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HQL 79 - ≥99%(HPLC), high purity , CAS No.162641-16-9, Inhibitor of H-PGDS

  • Moligand™
  • ≥99%(HPLC)
Item Number
H288289
Grouped product items
SKUSizeAvailabilityPrice Qty
H288289-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$296.90
H288289-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$919.90

Human hematopoietic prostaglandin D synthase (H-PGDS) inhibitor

View related series
H-PGDS Inhibitor

Basic Description

SynonymsHQL-79|162641-16-9|HQL 79|4-(BENZHYDRYLOXY)-1-[3-(1H-TETRAAZOL-5-YL)PROPYL]PIPERIDINE|4-benzhydryloxy-1-[3-(2H-tetrazol-5-yl)propyl]piperidine|1-(3-(1H-tetrazol-5-yl)propyl)-4-(benzhydryloxy)piperidine|CHEMBL574003|4-(diphenylmethoxy)-1-[3-(1h-tetrazol-5-
Specifications & PurityMoligand™, ≥99%(HPLC)
Biochemical and Physiological MechanismsOrally active and specific inhibitor of human hematopoietic prostaglandin D synthase (H-PGDS) (IC50= 6μM). Antiallergic and anti-inflammatory; displays antiasthmatic activity and potent antihistaminic propertiesin vivo.
Storage TempRoom temperature
Shipped InNormal
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of H-PGDS

Associated Targets

BRD4 Tchem Bromodomain-containing protein 4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CDK2 Tchem Cyclin-dependent kinase 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HPGDS Tchem Hematopoietic prostaglandin D synthase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

FGFR3 Tclin Fibroblast growth factor receptor 3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CSNK1D Tchem Casein kinase I isoform delta 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TRIM24 Tchem Transcription intermediary factor 1-alpha 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

BRPF1 Tchem Peregrin 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AURKA Tchem Aurora kinase A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABL1 Tclin Tyrosine-protein kinase ABL1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GSK3B Tclin Glycogen synthase kinase-3 beta 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAPK1 Tchem Mitogen-activated protein kinase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 4-benzhydryloxy-1-[3-(2H-tetrazol-5-yl)propyl]piperidine
INCHI InChI=1S/C22H27N5O/c1-3-8-18(9-4-1)22(19-10-5-2-6-11-19)28-20-13-16-27(17-14-20)15-7-12-21-23-25-26-24-21/h1-6,8-11,20,22H,7,12-17H2,(H,23,24,25,26)
InChi Key TZQGXAHOROZEKN-UHFFFAOYSA-N
Canonical SMILES C1CN(CCC1OC(C2=CC=CC=C2)C3=CC=CC=C3)CCCC4=NNN=N4
Isomeric SMILES C1CN(CCC1OC(C2=CC=CC=C2)C3=CC=CC=C3)CCCC4=NNN=N4
PubChem CID 6540277
Molecular Weight 377.48

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilitySolvent:DMSO, Max Conc. mg/mL: 9.44, Max Conc. mM: 25

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