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Search Results for " ep1 "
Targets Recommended: Prostaglandin Receptor

46

抑制剂 & 化合物

1

天然产物

6

重组蛋白

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Cat. No. Product Name Target Signaling Pathways
T10031 EP1-antagonist-1

EP1-antanoist-1,EP1 antagonist 1

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
EP1-antagonist-1 (EP1 antagonist 1) 是 EP1 的拮抗剂,pKi 和 pIC50 分别为 7.54 和 8.5。
T5841 Travoprost

曲伏前列素,Flu-Ipr,Fluprostenol isopropyl ester,AL6221

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
Travoprost (Fluprostenol isopropyl ester) 是一种异丙基酯前药,是一种高亲和力的,选择性的 FP 前列腺素全受体激动剂。它能够降低眼压,有潜力应用于青光眼和眼高压。
T78846 EP12

Apoptosis Apoptosis
EP12是一种c-Myc抑制剂及c-MycG4稳定剂,能够诱导多发性骨髓瘤细胞的细胞凋亡(apoptosis)及DNA损伤,并通过干扰NF-κB信号通路破坏P65/P50的核转位,从而抑制多发性骨髓瘤的生长。
TP2197 Pep1-TGL

Others Others
Peptide containing the 'TGL' motif that corresponds to the C-terminus of GluR1 subunit
T74445 ZA3-Ep10

Others Others
ZA3-Ep10是一种两性离子的脂质,用于合成脂质纳米颗粒,用于体内 RNA 传递和非病毒 CRISPR/Cas 基因编辑。
T11210 EP1013

F1013

Caspase Apoptosis; Proteases/Proteasome
EP1013 is a broad-spectrum selective inhibitor of Caspase used in the study of type 1 diabetes.
T80420 TAT-NEP1-40 acetate

Apoptosis Apoptosis
TAT-NEP1-40 acetate 是促进脑卒中后轴突再生和功能恢复的候选分子。该化合物能够抵御PC12细胞的氧和葡萄糖剥夺(OGD)损伤,并促进神经突生长。它通过抑制神经元凋亡(apoptosis)作用,保护大脑免受缺血再灌注伤害,并能有效传递至大鼠的脑内。
T80419 TAT-NEP1-40 TFA

Apoptosis Apoptosis
TAT-NEP1-40 TFA 是一种能够穿透血脑屏障的多肽。它能够保护 PC12 细胞抵御缺氧和葡萄糖剥夺 (OGD) 的损害,并促进神经突的生长。此外,TAT-NEP1-40 TFA 可通过减少缺血性脑损伤中的细胞凋亡,以改善神经系统功能。该化合物在中枢神经系统损伤,包括中风后轴突再生及功能恢复的研究中具有潜在应用价值。
T76273 Pep19-2.5

Pep19-2.5为合成抗毒素肽,能阻断内毒素信号级联。通过抑制跨膜及胞质模式识别受体(PRRs)介导的脂肽(LP)与脂多糖(LPS)的信号通路,Pep19-2.5关键调控与炎症及细胞焦亡(pyroptosis)相关的信号级联。
T81517 PEP1

PEP1为具生物活性的肽类化合物。它在低浓度时能够与POPC SLB结合,在高浓度下则会引起POPC SLB的裂解。
T80418 TAT-NEP1-40

Apoptosis Apoptosis
TAT-NEP1-40是一种能够穿透血脑屏障的多肽。它能够保护PC12细胞不受缺氧和葡萄糖剥夺(OGD)所致的损伤,同时促进神经突的生长。此外,TAT-NEP1-40通过阻断缺血性脑损伤中的细胞凋亡,对缺血后的神经功能恢复具有积极作用。该化合物适用于中枢神经系统损伤,特别是中风后的轴突再生与功能恢复方面的研究。
TP2196 Pep1-AGL

Others Others
Analog of Pep1-TGL
T14148 AH 6809

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
AH 6809 是 EP 和 DP 受体的拮抗剂,对小鼠 EP2受体的 Ki 值为 350 nM,对克隆的人类 EP1EP2,EP3-III 和 DP 受体的 Ki 值分别为 1217、1150、1597 和 1415 nM。
T21976 ONO-8130

