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514-39-6 molecular structure
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4-[(1S,2R,5S,7S,10R,11S,14R,15R)-5,7,11-trihydroxy-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadecan-14-yl]-2,5-dihydrofuran-2-one

ChemBase ID: 179727
Molecular Formular: C23H34O5
Molecular Mass: 390.51306
Monoisotopic Mass: 390.24062419
SMILES and InChIs

SMILES:
[C@@]12([C@@]([C@@H](C3=CC(=O)OC3)CC2)(CC[C@@H]2[C@@]3([C@@](C[C@H](CC3)O)(CC[C@@H]12)O)C)C)O
Canonical SMILES:
O[C@H]1CC[C@]2([C@](C1)(O)CC[C@@H]1[C@@H]2CC[C@]2([C@]1(O)CC[C@@H]2C1=CC(=O)OC1)C)C
InChI:
InChI=1S/C23H34O5/c1-20-7-3-15(24)12-22(20,26)9-5-18-17(20)4-8-21(2)16(6-10-23(18,21)27)14-11-19(25)28-13-14/h11,15-18,24,26-27H,3-10,12-13H2,1-2H3/t15-,16+,17-,18+,20+,21+,22-,23-/m0/s1
InChIKey:
QJPCKAJTLHDNCS-FBAXFMHRSA-N

Cite this record

CBID:179727 http://www.chembase.cn/molecule-179727.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
4-[(1S,2R,5S,7S,10R,11S,14R,15R)-5,7,11-trihydroxy-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadecan-14-yl]-2,5-dihydrofuran-2-one
IUPAC Traditional name
4-[(1S,2R,5S,7S,10R,11S,14R,15R)-5,7,11-trihydroxy-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadecan-14-yl]-2,5-dihydrofuran-2-one
Synonyms
Periplogenin
CAS Number
514-39-6
PubChem SID
164235637
PubChem CID
10574

DATA SOURCES

DATA SOURCES

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Data Source Data ID Price
InterBioScreen
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Data Source Data ID
PubChem 10574 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 7.1826363  H Acceptors
H Donor LogD (pH = 5.5) 1.826343 
LogD (pH = 7.4) 1.4129112  Log P 1.8352609 
Molar Refractivity 105.1251 cm3 Polarizability 41.84968 Å3
Polar Surface Area 86.99 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Pharmacology Properties Product Information Bioassay(PubChem)
Mechanism of Action
Apoptosis inductor expand Show data source
Biological Source
Aglycone from Alloemicymarin, also in seeds of Speirantha preussii expand Show data source
Application(s)
Antiproliferative activity toward three human-derived (HT-1080 fibrosarcoma, lung A549 adenocarcinoma, cervix HeLa adenocarcinoma) expand Show data source

DETAILS

DETAILS

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Speiser, P. et al., Experientia, 1947, 3, 323, (isol)
  • • Speiser, P. et al., Helv. Chim. Acta, 1948, 31, 622, (struct)
  • • Lichti, H. et al., Helv. Chim. Acta, 1956, 39, 1914, (Ledienoside, Periplogenin digitoxoside)
  • • Zelnik, R. et al., Helv. Chim. Acta, 1957, 40, 2110
  • • Deghenghi, R. et al., Tet. Lett., 1963, 2045, (synth)
  • • Shoji, J. et al., Chem. Pharm. Bull., 1967, 15, 720, (isol)
  • • Sauer, H.H. et al., Phytochemistry, 1968, 7, 1543, (biosynth)
  • • Kamano, Y. et al., J.C.S. Perkin 1, 1975, 1976, (synth)
  • • Pauli, G.F., Planta Med., 1995, 61, 162, (Periplorhamnoside, Periplogenin glucoside, pmr)
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PATENTS

PATENTS

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INTERNET

INTERNET

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