GPCR/G protein(G 蛋白偶联受体/G 蛋白)
- Neuropeptide FF/AF Receptors(49)
- Formyl Peptide Receptors(10)
- 5-HT Receptor(482)
- Acetylcholine(28)
- Adenosine Deaminase(9)
- Adenosine Receptor(130)
- Adenosine Kinase(4)
- Adiponectin Receptor(3)
- Adrenergic Receptor(407)
- Adrenergic Transporters(5)
- Apelin Receptor(9)
- Angiotensin Receptor(111)
- Bombesin Receptors(23)
- Bradykinin Receptors(29)
- Calcitonin and Related Receptors(10)
- Cannabinoid Receptor(118)
- Calcimimetic Agent(2)
- CaSR(20)
- CCK1 Receptors(7)
- CCK2 Receptors(7)
- CCR(80)
- Chemokine Receptors(23)
- CRF1 Receptors(9)
- CRF2 Receptors(3)
- CXCR(77)
- CysLT1 receptor(1)
- Endothelin Receptor(50)
- EP1 Receptor(2)
- EP4 Receptor(2)
- ERRγ(1)
- ETA Receptors(5)
- ETB Receptors(5)
- Free Fatty Acid Receptors(16)
- Galanin Receptors(11)
- Ghrelin Receptors(11)
- GHSR(19)
- GIP Receptor(5)
- Glucagon Receptor(58)
- Glucocorticoid Receptor(96)
- GLUT1(1)
- Gonadotropin-Releasing Hormone Receptors(3)
- GPCR19(12)
- GPR109A(4)
- GPR119(10)
- GPR120(9)
- GPR35(10)
- GPR55(10)
- Hydroxycarboxylic Acid Receptors(5)
- Leukotriene Receptor(55)
- LPA Receptor(12)
- LPL Receptor(59)
- LTD4 Receptor(1)
- mGluR (119)
- Melanin-concentrating Hormone Receptors(7)
- Melanocortin (MC) Receptors(54)
- Melatonin Receptors(23)
- Motilin Receptor(7)
- MT Receptor(1)
- Non-selective CRF(7)
- Neurotensin Receptors(23)
- NK2 Receptors(7)
- NK3 Receptor(5)
- NOP Receptor(19)
- NPY Receptors(26)
- Orexin(3)
- Orphan 7-TM Receptors(6)
- OX Receptor(47)
- Oxytocin Receptors(22)
- P2Y Receptor(60)
- PACAP Receptors(3)
- PAF Receptors(7)
- Peptide Receptors(14)
- PGD2 Receptor(1)
- Prostaglandin Receptor(170)
- Protease-Activated Receptors(9)
- RGS(2)
- S1P receptor(8)
- Secretin Receptors(1)
- Sensory Neuron-Specific Receptors(1)
- Somatostatin Receptor(39)
- Sigma Receptor(58)
- Vasopressin Receptor(33)
- 17,20-lyase(4)
- Ras(138)
- Urotensin-II Receptor(10)
- VIP Receptors(6)
- EBI2/GPR183(7)
- TSH Receptor(10)
- NK Receptor(1)
- GPR81(1)
- C3aR(1)
- CysLT2 receptor(1)
- S1P receptor inhibitor(22)
- CCKB(1)
- FFAR1 (GPR40)(20)
- GPR84(8)
- Neuromedin U Receptors(2)
- Kisspeptin Receptor(5)
- CRFR(25)
- RGS Protein(5)
- Urotensin Receptor(6)
- Cholecystokinin Receptor(25)
- GPR139(4)
- mAChR(183)
- MCHR1 (GPR24)(16)
- Neurokinin Receptor(75)
- Neuropeptide S Receptor(1)
- GPBA Receptor(1)
- Trace Amine 1 Receptor(2)
- GPCR protein(1)
- FFAR3(1)
- cGMP(26)
- GRK(1)
- GCGR(2)
- GLP Receptor(2)
- PTHR(1)
- Protease Activated Receptor (PAR)(2)
- Free Fatty Acid Receptor(1)
- Formyl Peptide Receptor (FPR)(1)
- Cat.No. 产品名称 Information
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GC62783