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
ONO-8130 是前列腺素 EP1 受体选择性拮抗剂,口服有活力,能够阻断 L6 脊髓中ERK 的磷酸化。它可缓解环磷酰胺致膀胱炎小鼠的膀胱疼痛,可用于研究间质性膀胱炎。
T15689 L-798106

L 798106,CM9,GW-671021,CM-9,GW671021

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
L-798106 (CM9) 是一种具有选择性和高效性的前列腺素类 EP3 受体拮抗剂 ,抑制 EP4,EP1EP2 受体,抑制动脉粥样硬化中促炎细胞因子的水平,可减弱 PGE2 诱导的咳嗽。
T11211 EP4 receptor antagonist 1

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
EP4 receptor antagonist 1 是一种有效的特异性前列腺素 EP4受体拮抗剂,对人和小鼠 EP4受体的 IC50分别为6.1 nM 和16.2 nM。 EP4 receptor antagonist 1 可用于癌症免疫治疗的研究。
T63667 ONO-8713

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
ONO-8713 是一种选择性的前列腺素E受体亚型EP1拮抗剂,可用于研究圣经系统疾病和代谢相关疾病。
T14975 CJ-42794

CJ-042794

Others Others
CJ-42794 (CJ-042794)是前列腺素受体 EP4的选择性拮抗剂, 抑制[3H]-PGE2与 EP4受体结合的平均 pKi 为8.5, 对 EP4选择性比 EP1, EP2和 EP3高200多倍。
T63349 Treprostinil diethanolamine

UT-15C

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
Treprostinil diethanolamine (UT-15C) 是EP2、DP1和IP 的有效激动剂,对EP2、DP1、IP、EP1EP4、EP3 和 FPKi 的值分别为 3.6、4.4、32.1、212、826、2505 和 4680 nM。Treprostinil diethanolamine 能够促使 cAMP 的上调,进而维持血管系统内的稳态,并造成人肺动脉的血管扩张。
T3306 PF-04418948

PF 04418948,PF04418948

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
PF-04418948 是一种可口服的,选择性的前列腺素EP2受体拮抗剂,IC50为16 nM。
T5482 TG4-155

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
TG4-155 是一种脑渗透性 EP2 拮抗剂,对 EP2 和 DP1 具有低纳摩尔的拮抗活性。它作用于 EP2 的 KB 为 2.4 nM,比对 DP1 受体的选择性高 14 倍,比对 EP1EP3、EP4 和 IP 的选择性比高 550-4750 倍。
T23330 SC 19220

Others Others
EP1 receptor antagonist
T23332 SC 51322

Others Others
SC 51322 is an EP1 prostanoid receptor antagonist.
T27466 GSK-269984B

Others Others
GSK-269984B is a novel antagonist of EP1 receptor.
T15421 GSK-269984A

Others Others
GSK-269984A is an antagonist of Prostaglandin E2 Receptor 1 (EP1) (pIC50: 7.9).
T22125 ONO-8711

Others Others
ONO-8711 是一种有效且选择性的 EP1 受体竞争性拮抗剂(对人和小鼠 EP1 的 Ki 分别为 0.6 和 1.7 nM)。ONO-8711 在结肠癌、乳腺癌和口腔癌小鼠模型中的有效降低肿瘤发生率和多样性。
T23404 Sulprostone

Others Others
EP3 and EP1 receptor agonist
T15642 KAG-308

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
KAG-308 is an effective selective and orally active agonist of the EP4 receptor (Ki: 2.57 nM and EC50: 17 nM for human EP4 receptor), more selective over EP1, EP2, EP3, and IP receptor. KAG-308 suppresses colitis and promotes histological mucosal healing,
T16388 Omidenepag isopropyl

