PGB1 (Prostaglandin B1) - 98%, high purity , CAS No.13345-51-2

  • ≥98%
Item Number
P336176
Grouped product items
SKUSizeAvailabilityPrice Qty
P336176-1mg
1mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$23.90
P336176-5mg
5mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$106.90
P336176-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$202.90

a metabolite of PGA1 shown to modify the pressor responses to sympathetic nerve stimulation

View related series
Prostaglandin Receptor

Basic Description

SynonymsJ-006385 | BDBM50390997 | ALPROSTADIL IMPURITY B [EP IMPURITY] | SR-01000000044-6 | BML1-F03 | DTXSID001347609 | NCGC00024019-03 | PGB1 (Prostaglandin B1) | Prosta-8(12),13-dien-1-oicacid, 15-hydroxy-9-oxo-, (13E,15S)- | HY-120665 | SR-01000000044 | NCGC0
Specifications & Purity≥98%
Storage TempProtected from light,Store at -20°C
Shipped InIce chest + Ice pads
Product Description

PGB1 (Prostaglandin B1) is a nonenzymatic dehydration product of PGE1 and a metabolite of PGA1 that has been shown to modify the pressor responses to sympathetic nerve stimulation. Furthermore, when PGB1 is oligomerized it has been shown to inhibit phospholipase A|2|, and act as an ionophore for calcium.

Product Properties

pKapKₐ: 4.77

Associated Targets(Human)

VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLB Tchem DNA polymerase beta (23632 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PLK1 Tchem Serine/threonine-protein kinase PLK1 (28605 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HIF1A Tchem Hypoxia-inducible factor 1 alpha (6027 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL (112 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLK Tbio DNA polymerase kappa (8653 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLH Tchem DNA polymerase eta (21678 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RECQL Tbio ATP-dependent DNA helicase Q1 (5575 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RGS4 Tchem Regulator of G-protein signaling 4 (13867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLS Tchem Glutaminase kidney isoform, mitochondrial (16997 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
WRN Tbio Werner syndrome ATP-dependent helicase (8824 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Cruzipain (33337 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Chlamydia pneumoniae (241 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Luciferin 4-monooxygenase (66902 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Cholinesterase (8742 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slco2a1 Solute carrier organic anion transporter family member 2A1 (47 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 7-[2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopenten-1-yl]heptanoic acid
INCHI InChI=1S/C20H32O4/c1-2-3-6-9-17(21)14-12-16-13-15-19(22)18(16)10-7-4-5-8-11-20(23)24/h12,14,17,21H,2-11,13,15H2,1H3,(H,23,24)/b14-12+/t17-/m0/s1
InChi Key YBHMPNRDOVPQIN-VSOYFRJCSA-N
Canonical SMILES CCCCCC(C=CC1=C(C(=O)CC1)CCCCCCC(=O)O)O
Isomeric SMILES CCCCC[C@@H](/C=C/C1=C(C(=O)CC1)CCCCCCC(=O)O)O
WGK Germany 3
PubChem CID 5280388
Molecular Weight 336.5
Beilstein 2004447

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot NumberCertificate TypeDateItem
F2313492Certificate of AnalysisJun 06, 2023 P336176
F23131510Certificate of AnalysisJun 06, 2023 P336176
F23131546Certificate of AnalysisJun 06, 2023 P336176
F23131481Certificate of AnalysisJun 06, 2023 P336176

Chemical and Physical Properties

SolubilitySoluble in acetone (20 mg/ml), methanol (>50 mg/ml), acetonitrile (>50 mg/ml), DMSO (~50 mg/ml), PBS (7.2) (~2 mg/ml), DMF (~50 mg/ml), and ethanol (~50 mg/ml). Insoluble in water.
SensitivityLight sensitive
Refractive Indexn20D1.55
Boil Point(°C)~531.4° C at 760 mmHg (Predicted)
Melt Point(°C)69-71°C

Safety and Hazards(GHS)

WGK Germany 3

Related Documents

Citations of This Product

1. Lihui Xuan, Yin Wang, Can Qu, Yuhui Yan, Wensen Yi, Jingjing Yang, Magdalena Skonieczna, Cuimei Chen, Justyna Miszczyk, Dmitry S. Ivanov, Hesham M.H. Zakaly, Vladimir Markovic, Ruixue Huang.  (2023)  Metabolomics reveals that PS-NPs promote lung injury by regulating prostaglandin B1 through the cGAS-STING pathway.  CHEMOSPHERE,  342  (13): (140108).  [PMID:37714480] [10.1016/j.chemosphere.2023.140108]

References

1. Lihui Xuan, Yin Wang, Can Qu, Yuhui Yan, Wensen Yi, Jingjing Yang, Magdalena Skonieczna, Cuimei Chen, Justyna Miszczyk, Dmitry S. Ivanov, Hesham M.H. Zakaly, Vladimir Markovic, Ruixue Huang.  (2023)  Metabolomics reveals that PS-NPs promote lung injury by regulating prostaglandin B1 through the cGAS-STING pathway.  CHEMOSPHERE,  342  (13): (140108).  [PMID:37714480] [10.1016/j.chemosphere.2023.140108]

Solution Calculators