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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GC17929
PG-9 maleate
Increases release of acetylcholine
-
GC17723
4-IBP
NSC 667672
A σ1 receptor ligand -
GC14690
2-Iodomelatonin
2-碘褪黑激素
A potent MT1 receptor agonist -
GC14959
2-[1-(4-Piperonyl)piperazinyl]benzothiazole
5-HT4 receptor
-
GC16861
RS 23597-190 hydrochloride
3-(哌啶-1-基)丙基4-氨基-5-氯-2-甲氧基苯甲酸酯盐酸盐
RS 23597-190 hydrochloride是一种高效且有选择性的5-羟色胺4型(5-HT₄)受体(5-HT4R)拮抗剂。 -
GC11288
2-Phenylmelatonin
2-Phenylmelatonin
A MT receptor mixed partial agonist and antagonist -
GC15569
3-AQC
5-HT3 antagonist
-
GC16412
2-MPMDQ
α1-adrenoceptor antagonist,potent and selective
-
GC13338
Spiroxatrine
三氮螺癸苯恶烷
5-HT1A拮抗剂和α2C肾上腺素能受体拮抗剂 -
GC13695
2-PMDQ
α1-adrenoceptor antagonist
-
GC13357
4-PPBP maleate
4-PPBP maleate 是一种有效的 σ 1 受体配体和激动剂。
-
GC10357
Metergoline
甲麦角林
A serotonin receptor antagonist -
GC14960
PRE-084 hydrochloride
1-苯基环己烷羧酸2-(4-吗啉基)乙基酯盐酸盐
An Analytical Reference Standard -
GC10073
3-MPPI
ligand for adrenergic α1 receptor
-
GC10527
PCA 4248
PAF antagonist
-
GC11577
α-Methyl-5-hydroxytryptamine maleate
α-Me-5-HT, α-Methyl-5-HT, α-Methyl-5-hydroxytryptamine, α-Methylserotonin
A 5-HT receptor agonist -
GC15235
NAN-190 hydrobromide
A 5-HT1A receptor mixed antagonist and partial agonist
-
GC14724
Methylergometrine maleate
马来酸甲麦角新碱; Methylergonovine maleate; Ryegonovin; Spametrin F
5-HT1/5-HT2 receptor antagonist -
GC17155
MR 16728 hydrochloride
stimulates the release of acetylcholine from synaptosomes
-
GC12206
HEAT hydrochloride
HETA-盐酸盐,BE2254 hydrochloride
HEAT (BE2254) hydrochloride 是一种选择性 alpha 1 adrenergic receptor 拮抗剂。 -
GC16040
4F 4PP oxalate
A 5-HT2A receptor antagonist
-
GC16595
BD 1008 dihydrobromide
An Analytical Reference Standard
-
GC10600
1,3-Dipropyl-8-phenylxanthine
A1 adenosine antagonist
-
GC16135
Cinanserin hydrochloride
SQ 10643
A 5-HT receptor antagonist -
GC14814
5-Carboxamidotryptamine maleate
5-CT maleate
5-HT1 agonist -
GC12014
6-Chloromelatonin
6-羟基褪黑素
6-Chloromelatonin 是一种有效的褪黑激素受体激动剂,具有比褪黑激素更高的代谢稳定性。
-
GC12626
Cimaterol
西马特罗; CL 263780
A β-adrenergic agonist -
GC12463
(S)-(-)-Atenolol
(S)-(-)-阿替洛尔
(S)-(-)-Atenolol是一种强效的β-肾上腺素能受体阻滞剂。(S)-(-)-Atenolol是Atenolol的S(-)对映体,Atenolol的R(+)对映体几乎不具有β受体阻滞剂活性。 -
GC13047
N-Acetyltryptamine
N-乙酰基色胺,N10-Acetyltryptamine; Nb-Acetyltryptamine; Nω-Acetyltryptamine
A melatonin analog -
GC16349
(S)-MCPG
(+)-MCPG
An mGluR antagonist -
GC12279
(RS)-MCPG
alpha-MCPG
(RS)-MCPG (alpha-MCPG) 是一种竞争性和选择性的 I 组/II 组代谢型谷氨酸受体 (mGluR) 拮抗剂。 -
GC12394
(±)-trans-ACPD
Trans-(±)-ACP
An mGluR agonist -
GC10124
DMNPE-caged ATP diammonium salt
DMNPE-caged ATP
-
GC13360
CTCE 9908
CTCE 9908 是一种有效的选择性 CXCR4 拮抗剂。 CTCE 9908 在表达 CXCR4 的卵巢癌细胞中诱导有丝分裂灾难、细胞毒性并抑制迁移。
-
GC11818
OXA (17-33)
OXA (17-33) 是一种有效的选择性 orexin-1 受体 (OX1) 激动剂。
-
GC17626
PG 931
PG 931 是 SHU 9119 的类似物,是一种有效的黑皮质素 4 (MC4) 受体 (IC50\u003d0.58 nM) 激动剂,比对 hMC3R (IC50\u003d55 nM) 或 hMC5R (IC50\u003d2.4 nM) 更具选择性。
-
GC15030
ANQ 11125
ANQ 11125 是一种有效的选择性胃动素拮抗剂,pKd 为 8.24。
-
GC12163
PG 106
PG 106 是一种有效的选择性人黑皮质素 3 (hMC3) 受体拮抗剂 (IC50\u003d210 nM),对 hMC4 受体 (EC50\u003d9900 nM) 和 hMC5 受体没有活性。
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GC10790
FSLLRY-NH2
Selective antagonist of PAR2
-
GC14112
RFRP 3 (human)
Neuropeptide VF(124-131)(human)
RFRP-3 (Neuropeptide VF(124-131))(human) 是一种人类 GnIH 肽同源物,是一种通过抑制 Ca2+ 动员来有效抑制促性腺激素分泌的抑制剂。 -
GC10328
TT 232
CAP-232; TLN-232
A synthetic peptide derivative of somatostatin -
GC17409
PBP 10
甲酰肽受体2(FPR2)拮抗剂多肽
A peptide FPR2 antagonist -
GC16896
Grifolic acid
灰叶酸
A selective partial agonist for GPR120 -
GC11427
26RFa
孤儿受体 GPR103 的天然配体
-
GC13588
5-OMe-UDP trisodium salt
Potent P2Y6 agonist
-
GC10865
TC-MCH 7c
TC-MCH 7c 是一种苯基吡啶酮衍生物,是一种口服的、选择性的、可穿透脑的 MCH1R 拮抗剂,对 hMCH1R 的 IC50 为 5.6 nM。
-
GC13817
MRS 2957 triethylammonium salt
P2Y6 agonist
-
GC15766
Kisspeptin 10 (rat)
KiSS1 (110-119)-NH2, KiSS1 decapeptide, Kp-10, Metastin, YNWNSFGLRY-NH2
A neuropeptide and kisspeptin receptor ligand -
GC12584
MRE 3008F20
MRE 3008F20 是一种高效、高选择性的放射性腺苷 A3 受体 (AA3R) 拮抗剂 (Ki\u003d1.8 nM)。
-
GC15188
MEN 11270
B2 bradykinin receptor antagonist