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
Omidenepag isopropyl is converted to the active product Omidenepag during corneal penetration. Omidenepag isopropyl is a selective EP2 receptor agonist. Omidenepag isopropyl displays only a weak affinity for EP1, EP2, and FP receptors. Omidenepag isopropy
T69229 ONO-8539

Others Others
ONO-8539 is a prostanoid EP1 receptor antagonist.
T27517 GW848687X

GW-848687X,GW 848687X

Others Others
GW848687X, a potent and selective prostaglandin EP1 receptor antagonist, is used for the treatment of inflammatory pain.
T69602 ONO-DI-004

Others Others
ONO-DI-004 is a selective EP1 Prostanoid receptor agonist.
T72513 SC 51089 free base

Others Others
SC 51089 free base 是一种选择性的前列腺素受体EP1拮抗剂,对EP1,TP,EP3和FP 受体的Ki 值分别为 1.3,11.2,17.5 和 61.1 μM。SC 51089 free base 具有神经保护活性。
T37996 17-phenyl trinor Prostaglandin E2 ethyl amide

17-phenyl trinor Prostaglandin E2 ethyl amide

Others Others
17-phenyl trinor PGE2 ethyl amide is derived from 17-phenyl trinor PGE2, a synthetic analog of PGE2 that acts as an agonist of EP1 and EP3 receptors in mice (Ki = 14 and 3.7 nM, respectively) and EP1, EP3, and EP4 in rats (Ki = 25, 4.3, and 54 nM, respectively). 17-phenyl trinor PGE2 causes contraction of guinea pig ileum at a concentration of 11 μM and is 4.4 times more potent than PGE2 as an antifertility agent in hamsters. Modification of the C-1 carboxyl group to an ethyl amide serves to inc...
T16389 Omidenepag

UR-7276

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
Omidenepag (UR-7276) 是一种具有选择性和高效性的前列腺素 E2 受体 2 (EP2)激动剂,也是一种新型局部眼部降压药。Omidenepag可用于研究青光眼和高眼压症。
T36212 16(S)-Iloprost

Others Others
Iloprost is a second generation structural analog of prostacyclin (PGI2) with about ten-fold greater potency than the first generation stable analogs, typified by carbaprostacyclin. Iloprost binds with equal affinity to the recombinant human IP and EP1 receptors with a Ki value of 11 nM. Most preparations of iloprost contain 16(S) and 16(R) stereoisomers. 16(S)-Iloprost potently inhibits platelet aggregation with an IC50 value of 3.5 nM.
T26925 Butaprost

Butaprostum,TR-4979,(R)-Butaprost

Others Others
Butaprost is a chemical compound that functions as a selective agonist for the prostaglandin E receptor (EP2). It exhibits an EC50 of 33 nM and a Ki of 2.4 μM when interacting with the murine EP2 receptor. However, Butaprost demonstrates lower activity against murine EP1, EP3, and EP4 receptors. Furthermore, it effectively attenuates fibrosis by inhibiting the TGF-β/Smad2 signaling pathway [1] [2] [3].
T37778 19(R)-hydroxy Prostaglandin E1

19(R)-hydroxy Prostaglandin E1

Others Others
19(R)-hydroxy Prostaglandin E1EP1EP3 受体亚型的激动剂,并对平滑肌表现出收缩活性,也是灵长类动物精液中的主要前列腺素。
T36080 Rivenprost

ONO-4819

Others Others
Prostaglandin E2 activates four distinct G protein-coupled receptors, EP1-4. Rivenprost is a potent and selective agonist for the EP4 receptor (Ki = 0.7, 56, 620, and >10,000 nM for EP4, EP3, EP2, and EP1, respectively). It has been used to promote EP4-mediated bone formation, prevent bone loss related to osteoporosis, drive osteoblast differentiation, and stabilize bone implants.[1][2][3][4][5] Rivenprost has also been used to support wound healing.[6]
T21869 BW A868C

Others Others
BW A868C 是一种乙内酰脲化合物,是 BW245C 结构类似物。BW A868C 是一种选择性强的前列腺素 D2 (PGD2) 竞争性拮抗剂。BW A868C 对其他前列腺素受体 (IP、EP1EP2、TP 和 FP) 没有影响。
T29907 Alprostadil sodium

