaril-d4' dihydrochloride; Atarax-d4' dihydrochloride
Hydroxyzine D4二盐酸盐是Hydroxyzine氘代化合物标准品。 -
GC35826
Decloxizine dihydrochloride
盐酸去氯羟嗪; UCB 1402 dihydrochloride
Decloxizine(UCB-1402; NSC289116)二盐酸盐1型组胺受体H1拮抗剂。 -
GC35656
Cetirizine D8 dihydrochloride
盐酸西替利嗪 D8
An internal standard for the quantification of cetirizine,(R)-cetirizine, and (S)-cetirizine -
GC35655
Cetirizine D4 dihydrochloride
盐酸西替利嗪 D4
Cetirizine D4二盐酸盐是Cetirizine氘代化合物标准品。 -
GC35473
Bavisant dihydrochloride hydrate
JNJ31001074AAC; JNJ31001074 dihydrochloride hydrate
Bavisant dihydrochloride hydrate (JNJ31001074AAC) 是口服活性人H3 受体拮抗剂。 -
GC35472
Bavisant dihydrochloride
JNJ-31001074 dihydrochloride
Bavisant盐酸盐(JNJ-31001074)是口服活性人H3受体拮抗剂。 -
GC35471
Bavisant
JNJ-31001074
Bavisant (JNJ-31001074)是口服活性人H3受体拮抗剂。 -
GC35284
Alimemazine D6
阿利马嗪D6,Trimeprazine D6
Alimemazine D6是Alimemazine氘代化合物标准品。 - GC35222 ABT-239 ABT-239 是一种新颖的,高效的,非咪唑类的 H3R 拮抗剂,也是 TRPV1 的拮抗剂。
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GC44360
Nedocromil (sodium salt)
奈多罗米钠,FPL 59002KP; Nedocromil disodium salt
A mast cell stabilizer -
GC43598
Emedastine (fumarate)
富马酸依美斯汀;富马酸依美司丁
A histamine H1 receptor antagonist -
GC43427
Dexchlorpheniramine (maleate)
马来酸右氯苯那敏; S-(+)-Chlorpheniramine maleate salt
A histamine H1 receptor antagonist -
GC43353
Cyproheptadine (hydrochloride hydrate)
盐酸赛庚啶半水合物
An antihistamine with antiserotonergic and anticholinergic activities -
GC41715
(R)-Cetirizine (hydrochloride)
盐酸左西替利嗪,(R)-Cetirizine dihydrochloride
A selective histamine H1 receptor antagonist - GC34338 H3R-IN-1 Hydrochloride H3R-IN-1Hydrochloride是一种有效的组胺受体3(H3R)反向激动剂,详细信息请参考专利文献WO2013107336A1中的化合物2。
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GC33879
Azelastine
氮卓斯汀
Azelastine HCl is a potent, second-generation, selective, histamine receptor antagonist, used in the treatment of rhinitis. -
GC33544
(±)-Methotrimeprazine (D6) (dl-Methotrimeprazine D6)
(±)-Methotrimeprazine-d6; dl-Methotrimeprazine-d6
(±)-Levomepromazine D6 ((±)-Methotrimeprazine D6) 是氘标记的 Methotrimeprazine,它是一种 D3 多巴胺和组胺 H1 受体拮抗剂。 -
GC33499
Fexofenadine D6 (MDL-16455 D6)
非索非那定-D6,MDL-16455-d6; Terfenadine carboxylate-d6
Fexofenadine D6 (MDL-16455 D6) 被氘标记为 Fexofenadine,它是一种抗组胺药。 -
GC32979
Chloropyramine hydrochloride
盐酸氯吡胺
Chloropyramine hydrochloride (Halopyramine) is a histamine receptor H1 antagonist and has anti-cholinergic, antispasmodic, and antiallergic effects. - GC32050 FRG8701 FRG-8701是一种新组氨酸H2-receptor拮抗剂,IC50值为0.25至0.43μM。
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GC32001
KP136 (AL136)
AL136
KP136 (AL136) (AL136) 是一种口服有效的抗过敏剂。 - GC31994 CI-949 CI-949是一种过敏介质释放抑制剂,可抑制组胺(histamine),白三烯C4/D4(LTC4/LTD4)和血栓素B2(TXB2)的释放,IC50分别为11.4μM,0.5μM和0.1μM。
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GC31897
Pirolate (CP-32387)
匹罗酯,CP-32387
Pirolate (CP-32387) 是一种组胺 H1 受体拮抗剂。 -
GC31884
H4R antagonist 1
H4Rantagonist1是一种有效的高选择性组胺H4受体(H4R)拮抗剂,IC50为27nM。H4Rantagonist1对组胺受体的其他亚型H1R,H2R和H3R没有任何明显的结合亲和力。
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GC31877
BMY-25271
BMY-25271是一个组胺H2受体(histamineH2receptor)拮抗剂。
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GC31848
Mebhydrolin napadisylate (Mebhydroline 1,5-naphthalenedisulfonate salt)
美海屈林萘二磺酸盐,Mebhydroline 1,5-naphthalenedisulfonate salt
Mebhydrolin Napadisylate (Diazoline, Diazolin, Incidal, Omeril) is classified as an antihistamine drug classes used to treat allergies. -
GC31840
Bamirastine (TAK-427)
TAK-427
Bamirastine (TAK-427) 抑制配体与重组人组胺 H1 受体 (rhH1R) 的结合,IC50 值为 17.3 nM。 - GC31824 Wy 49051 Wy49051是一种有效的,可口服的H1receptor拮抗剂,IC50值为44nM。
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GC31820
Quinotolast sodium (FR71021)
FR71021
浓度范围为 1-100 μg/mL 的 Quinotolast sodium (FR71021) 以浓度依赖性方式抑制组胺、LTC4 和 PGD2 的释放。 -
GC31812
ReN-1869 hydrochloride (NNC-05-1869 hydrochloride)
NNC-05-1869 hydrochloride
ReN 1869 hydrochloride 是一种新型选择性组胺 H1 受体拮抗剂,对组胺 H1 受体(豚鼠脑)具有亲和力,Ki 为 0.19±;0.04 μ;M 和非选择性 σ;位点(豚鼠脑),Ki 为 0.45 μ;M. - GC31800 SUN 1334H SUN1334H是一种有效的,可口服的,选择性的H1receptor拮抗剂,Ki值为9.7nM。
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GC31790
PF-3893787 hydrochloride
PF-3893787 hydrochloride
PF-3893787 hydrochloride (PF-3893787 hydrochloride) 是一种新型的组胺 H4 受体拮抗剂结合亲和力 (Ki=2.4 nM),也是一种功能性 (Ki=1.56 nM) 拮抗剂。 -
GC31787
Mebhydrolin
美海屈林;美海洛林;甲苄咔啉;
Mebhydrolin是一种特异性组胺H1受体拮抗剂。 - GC31767 Peptide 401 Peptide401是一种有效的来源于蜂毒中的肥大细胞脱颗粒肽,抑制血管通透性。
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GC31750
Fenspiride Hydrochloride
Decaspiride
Fenspiride盐酸盐是肾上腺素能受体和H1受体拮抗剂。 -
GC31743
Mequitazine (LM-209)
美喹他嗪; LM-209
Mequitazine (LM-209) is a histamine H1 antagonist which competes with histamine for the normal H1-receptor sites on effector cells of the gastrointestinal tract, blood vessels and respiratory tract.