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Search Results for " hematopoietic prostaglandin d synthase "
Targets Recommended: Others Prostaglandin Receptor

8

抑制剂 & 化合物

2

重组蛋白

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Cat. No. Product Name Target Signaling Pathways
T8883 Pizuglanstat

Others; Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation; Others
Pizuglanstat 是一种前列腺素 D 合酶抑制剂,对人造血前列腺素 D 合酶的IC50为 76 nM,可用于肌再生性疾病研究。
T7948 HPGDS inhibitor 2

GSK-2894631A

PGE Synthase Immunology/Inflammation
HPGDS inhibitor 2 (GSK-2894631A) 是高效的造血前列腺素 D 合成酶(H-PGDS)选择性抑制剂(IC50:9.9 nM)。
T1804 HPGDS inhibitor 1

HPGDS-inhibitor-1

PGE Synthase Immunology/Inflammation
HPGDS inhibitor 1 是口服具有活性的HPGDS 选择性抑制剂,在酶和细胞分析中的IC50值分别为 0.6 nM 和 32 nM,但对 L-PGDS、mPGES、COX-1、COX-2 、5-LOX 无抑制作用。
T24870 TFC-007

TFC007

TFC-007 is an inhibitor of hematopoietic prostaglandin D synthase.
T15503 HQL-79

Others Others
HQL-79 is a selective and orally active human hematopoietic prostaglandin D synthase (H-PGDS) inhibitor. It inhibits the synthesis of PGD2 and acts as an anti-allergic agent (Kd: 0.8 μM and IC50: 6 μM). It also shows no obvious effect on COX-1, COX-2, m-P
T38350 TAS 205

TAS 205 is an inhibitor of hematopoietic prostaglandin D synthase (H-PGDS; IC50= 55.8 nM).1It is selective for H-PGDS over lipocalin-type PGDS (L-PGDS) at 100 μM, as well as over enzyme and receptor panels at 10 μM. TAS 205 inhibits production of prostaglandin D2induced by A23187 in KU812 human and RBL-2H3 rat basophils with IC50values of 78.3 and 181.3 nM, respectively. It inhibits ovalbumin-induced nasal lavage fluid eosinophil infiltration and late-phase nasal obstruction in an ovalbumin-sens...
T61250 HPGDS inhibitor 3

HPGDS inhibitor 3 is a powerful oral compound that selectively inhibits the hematopoietic prostaglandin D synthase (H-PGDS). With an IC50 value of 9.4 nM and EC50 of 42 nM, it demonstrates high potency in peripherally restricting H-PGDS. Moreover, HPGDS inhibitor 3 exhibits excellent selectivity with no associated central nervous system toxicity. This compound also possesses favorable pharmacokinetic properties in mouse, rat, and dog models. Additionally, HPGDS inhibitor 3 displays noteworthy an...
T41267 PROTAC(H-PGDS)-7

PROTAC(H-PGDS)-7 是一种有选择性的、有效的小分子造血前列腺素 D 合酶 (H-PGDS)PROTAC 降解剂,在 KU812细胞中展现出降解活性,DC50为 17.3 pM。PROTAC(H-PGDS)-7是一种类药化合物,能有效抑制前列腺素 D2 (PGD2)的产生,抑制炎症因子重生作用。PROTAC(H-PGDS)-7是治疗 DMD 和其他H-PGDS 相关疾病的候选化合物。

化合物

Pizuglanstat
Cat.No: T8883
Synonym:
Target: Others, Prostaglandin Receptor
HPGDS inhibitor 2
Cat.No: T7948
Synonym: GSK-2894631A
Target: PGE Synthase
HPGDS inhibitor 1
Cat.No: T1804
Synonym: HPGDS-inhibitor-1
Target: PGE Synthase
TFC-007
Cat.No: T24870
Synonym: TFC007
Target:
HQL-79
Cat.No: T15503
Synonym:
Target: Others
TAS 205
Cat.No: T38350
Synonym:
Target:
HPGDS inhibitor 3
Cat.No: T61250
Synonym:
Target:
PROTAC(H-PGDS)-7
Cat.No: T41267
Synonym:
Target:
Cat. No. Product Name Species Expression System
TMPY-04077 HPGDS/PGD2 Protein, Human, Recombinant (His)

hematopoietic prostaglandin D...

Human E. coli
HPGDS/PGD2 Protein, Human, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 24.2 kDa and the accession number is O60760.
TMPJ-00690 PGDS Protein, Human, Recombinant

Glutathione-Requiring Prostaglandin D<...

Human E. coli
Hematopoietic Prostaglandin D Synthase (HPGDS) belongs to the GST superfamily and Sigma family. HPGDS contains one GST C-terminal domain and one GST N-terminal domain. HPGDS is highly expressed in adipose tissue, macrophages, and placenta, and it exists in the form of homodimer in living body. HPGDS is a cytosolic enzyme that isomerizes PGH(2). HPGDS is a bifunctional enzyme that catalyzes both the conversion of PGH2 to PGD2 and also shows low glutathione-peroxidase activity towards cumenehydrop...

重组蛋白

HPGDS/PGD2 Protein, Human, Recombinant (His)
Cat.No: TMPY-04077
Species: Human
Expression System: E. coli
PGDS Protein, Human, Recombinant
Cat.No: TMPJ-00690
Species: Human
Expression System: E. coli
TargetMol Loading
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