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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 EP1,EP2,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,EP1 和 EP2 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、EP1、EP4、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 EP1、EP3、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 E1 是 EP1 和 EP3 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、EP1、EP2、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 EP1、EP2、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... |
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 EP1、EP2、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。 |
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... |