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164227094 molecular structure
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(1R,3S,5Z)-5-{2-[(1R,3aS,4E,7aR)-7a-methyl-1-[(2R,3E,5S)-5-(2H3)methyl-6-methylhept-3-en-2-yl]-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol

ChemBase ID: 171184
Molecular Formular: C28H44O2
Molecular Mass: 412.64776
Monoisotopic Mass: 412.33413065
SMILES and InChIs

SMILES:
C1[C@H](C[C@@H](C(=C)/C/1=C\C=C/1\[C@H]2[C@](CCC1)([C@H](CC2)[C@@H](/C=C/[C@H](C(C)C)C)C)C)O)O
Canonical SMILES:
O[C@H]1C[C@H](O)C(=C)/C(=C\C=C\2/CCC[C@]3([C@H]2CC[C@@H]3[C@@H](/C=C/[C@H](C(C)C)C)C)C)/C1
InChI:
InChI=1S/C28H44O2/c1-18(2)19(3)9-10-20(4)25-13-14-26-22(8-7-15-28(25,26)6)11-12-23-16-24(29)17-27(30)21(23)5/h9-12,18-20,24-27,29-30H,5,7-8,13-17H2,1-4,6H3/b10-9+,22-11+,23-12-/t19-,20-,24-,25-,26+,27+,28-/m1/s1
InChIKey:
HKXBNHCUPKIYDM-MIOKCKKRSA-N

Cite this record

CBID:171184 http://www.chembase.cn/molecule-171184.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(1R,3S,5Z)-5-{2-[(1R,3aS,4E,7aR)-7a-methyl-1-[(2R,3E,5S)-5-(2H3)methyl-6-methylhept-3-en-2-yl]-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol
IUPAC Traditional name
(1R,3S,5Z)-5-{2-[(1R,3aS,4E,7aR)-7a-methyl-1-[(2R,3E,5S)-5-(2H3)methyl-6-methylhept-3-en-2-yl]-hexahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol
Synonyms
(1α,3β,5Z,7E,22E)- 9,10-Secoergosta-5,7,10(19),22-tetraene-1,3-diol-d3
1-Hydroxyergocalciferol-d3
1-Hydroxyvitamin D2-d3
1α-Hydroxyergocalciferol-d3
1α-Hydroxyvitamin D2-d3
Doxercalciferol-d3
Hectorol-d3
TSA 840-d3
1α-Hydroxy Vitamin D2-d3
PubChem SID
164227094
PubChem CID
71749293

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
TRC H995802 external link Add to cart
PubChem 71749293 external link
Data Source Data ID Price
TRC
H995802 external link Add to cart Please log in.
Data Source Data ID
PubChem 71749293 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 14.392874  H Acceptors
H Donor LogD (pH = 5.5) 5.746953 
LogD (pH = 7.4) 5.746953  Log P 5.746953 
Molar Refractivity 130.3616 cm3 Polarizability 50.44043 Å3
Polar Surface Area 40.46 Å2 Rotatable Bonds
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
Chloroform expand Show data source
Ethyl Acetate expand Show data source
Apperance
White to Off-White Solid expand Show data source
Melting Point
118-120°C expand Show data source
Storage Condition
Amber Vial, -86°C Freezer expand Show data source
MSDS Link
Download expand Show data source
Certificate of Analysis
Download expand Show data source

DETAILS

DETAILS

TRC TRC
Toronto Research Chemicals - H995802 external link
Synthetic labelled vitamin D prohormone. A new active Vitamin D analog which inhibits growth of human neuroblastoma. Antihyperparathyroid.

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Liu, G., et al.: Clin. Cancer Res., 9(11)
  • • 4077 (11)
  • • Albert, D., et al.: Arch. Ophthalmol., 122(11)
  • • 1365 (11)
  • • Nagai, J., et al.: Cancer Res., 64, 7910 (11)
  • • Reddy, C., et al.: J. Cell Biochem., 97, 198 (11)
  • • Peng, X., et al.: Carcinogenesis, 28,
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PATENTS

PATENTS

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INTERNET

INTERNET

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