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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GC16395
Carteolol HCl
盐酸卡替洛尔; OPC-1085 hydrochloride
A β-adrenergic receptor antagonist -
GC16820
ELN441958
ELN441958 是一种有效、中性、竞争性和选择性的缓激肽 B1 受体拮抗剂,对天然人缓激肽 B1 受体的 Ki 为 0.26 nM。
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GC17249
PF-3274167
An oxytocin receptor antagonist
-
GC15319
Cyclosporin H
环孢菌素H
环孢菌素H(Cyclosporin H)是一种有效的选择性甲酰基肽受体(FPR)拮抗剂,IC50值为0.7μM。 -
GC15449
Rolapitant
罗拉匹坦; SCH619734
A potent NK1 receptor antagonist -
GC13082
Regadenoson
瑞加德松; CVT-3146
A short-acting A2A receptor agonist -
GC10005
SEP-0372814
A PDE10A inhibitor
-
GC10075
Methylprednisolone Sodium Succinate
甲基泼尼松龙琥珀酸钠
A prodrug form of methylprednisolone -
GC14266
CCG 203971
An inhibitor of the Rho/MKL1/SRF transcriptional pathway
-
GC12956
ML224
NCGC00242364; ANTAG3
ML224(NCGC00242364; ANTAG3) 是一种选择性 TSHR 反向激动剂;抑制 TSH 刺激的 cAMP 产生,IC50 = 2.3 μM。 -
GC12795
CCG-1423
An inhibitor of Rho-mediated cell signalling
-
GC17538
UNBS 5162
A antagonist of CXCL chemokine expression
-
GC14980
MK-571 sodium salt hydrate
L-660711
MK-571 钠盐水合物,作为白三烯 D4 作用的强效特异性拮抗剂,用于治疗哮喘。 -
GC14612
JNJ-31020028
An antagonist of NPY receptor Y2
-
GC11784
LCZ696
沙库必曲/缬沙坦; LCZ696
A dual angiotensin II receptor antagonist and neprilysin inhibitor -
GC17401
RG7090
Basimglurant, RO4917523
A negative allosteric modulator of mGluR5 -
GC10906
RBC8
A Ral inhibitor
-
GC13445
LY2119620
3-氨基-5-氯-N-环丙基-4-甲基-6-[2-(4-甲基-1-哌嗪基)-2-氧代乙氧基]-噻吩并[2,3-B]吡啶-2-甲酰胺
A positive allosteric modulator of M2 and M4 mAChRs -
GC12247
K-Ras(G12C) inhibitor 12
An allosteric inhibitor of oncogenic K-Ras(G12C)
-
GC10887
Labetalol HCl
盐酸拉贝洛尔; AH-5158 hydrochloride; Sch-15719W
An antagonist of α- and β-adrenoreceptors -
GC10612
BQU57
An inhibitor of RalA and RalB
-
GC15478
6H05
6H05(6H零5)
An allosteric inhibitor of oncogenic K-Ras(G12C) -
GC16465
SB 225002
SB 225002是一种有效的选择性CXCR2趋化因子受体拮抗剂,可抑制125I-IL-8(125I标记的白细胞介素8)和CXCR2的结合,IC50值为22nM。
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GC10300
Diphenidol HCl
盐酸地芬尼多; Difenidol hydrochloride
A muscarinic acetylcholine receptor antagonist -
GC12242
MK 6096
MK-6096
A dual orexin receptor antagonist -
GC16176
GSK 137647
4-甲氧基-N-(2,4,6-三甲基苯)苯磺酰胺,GSK 137647
A selective GPR120 agonist -
GC17753
AH 7614
NSC 31171,N-xanthen-9-yl-p-Toluenesulfonamide
A selective FFAR4 antagonist -
GC15716
TCS 3035
TCS 3035 (compound 10) 是一种有效的 GPR35 激动剂,pEC50 为 5.86。
-
GC11844
Pimavanserin
匹莫范色林; ACP-103
A 5-HT2A inverse agonist -
GC15430
NIBR189
A selective antagonist of EBI2 (GPR183)
-
GC17742
NF 340
NF 340 是一种有效的选择性 P2Y11 受体拮抗剂。
-
GC13458
SB 265610
A selective CXCR2 inverse agonist
-
GC14317
BMS CCR2 22
2-(3-异丙基脲基)-N-(2-((1R,2S)-2-(4-(甲基硫基)苯甲酰胺基)环己基氨基)-2-氧代乙基)-5-(三氟甲基)苯甲酰胺
BMS CCR2 22 是一种有效、特异性和高亲和力的 CC 型趋化因子受体 2 (CCR2) 拮抗剂,具有出色的结合亲和力(结合 IC50 为 5.1 nM)和有效的功能拮抗作用(钙通量 IC50 为 18 nM,趋化性 IC50 为 1 nM) 。 -
GC11797
CI 1020
endothelin-A receptor (ETA) antagonist
-
GC14554
J 113863
J 113863 是一种有效的选择性 CCR1 (CD18) 拮抗剂,对人和小鼠 CCR1 受体的 IC50 值分别为 0.9 nM 和 5.8 nM。
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GC12328
SCH 442416
2-(2-呋喃基)-7-[3-(4-甲氧苯基)丙基]-7H-吡唑并[4,3-E][1,2,4]三唑并[1,5-C]嘧啶-5-胺
An A2AR antagonist -
GC17932
L-AP4
L(+)-2-氨基-4-膦酰基丁酸,L-APB
A selective Group III metabotropic glutamate receptor agonist -
GC16336
ACT 335827
ACT 335827 是一种选择性、口服活性、脑渗透性食欲素 1 型受体拮抗剂。
-
GC17088
SA 4503 dihydrochloride
1-[2-(3,4-二甲氧基苯基)乙基]-4-(3-苯基丙基)哌嗪盐酸盐,SA4503 dihydrochloride; AGY94806 dihydrochloride
A selective σ1 receptor agonist -
GC18138
CYM 50769
An NPBWR1 antagonist
-
GC16946
CYM 5541
ML249
A selective agonist of S1P3 -
GC14478
LUF 6283
A partial agonist of GPR109A/HCA2 receptors
-
GC15721
TC-G 1001
TC-G 1001 (compound 11) 是一种有效的 GPR35 激动剂,在 β-arrestin 和 Ca2+ 释放试验中的 EC50 分别为 26 和 3.2 nM。
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GC14436
H2L5186303
A selective LPA2 receptor antagonist
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GC15428
H2L 5765834
H2L 5765834 是溶血磷脂酸受体 LPA1、LPA3 和 LPA5 的拮抗剂,IC50 分别为 94、752 和 463 nM。
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GC11067
PF 04418948
An orally active, potent, selective EP2 receptor antagonist
-
GC11338
Org 37684
Org 37684 是一种高效的 5-HT2C 受体激动剂 (pEC50\u003d8.17)。
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GC16232
BETP
A positive allosteric modulator of GLP-1R
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GC18110
COR 170
COR 170 (11u) 是一种选择性 CB2 反向激动剂,它是一种 4-喹诺酮-3-羧酸衍生物,对 CB2 受体的 Ki 值为 3.8 nM。
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GC17172
Q94 hydrochloride
A Gαq-signaling-biased PAR1 antagonist