2-Methylthio-AMP diTEA
2-MeSAMP diTEA; 2-Methylthioadenosine 5′-monophosphate diTEA; 2-Methylthioadenosine 5′-phosphate diTEA
2-Methylthio-AMP (2-MeSAMP) diTEA 是一种选择性和直接的 P2Y12 拮抗剂。2-Methylthio-AMP diTEA 是 ADP 依赖性血小板聚集的抑制剂。 -
GC60016
2-Methylthioadenosine diphosphate trisodium
2-甲基硫代二磷酸腺苷,2-Methylthio-ADP trisodium
An agonist of P2Y receptors -
GC16412
2-MPMDQ
α1-adrenoceptor antagonist,potent and selective
-
GC40406
2-Oleoyl Glycerol
2-十八烯酸单甘油酯;2-甘油单油酸酯
A natural monoacylglycerol -
GC16196
2-Palmitoylglycerol
2-(1,3-二羟基丙-2-基)十六酸复合物1,3-二羟基丙-2-基棕榈酸酯(1:1),2-Palm-Gl
An endogenous fatty acid ester -
GC11288
2-Phenylmelatonin
2-Phenylmelatonin
A MT receptor mixed partial agonist and antagonist -
GC13695
2-PMDQ
α1-adrenoceptor antagonist
-
GC14753
2-ThioUTP tetrasodium salt
P2Y2 agonist
-
GC60467
21-Acetoxypregna-1,4,9(11),16-tetraene-3,20-dione
21-羟基孕甾-1,4,9(11),16-四烯-3,20-二酮-21-醋酸酯
21-Acetoxypregna-1,4,9(11),16-tetraene-3,20-dione是delta9,11类固醇类合成的中间体(intermediate),如Vamorolone 。delta9,11steroids是糖皮质激素的修饰后的产物,具有抗炎(anti-inflammatory)特性。delta9,11类固醇类可以用作保护细胞损伤(脂质过氧化)和抑制新生血管的试剂。 -
GC63737
21-Desacetyldeflazacort-D5
-
GC11427
26RFa
孤儿受体 GPR103 的天然配体
-
GC15232
3,5-DHBA
3,5-二羟基苯甲酸
hydroxycarboxylic acid receptor 1 (HCA1) agonist -
GC15569
3-AQC
5-HT3 antagonist
-
GC16689
3-chloro-5-hydroxy BA
3-氯-5-羟基苯甲酸,3-chloro-5-hydroxy BA,CHBA,GPR81 Agonist
An agonist of GPR81 -
GC60499
3-Hydroxy agomelatine
阿戈美拉汀杂质
3-Hydroxyagomelatine是Agomelatine的代谢产物。3-Hydroxyagomelatine是5-HT2C受体拮抗剂,IC50为3.2μM,Ki为1.8μM。 -
GC68328
3-Hydroxy agomelatine-d3
3-Hydroxy agomelatine D3 是 3-Hydroxy agomelatine 的氘代物。3-Hydroxy agomelatine 是 5-HT2C 受体拮抗剂,IC50 为 3.2 μM,Ki 为 1.8 μM。
-
GN10169
3-Hydroxy-4-methoxycinnamic acid
3-羟基-4-甲氧基肉桂酸,3-Hydroxy-4-methoxycinnamic acid
A cinnamic acid derivative -
GC10073
3-MPPI
ligand for adrenergic α1 receptor
-
GC62799
4,4-Diphenylbutylamine hydrochloride
4,4-二苯基丁胺(盐酸盐)
4,4-Diphenylbutylamine 对 5-HT2A 和 H1 受体的 Ki 值分别为 2589 和 1670 nM。 -
GC17149
4-CMTB
A positive allosteric modulator of FFAR2/GPR43
-
GC39678
4-Deoxypyridoxine 5'-phosphate
4-Deoxypyridoxine Phosphate, DOP-P, DOP Phosphate, NSC 29870
A vitamin B6 analog and an inhibitor of S1P lyase -
GC68327
4-Hydroxyatomoxetine-d3
4-Hydroxyatomoxetine D3 是 4-Hydroxyatomoxetine 的氘代物。4-Hydroxyatomoxetine 是 Atomoxetine (Tomoxetine) 的活性代谢产物。4-Hydroxyatomoxetine 通过细胞色素 P450 2D6 (CYP2D6) 酶代谢。Atomoxetine 是一种有效的选择性去甲肾上腺素再摄取抑制剂。
-
GC64116
4-Hydroxypropranolol-d7
(±)-4-Hydroxy Propranolol-d7
