17-phenyl-omega-trinor-PGE2

Base Information

• Chemical Name: 17-phenyl-omega-trinor-PGE2
• CAS No.: 38315-43-4
• Molecular Formula: C23H30O5
• Molecular Weight: 386.488
• DSSTox Substance ID: DTXSID80274308
• Nikkaji Number: J449.333H
• Wikidata: Q27070789
• Pharos Ligand ID: 9X4F1T8MGU47
• Metabolomics Workbench ID: 2428
• ChEMBL ID: CHEMBL1879970
• Mol file: 38315-43-4.mol

Synonyms:17-Ph-trinor-PGE2;17-phenyl-omega-trinor PGE2;17-phenyltrinorprostaglandin E2

Chemical Property of 17-phenyl-omega-trinor-PGE2

Chemical Property:

• Boiling Point: 597.1±50.0 °C(Predicted)
• PKA: 4.75±0.10(Predicted)
• PSA: 94.83000
• Density: 1 +-.0.06 g/cm3(Predicted)
• LogP: 3.30360
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 11
• Exact Mass: 386.20932405
• Heavy Atom Count: 28
• Complexity: 547

Purity/Quality:

98%,99%, ^*data from raw suppliers

17-Phenyl-trinor-prostaglandin E2 ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(C(C(C1=O)CC=CCCCC(=O)O)C=CC(CCC2=CC=CC=C2)O)O
• Isomeric SMILES: C1[C@H]([C@@H]([C@H](C1=O)C/C=C\CCCC(=O)O)/C=C/[C@H](CCC2=CC=CC=C2)O)O
• Uses: 17-Phenyl-trinor-prostaglandin E2 is a synthetic analog of PGE2 and an agonist at the EP1 and EP3 receptor (1). Prostaglandin E2(PGE2) regulates neuroinflammatory responses and is upregulated in brain injury by cyclooxygenase 2 (COX-?2) and membrane-bound PGE synthase. 17-Phenyl-trinor-prostaglandin E2 can be used to investigate inflammatory signaling pathways (2).

Technology Process of 17-phenyl-omega-trinor-PGE2

There total 1 articles about 17-phenyl-omega-trinor-PGE2 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ 17-phenyl-ω-trinor prostaglandin E2 (38315-43-4)

Guidance literature:

Refernces