20 Results for "

HPGDS

" in MedChemExpress (MCE) Product Catalog:
Products (20)

20 Results for "HPGDS" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-12791
CAS No.: 1234708-04-3
Purity:  99.92%
hPGDS-IN-1 (Compound 2 ) is an hPGDS inhibitor with an IC50 of 12 nM (as measured by fluorescence polarization assay or EIA). hPGDS-IN-1 can be used in the research of allergic rhinitis and spinal cord neurons .
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Cat. No.: HY-10439
CAS No.: 1033836-12-2
Purity:  99.42%
Target:  

PGE synthase

Research Areas:  

Inflammation/Immunology

HPGDS inhibitor 1 is a potent, selective and orally active Hematopoietic Prostaglandin D Synthase (HPGDS) inhibitor with an IC50s of 0.6 nM and 32 nM in enzyme and cellular assays, respectively. HPGDS inhibitor 1 does not inhibit human L-PGDS, mPGES, COX-1, COX-2, or 5-LOX .
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Cat. No.: HY-108259
CAS No.: 162641-16-9
Purity:  99.89%
Target:  

PGE synthase

Research Areas:  

Inflammation/Immunology

HQL-79, a potent, selective and orally active human hematopoietic prostaglandin D synthase (H-PGDS) inhibitor, highly selectively inhibits the synthesis of PGD2, and acts as an anti-allergic agent, with a Kd of 0.8 μM and an IC50 of 6 μM. Shows no obvious effect on COX-1, COX-2, m-PGES, or L-PGDS .
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Cat. No.: HY-126134
CAS No.: 2101626-26-8
Purity:  99.72%
Target:  

PGE synthase

Research Areas:  

Inflammation/Immunology

HPGDS inhibitor 2 is a highly potent and selective hematopoietic prostaglandin D synthase (H-PGDS) inhibitor with an IC50 of 9.9 nM .
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Cat. No.: HY-139972
CAS No.: 2761281-50-7
Purity:  99.42%
PROTAC(H-PGDS)-7 is a Hematopoietic prostaglandin D synthase (H-PGDS) molecular glue degrader, with a DC50 of 17.3 pM .
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Cat. No.: HY-146662
CAS No.: 2255311-93-2
Target:  

PGE synthase

Research Areas:  

Inflammation/Immunology

HPGDS inhibitor 3 is an orally active and highly potent peripherally restricted hematopoietic prostaglandin D synthase (H-PGDS) inhibitor with IC50 value of 9.4 nM and EC50 of 42 nM, respectively. HPGDS inhibitor 3 exhibits good selectivity, good pharmacokinetic parameters in mouse, rat, and dog, and no CNS toxicity. HPGDS inhibitor 3 has anti-inflammatory activity .
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Cat. No.: HY-120581
CAS No.: 1537192-31-6
Target:  

PGE synthase

Research Areas:  

Cancer

ML388 is a potent and selective hydroxyprostaglandin dehydrogenase (HPGD) inhibitor with an IC50 of 34 nM. ML388 induces PGE2 production in A549 cells and LNCaP prostate cancer cells .
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Cat. No.: HY-RS17229
Research Areas:  

Others

Hpgds Mouse Pre-designed siRNA Set A contains three designed siRNAs for Hpgds gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-110167
CAS No.: 927878-49-7
Purity:  98.01%
TFC-007, a selective hematopoietic prostaglandin D synthase (H-PGDS) inhibitor, show high inhibitory activity against H-PGDS enzyme (IC50 value of 83 nM). TFC-007 can be used for composing H-PGDS degradation inducer PROTAC(H-PGDS)-1 (TFC-007 binds to H-PGDS, and Pomalidomide binds to cereblon) .
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Cat. No.: HY-139171
CAS No.: 2250261-59-5
Purity:  99.79%
Target:  

PGE synthase

Research Areas:  

Inflammation/Immunology

F092 is an inhibitor of hematopoietic prostaglandin D synthase (H-PGDS) with a KD value of 0.14 nM. F092 can be used in the study of allergic and inflammatory responses .
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Cat. No.: HY-RS06341
Research Areas:  

Others

HPGDS Human Pre-designed siRNA Set A contains three designed siRNAs for HPGDS gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-10439R
CAS No.: 1033836-12-2
Research Areas:  

Inflammation/Immunology

HPGDS inhibitor 1 (Standard) is the analytical standard of HPGDS inhibitor 1 (HY-10439). This product is intended for research and analytical applications. HPGDS inhibitor 1 is a potent, selective and orally active Hematopoietic Prostaglandin D Synthase (HPGDS) inhibitor with an IC50s of 0.6 nM and 32 nM in enzyme and cellular assays, respectively. HPGDS inhibitor 1 does not inhibit human L-PGDS, mPGES, COX-1, COX-2, or 5-LOX .
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Cat. No.: HY-157577
CAS No.: 2761281-51-8
Research Areas:  

Neurological Disease

PROTAC (H-PGDS)-8 is an H-PGDS PROTAC inhibitor with a IC50 of 0.14 μM. PROTAC (H-PGDS)-8 binds to H-PGDS and inhibits its enzymatic activity. PROTAC (H-PGDS)-8 inhibits the production of PGD2 in cancer cells. PROTAC (H-PGDS)-8 can be used for the research of Duchenne muscular dystrophy .
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Cat. No.: HY-RS06338
Research Areas:  

Others

HPGD Human Pre-designed siRNA Set A contains three designed siRNAs for HPGD gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS06339
Research Areas:  

Others

Hpgd Mouse Pre-designed siRNA Set A contains three designed siRNAs for Hpgd gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS06340
Research Areas:  

Others

Hpgd Rat Pre-designed siRNA Set A contains three designed siRNAs for Hpgd gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS23682
Research Areas:  

Others

Hpgds Rat Pre-designed siRNA Set A contains three designed siRNAs for Hpgds gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P71036
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: HPGDS; H-PGDS; Hematopoietic Prostaglandin D Synthase; GSTS1; GSTS; PGD2; PGDS; Glutathione S-Transferase Sigma; Glutathione-Requiring Prostaglandin D Synthase; Glutathione S-Transferase; Glutathione-Dependent PGD Synthase; Epididymis Secretory Sperm Bind
Species:  
Source:  
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Cat. No.: HY-116449
CAS No.: 135-00-2
Research Areas:  

Inflammation/Immunology

2-Benzoylthiophene is an inhibitor of human hematopoietic prostaglandin D2 synthase (H-PGDS) with an IC50 value of 11.4 μM. 2-Benzoylthiophene can be used in the research of inflammatory diseases .
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Cat. No.: HY-108259R
CAS No.: 162641-16-9
Research Areas:  

Inflammation/Immunology

HQL-79 (Standard) is the analytical standard of HQL-79 (HY-108259). This product is intended for research and analytical applications. HQL-79, a potent, selective and orally active human hematopoietic prostaglandin D synthase (H-PGDS) inhibitor, highly selectively inhibits the synthesis of PGD2, and acts as an anti-allergic agent, with a Kd of 0.8 μM and an IC50 of 6 μM. Shows no obvious effect on COX-1, COX-2, m-PGES, or L-PGDS .
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