4-Hydroxypropranolol-d7 ((±)-4-Hydroxy Propranolol-d7) 是 4-Hydroxypropranolol hydrochloride 的氘代物。4-Hydroxypropranolol hydrochloride 是 Propranolol 的活性代谢产物。4-Hydroxypropranolol hydrochloride 的效力与 Propranolol 相当。4-Hydroxypropranolol hydrochloride 抑制 β1-和 β2-肾上腺素能受体,pA2 值分别为 8.24 和 8.26。4-Hydroxypropranolol hydrochloride 具有固有的拟交感活性,膜稳定活性和强效的抗氧化性能。 -
GC70207
4-Hydroxypropranolol-d7 hydrochloride
4-Hydroxypropranolol-d7 hydrochloride是氘标记的4-羟基普萘洛尔盐酸盐。
-
GC17723
4-IBP
NSC 667672
A σ1 receptor ligand -
GC42460
4-Nitrophenyl Phenylphosphonate
苯膦酸单-4-硝基苯酯
A 5′-nucleotide phosphodiesterase substrate -
GC16186
4-P-PDOT
AH 024
An antagonist of the MT2 receptor -
GC13357
4-PPBP maleate
4-PPBP maleate 是一种有效的 σ 1 受体配体和激动剂。
-
GC17100
4-Quinolone-3-Carboxamide CB2 Ligand
4Q3C CB2 Ligand
An Analytical Reference Standard -
GC15850
4-Quinolone-3-Carboxamide Furan CB2 Agonist
4Q3C CB2 Agonist
Selective CB2 agonist -
GC16040
4F 4PP oxalate
A 5-HT2A receptor antagonist
-
GC11002
5'-(N-Cyclopropyl)carboxamidoadenosine
CPCA
A specific adenosine A2 receptor agonist -
GC14814
5-Carboxamidotryptamine maleate
5-CT maleate
5-HT1 agonist -
GC31234
5-HT1A modulator 1
5-HT1Amodulator1对5HT1A,肾上腺素能α1和多巴胺D2受体具有非常高的亲和力,IC50分别为2±0.3nM,10±3nM和40±9nM。
-
GC60028
5-HT1A modulator 2 hydrochloride
8-甲氧基-2-四氢萘胺
5-HT1Amodulator2hydrochloride是8-OH-DPAT的一种衍生物,5-HT1Amodulator2hydrochloride是5-HT1A的调节剂,与5-HT1A结合的Ki值为53nM。 -
GC32655
5-HT2 antagonist 1
5-HT2antagonist1是一种有效的5-HT2receptor拮抗剂,同时对α1adrenoceptor有微弱地抑制作用。
-
GC32664
5-HT2A antagonist 1
5-HT2Aantagonist1是来自专利US5728835A和JP1007727的5-HT2A拮抗剂。5-HT2Aantagonist1可能用于治疗心血管疾病的研究。
-
GC71279
5-HT2A receptor agonist-3
5-HT2A receptor agonist-3Ki=2.5nM、对5-HT2A的选择性是结构相似的5-HT2C受体的124倍。
-
GC65568
5-HT2B antagonist-1
WAY-388264-A is a bioactive compound.
-
GC31263
5-HT3 antagonist 1
5-HT3antagonist1是一种有效的选择性的serotonin3(5-HT3)receptor拮抗剂。
-
GC31247
5-HT3 antagonist 2
5-HT3antagonist2是5-HT3受体的拮抗剂。
-
GC65983
5-HT3 antagonist 5
5-HT3 antagonist 5 是一种喹喔啉 -2- 甲酰胺化合物,是 5-HT3 受体拮抗剂。5-HT3 antagonist 5 对 5-HT3 激动剂和 2- 甲基 -5-HT 也具有拮抗作用,并在小鼠中表现出抗抑郁效果。
-
GC31227
5-HT3-In-1
5-HT3-In-1来自专利EP0748807A1,化合物实例8。它有抑制5-HT3的活性。
-
GC30314
5-HT4 antagonist 1
5-HT4antagonist1是一个5-HT4受体拮抗剂,其pKi值为9.6。
-
GC31144
5-HT7 agonist 1
5-HT7agonist1是一种选择性的5-HT7受体激动剂,IC50值为222.93nM,可用于研究与5-HT7受体相关的疾病,例如中枢神经系统疾病。
-
GC14801
5-Iodotubercidin
5-碘代杀结核菌素,NSC 113939; 5-ITu
An adenosine kinase inhibitor -
GC14940
5-Methoxytryptamine
5-甲氧基色胺
-
GC64182
5-Methoxytryptamine hydrochloride
5-甲氧基色胺盐酸盐
5-Methoxytryptamine hydrochloride,一种 Melatonin 的代谢物,是一种非选择性 5-HT 受体激动剂。5-Methoxytryptamine hydrochloride 对 5-HT3 受体没有亲和力。5-Methoxytryptamine hydrochloride 也是一种有效的抗氧化剂,并具有辐射防护作用。 -
GC35168
5-O-Demethylnobiletin
去甲基川陈皮素,5-Demethylnobiletin
A flavonoid with diverse biological activities -
GC13588
5-OMe-UDP trisodium salt
Potent P2Y6 agonist