PGE1 sodium salt,Prostaglandin E1 sodium

Others Others
Alprostadil sodium 是一种前列腺素受体配体,对小鼠 EP1EP2、EP3、EP4和 IP 的 Ki 值分别为 36、10、1.1、2.1 和 33 nM。它诱导血管舒张并抑制血小板聚集,可作为血管扩张剂用于外周血管疾病的研究。
T38171 Ro 1138452 hydrochloride

Others Others
Selective prostacyclin IP receptor antagonist (pKi = 8.3). Exhibits no affinity at other prostanoid receptors (EP1-4, FP and TP) in a radioligand binding assay. Demonstrates analgesic activity in rats. Orally bioavailable. Clark et al (2004) Discovery and SAR development of 2-(phenylamino) imidazolines as prostacyclin receptor antagonists. Bioorg.Med.Chem.Lett. 14 1053 PMID:15013022 |Jones et al (2006) Investigation of the prostacyclin (IP) receptor antagonist RO1138452 on isolated blood vessel ...
T84590 17-phenyl trinor Prostaglandin E2

17-phenyl trinor PGE2

Others Others
17-Phenyl trinor Prostaglandin E2 (17-phenyl trinor PGE2) is a synthetic analog of PGE2, functioning as an agonist at the EP1 and EP3 receptors. It induces contraction of the guinea pig ileum at a 11 µM concentration and displays slightly less potency than PGE2 in stimulating the gerbil colon and rat uterus. Notably, with an ED50 value of 350 µg/kg, 17-phenyl trinor PGE2 exhibits 4.4 times greater antifertility efficacy in hamsters compared to PGE2.
T36211 16(R)-Iloprost

Others Others
Iloprost is a second generation structural analog of prostacyclin (PGI2) with about ten-fold greater potency than the first generation stable analogs, typified by carbaprostacyclin. Iloprost binds with equal affinity to the recombinant human IP and EP1 receptors with a Ki value of 11 nM. Most preparations of iloprost contain 16(S) and 16(R) stereoisomers. 16(R)-Iloprost inhibits platelet aggregation with an IC50 value of 65 nM.
T23331 SC 51089

SC 51089 free base

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
SC 51089 是一种选择性的前列腺素受体 PGE2 拮抗剂,对前列腺素受体亚型具有选择性,具有抗伤害活性,可改善亨廷顿病 R6/1 小鼠模型中的运动缺陷并挽救记忆力下降。
T84587 15(R)-Prostaglandin E2

15-epi PGE2

Others Others
15(R)-Prostaglandin E2, the C-15 epimer of the more physiologically abundant 15(S)-PGE2 (sc-201225) isomer, is produced mainly from arachidonic acid (sc-200770) via the action of COX and PGES enzymes. Present in nearly all cell types, PGE2 interacts with four distinct receptors, EP1 to EP4, leading to a wide range of biological effects. However, 15(R)-Prostaglandin E2 exhibits significantly lower efficacy in most biological assays compared to its 15(S) counterpart. Notably, acid catalyzed epimer...

