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
-
GC14855
ML221
An APJ receptor antagonist
-
GC14532
TC-G 1006
S1P1 Agonist III 是一种有效且具有口服活性的 S1P1 激动剂,EC50 为 18 nM; S1P3 上没有活动。
-
GC15808
TC LPA5 4
TC LPA5 4 是一种 LPA5 (GPR92) 特异性非脂质拮抗剂。 TC LPA5 4 抑制 LPA 诱导的分离的人血小板(LPA5-RH7777 细胞系)的聚集,IC50 为 800 nM。 TC LPA5 4 显示对 LPA5 超过 80 种其他筛选药物靶点的选择性。 TC LPA5 4 抑制甲状腺癌细胞的细胞增殖和迁移。
-
GC17044
LP 20 hydrochloride
ligand of the 5-HT7 receptor
-
GC17857
PU 02
A selective 5-HT3 receptor antagonist
-
GC14350
CYM 50358 hydrochloride
S1P4拮抗剂
-
GC15903
CYM 50308
ML248
A selective S1P4 receptor agonist -
GC10728
CYM 50260
CYM 50260 是一种有效且高度选择性的 1-磷酸鞘氨醇 4 受体 (S1P4-R) 激动剂,EC50 为 45 nM。
-
GC13033
SB 611812
An antagonist of UTR
-
GC16728
SB 706375
urotensin-II (UT) receptor antagonist
-
GC17149
4-CMTB
A positive allosteric modulator of FFAR2/GPR43
-
GC10023
MK 1903
An HCA2 receptor agonist
-
GC17307
CYM 9484
CYM 9484 是一种选择性和高效的神经肽 Y (NPY) Y2 受体拮抗剂,IC50 值为 19 nM。
-
GC11851
LUF 5834
A2A and A2B adenosine receptor partial agonist
-
GC18073
TUG 891
A FFAR4 agonist
-
GC10432
IT1t dihydrochloride
A CXCR4 antagonist
-
GC13741
EMPA
An OX2R receptor antagonist
-
GC13966
CS 2100
CS 2100 (Compound 10b) 是一种有效的、选择性的、口服活性的和 S1P3 保留的 S1P1 激动剂,对人 S1P1 的 EC50 为 4.0 nM。
-
GC16605
SHA 68
An NPSR antagonist
-
GC10535
S 32212 hydrochloride
An inverse agonist of 5-HT2C receptors
-
GC11516
DV 7028 hydrochloride
5-HT2A receptor antagonist
-
GC18114
BAY 60-6583
A selective adenosine A2B receptor agonist
-
GC10495
EMD 281014 hydrochloride
7-[[4-[2-(4-氟苯基)乙基]-1-哌嗪基]羰基]-1H-吲哚-3-碳腈盐酸盐
5-HT2A antagonist -
GC16807
AT 1015
Long-acting 5-HT2A antagonist
-
GC12264
YE 120
An agonist of GPR35
-
GC10246
TC-G 1004
TC-G 1004(化合物 16j)是一种具有口服活性的 A2A 腺苷受体拮抗剂,对 hA2A 和 hA1 的 Ki 值分别为 0.44 nM 和 80 nM。
-
GC17821
VU 0365114
A positive allosteric modulator of muscarinic M5 receptors
-
GC12485
Ro 67-7476
A positive allosteric modulator of mGluR1
-
GC10646
TC-C 14G
CB1 receptor inverse agonist
-
GC14863
PSB 0777 ammonium salt
adenosine A2A receptor full agonist
-
GC14809
JNJ 10397049
An oxrexin 2 receptor antagonist
-
GC15468
NGD 98-2 hydrochloride
corticotropin-releasing factor receptor 1 (CRF1) antagonist
-
GC11946
SB 297006
A selective antagonist of CCR3
-
GC13977
MS 245 oxalate
A 5-HT6 receptor antagonist
-
GC12417
KW 3902
1,3-二丙基-8-(3-正金刚烷基)黄嘌呤,KW-3902
A selective antagonist of the adenosine A1 receptor -
GC13900
GSK 9027
GSK 9027 作为一种非甾体糖皮质激素受体 (GR) 激动剂,在 2×糖皮质激素反应元件 (GRE) 报告系统上表现为部分激动剂,并实现与地塞米松相关的内在活性。
-
GC14626
MM-22
biotinylated anandamide analog acts as a probe for visualizing the accumulation and intracellular trafficking of anandamide
-
GC13274
8-Aminoadenine
Adenine receptor agonist
-
GC14430
JNJ 5207787
An antagonist of NPY receptor Y2
-
GC14468
PSB 0739
PSB 0739 是一种高亲和力、竞争性、非选择性血小板 P2Y12 受体拮抗剂,Ki 值为 24.9 nM。
-
GC17834
Teijin compound 1
Teijin compound 1 hydrochloride
A CCR2b antagonist -
GC15183
SB 328437
A CCR3 antagonist
-
GC11161
C 021 dihydrochloride
C 021 dihydrochloride 是一种有效的 CC 趋化因子受体 4 (CCR4) 拮抗剂。
-
GC15138
SB 243213 dihydrochloride
SB 243213 dihydrochloride 是一种具有口服活性、选择性和高亲和力的 5-HT2C 受体拮抗剂,对人 5-HT2C 受体的 pKi 为 9.37,pKb 为 9.8。
-
GC14519
BX 471
ZK-811752
A selective CCR1 antagonist -
GC14392
SB 242084
6-氯-2,3-二氢-5-甲基-N-[6-[(2-甲基-3-吡啶基)氧]-3-吡啶基]-1H-吲哚-1-酰胺盐酸盐
Specific antagonist of 5-HT2C -
GC15157
SC 51322
A selective EP1 antagonist
-
GC13299
BX 513 hydrochloride
Selective CCR1 antagonist
-
GC12798
SB 258719 hydrochloride
SB 258719 hydrochloride 是一种选择性 5-HT7 受体拮抗剂,对受体具有高亲和力 (pKi=7.5)。
-
GC18146
(+)-Igmesine hydrochloride
σ1 receptor ligand