化合物

EP1-antagonist-1
Cat.No: T10031
Synonym: EP1-antanoist-1,EP1 antagonist 1
Target: Prostaglandin Receptor
Travoprost
Cat.No: T5841
Synonym: 曲伏前列素,Flu-Ipr,Fluprostenol isopropyl ester,AL6221
Target: Prostaglandin Receptor
EP12
Cat.No: T78846
Synonym:
Target: Apoptosis
Pep1-TGL
Cat.No: TP2197
Synonym:
Target: Others
ZA3-Ep10
Cat.No: T74445
Synonym:
Target: Others
EP1013
Cat.No: T11210
Synonym: F1013
Target: Caspase
TAT-NEP1-40 acetate
Cat.No: T80420
Synonym:
Target: Apoptosis
TAT-NEP1-40 TFA
Cat.No: T80419
Synonym:
Target: Apoptosis
Pep19-2.5
Cat.No: T76273
Synonym:
Target:
PEP1
Cat.No: T81517
Synonym:
Target:
TAT-NEP1-40
Cat.No: T80418
Synonym:
Target: Apoptosis
Pep1-AGL
Cat.No: TP2196
Synonym:
Target: Others
AH 6809
Cat.No: T14148
Synonym:
Target: Prostaglandin Receptor
ONO-8130
Cat.No: T21976
Synonym:
Target: Prostaglandin Receptor
L-798106
Cat.No: T15689
Synonym: L 798106,CM9,GW-671021,CM-9,GW671021
Target: Prostaglandin Receptor
EP4 receptor antagonist 1
Cat.No: T11211
Synonym:
Target: Prostaglandin Receptor
ONO-8713
Cat.No: T63667
Synonym:
Target: Prostaglandin Receptor
CJ-42794
Cat.No: T14975
Synonym: CJ-042794
Target: Others
Treprostinil diethanolamine
Cat.No: T63349
Synonym: UT-15C
Target: Prostaglandin Receptor
PF-04418948
Cat.No: T3306
Synonym: PF 04418948,PF04418948
Target: Prostaglandin Receptor
TG4-155
Cat.No: T5482
Synonym:
Target: Prostaglandin Receptor
SC 19220
Cat.No: T23330
Synonym:
Target: Others
SC 51322
Cat.No: T23332
Synonym:
Target: Others
GSK-269984B
Cat.No: T27466
Synonym:
Target: Others
GSK-269984A
Cat.No: T15421
Synonym:
Target: Others
ONO-8711
Cat.No: T22125
Synonym:
Target: Others
Sulprostone
Cat.No: T23404
Synonym:
Target: Others
KAG-308
Cat.No: T15642
Synonym:
Target: Prostaglandin Receptor
Omidenepag isopropyl
Cat.No: T16388
Synonym:
Target: Prostaglandin Receptor
ONO-8539
Cat.No: T69229
Synonym:
Target: Others
GW848687X
Cat.No: T27517
Synonym: GW-848687X,GW 848687X
Target: Others
ONO-DI-004
Cat.No: T69602
Synonym:
Target: Others
SC 51089 free base
Cat.No: T72513
Synonym:
Target: Others
17-phenyl trinor Prostaglandin E2 ethyl amide
Cat.No: T37996
Synonym: 17-phenyl trinor Prostaglandin E2 ethyl amide
Target: Others
Omidenepag
Cat.No: T16389
Synonym: UR-7276
Target: Prostaglandin Receptor
16(S)-Iloprost
Cat.No: T36212
Synonym:
Target: Others
Butaprost
Cat.No: T26925
Synonym: Butaprostum,TR-4979,(R)-Butaprost
Target: Others
19(R)-hydroxy Prostaglandin E1
Cat.No: T37778
Synonym: 19(R)-hydroxy Prostaglandin E1
Target: Others
Rivenprost
Cat.No: T36080
Synonym: ONO-4819
Target: Others
BW A868C
Cat.No: T21869
Synonym:
Target: Others
Alprostadil sodium
Cat.No: T29907
Synonym: PGE1 sodium salt,Prostaglandin E1 sodium
Target: Others
Ro 1138452 hydrochloride
Cat.No: T38171
Synonym:
Target: Others
17-phenyl trinor Prostaglandin E2
Cat.No: T84590
Synonym: 17-phenyl trinor PGE2
Target: Others
16(R)-Iloprost
Cat.No: T36211
Synonym:
Target: Others
SC 51089
Cat.No: T23331
Synonym: SC 51089 free base
Target: Prostaglandin Receptor
15(R)-Prostaglandin E2
Cat.No: T84587
Synonym: 15-epi PGE2
Target: Others
Cat. No. Product Name Target Signaling Pathways
T1626 Prostaglandin E1

前列地尔,PGE1,列腺素E1,Alprostadil

Endogenous Metabolite; Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation; Metabolism
Prostaglandin E1 (Alprostadil) 是一种前列腺素受体配体,对小鼠 EP1EP2、EP3、EP4和 IP 的 Ki 值分别为 36、10、1.1、2.1 和 33 nM。它诱导血管舒张并抑制血小板聚集,可作为血管扩张剂用于外周血管疾病的研究。

天然产物

Prostaglandin E1
Cat.No: T1626
Synonym: 前列地尔,PGE1,列腺素E1,Alprostadil
Target: Endogenous Metabolite, Prostaglandin Receptor
Cat. No. Product Name Species Expression System
TMPY-03329 DPEP1 Protein, Human, Recombinant (His)

MBD1,dipeptidase 1,MDP,RDP

Human HEK293 Cells
Dehydropeptidase-I, also known as DPEP1, is a kidney membrane enzyme. Its expression in normal colonic mucosa is very low, but it is highly expressed in colorectal adenoma and cancer specimens and is negatively correlated with parameters of pathological aggressiveness and poor prognosis. The overexpression of DPEP1 suppressed tumor cells invasiveness and increased sensitivity to chemotherapeutic agent Gemcitabine. Growth factor EGF treatment decreased DPEP1 expression. Dehydropeptidase-I m...
TMPH-02158 SVEP1 Protein, Human, Recombinant (hFc)

Selectin-like osteoblast-derived protein,SVEP1<...

Human HEK293 Cells
May play a role in the cell attachment process.
TMPY-01737 Meprin alpha/MEP1A Protein, Human, Recombinant (His)

meprin A, α (PABA peptide hydrolase),m...

Human HEK293 Cells
Meprin alpha/MEP1A Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 67.7 kDa and the accession number is Q16819.
TMPY-01318 Meprin alpha/MEP1A Protein, Mouse, Recombinant (His)

meprin A, alpha (PABA peptide hydrolase),A...

Mouse HEK293 Cells
Meprin alpha/MEP1A Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 69 kDa and the accession number is A0A0R4J043.
TMPJ-01351 XPNPEP1 Protein, Human, Recombinant (His)

Xaa-Pro Aminopeptidase 1,X-Prolyl Aminop

Human E. coli
X-Prolyl Aminopeptidase (XPNPEP1) is a proline-specific metalloaminopeptidase that specifically catalyzes the removal of any unsubstituted N-terminal amino acid that is adjacent to a penultimate proline residue. Because of its specificity toward proline, it has been suggested that X-Prolyl Aminopeptidase is important in the maturation and degradation of peptide hormones, neuropeptides, and tachykinins, as well as in the digestion of otherwise resistant dietary protein fragments, thereby compleme...
TMPH-02185 TEP1 Protein, Human, Recombinant (His)

p80 telomerase homolog,TEP1,Telomerase pro...

Human E. coli
Component of the telomerase ribonucleoprotein complex that is essential for the replication of chromosome termini. Also component of the ribonucleoprotein vaults particle, a multi-subunit structure involved in nucleo-cytoplasmic transport. Responsible for the localizing and stabilizing vault RNA (vRNA) association in the vault ribonucleoprotein particle. Binds to TERC. TEP1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weigh...

重组蛋白

DPEP1 Protein, Human, Recombinant (His)
Cat.No: TMPY-03329
Species: Human
Expression System: HEK293 Cells
SVEP1 Protein, Human, Recombinant (hFc)
Cat.No: TMPH-02158
Species: Human
Expression System: HEK293 Cells
Meprin alpha/MEP1A Protein, Human, Recombinant (His)
Cat.No: TMPY-01737
Species: Human
Expression System: HEK293 Cells
Meprin alpha/MEP1A Protein, Mouse, Recombinant (His)
Cat.No: TMPY-01318
Species: Mouse
Expression System: HEK293 Cells
XPNPEP1 Protein, Human, Recombinant (His)
Cat.No: TMPJ-01351
Species: Human
Expression System: E. coli
TEP1 Protein, Human, Recombinant (His)
Cat.No: TMPH-02185
Species: Human
Expression System: E. coli
TargetMol Loading
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