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2919-66-6 molecular structure
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(1S,2R,10R,11S,14R,15S)-14-acetyl-2,8,15-trimethyl-13-methylidene-5-oxotetracyclo[8.7.0.02,7.011,15]heptadeca-6,8-dien-14-yl acetate

ChemBase ID: 128244
Molecular Formular: C25H32O4
Molecular Mass: 396.51918
Monoisotopic Mass: 396.2300595
SMILES and InChIs

SMILES:
O=C1C=C2C(=C[C@@H]3[C@H](CC[C@@]4([C@](OC(=O)C)(C(=C)C[C@@H]34)C(=O)C)C)[C@@]2(C)CC1)C
Canonical SMILES:
O=C1CC[C@]2(C(=C1)C(=C[C@@H]1[C@@H]2CC[C@]2([C@H]1CC(=C)[C@]2(OC(=O)C)C(=O)C)C)C)C
InChI:
InChI=1S/C25H32O4/c1-14-11-19-20(23(5)9-7-18(28)13-21(14)23)8-10-24(6)22(19)12-15(2)25(24,16(3)26)29-17(4)27/h11,13,19-20,22H,2,7-10,12H2,1,3-6H3/t19-,20+,22+,23-,24+,25+/m1/s1
InChIKey:
UDKABVSQKJNZBH-DWNQPYOZSA-N

Cite this record

CBID:128244 http://www.chembase.cn/molecule-128244.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(1S,2R,10R,11S,14R,15S)-14-acetyl-2,8,15-trimethyl-13-methylidene-5-oxotetracyclo[8.7.0.02,7.011,15]heptadeca-6,8-dien-14-yl acetate
IUPAC Traditional name
melengestrol acetate
Synonyms
17-(Acetyloxy)-6-methyl-16-methylenepregna-4,6-diene-3,20-dione
17-Hydroxy-6-methyl-16-methylenepregna-4,6-diene-3,20-dione Acetate
17-Acetoxy-6-methyl-16-methylenepregna-4,6-diene-3,20-dione
6-Dehydro-16-methylene-17α-hydroxy-6α-methylprogesterone Acetate
Heifermax 500
NSC-70968
MGA
17α-Acetoxy-6-methyl-16-methylene-4,6-pregnadiene-3,20-dione
Melengestrol acetate
Melengestrol acetate
17α-乙酰氧基-6-甲基-16-亚甲基-4,6-孕甾二烯-3,20-二酮
醋酸美伦孕酮
CAS Number
2919-66-6
EC Number
220-859-7
MDL Number
MFCD00072142
Beilstein Number
2066919
PubChem SID
24860753
162222553
24886527
PubChem CID
250948
Chemspider ID
219803
Wikipedia Title
Melengestrol_acetate

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 17.536983  H Acceptors
H Donor LogD (pH = 5.5) 3.819025 
LogD (pH = 7.4) 3.819025  Log P 3.819025 
Molar Refractivity 112.8275 cm3 Polarizability 44.043472 Å3
Polar Surface Area 60.44 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
Chloroform expand Show data source
Ethyl Acetate expand Show data source
Apperance
Light Tan Solid expand Show data source
Melting Point
202-204 °C(lit.) expand Show data source
219-221°C expand Show data source
Storage Condition
Refrigerator expand Show data source
RTECS
TU4141000 expand Show data source
European Hazard Symbols
Harmful Harmful (Xn) expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
62 expand Show data source
Safety Statements
36 expand Show data source
GHS Pictograms
GHS08 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H361 expand Show data source
GHS Precautionary statements
P281 expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves expand Show data source
Eyeshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges expand Show data source
Purity
≥97.0% (HPLC) expand Show data source
Grade
VETRANAL™, analytical standard expand Show data source
Certificate of Analysis
Download expand Show data source
Empirical Formula (Hill Notation)
C25H32O4 expand Show data source

DETAILS

DETAILS

Wikipedia Wikipedia Sigma Aldrich Sigma Aldrich TRC TRC
Sigma Aldrich - 73248 external link
Biochem/physiol Actions
Causes shrinkage of androgen-dependent prostate tumors.1
Sigma Aldrich - 33998 external link
Legal Information
VETRANAL is a trademark of Sigma-Aldrich Co. LLC
Toronto Research Chemicals - M215350 external link
Orally active progestational steroid. Progestogen; growth promotant.

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Patton, M., et al.: Zoo Biol., 26, 311(2007)
  • • Sellin, M., et al.: Environ. Toxicol. Chem., 28, 2443 (2007)
  • • Fliri, A., et al.: J. Med. Chem., 52, 8038 (2007)
  • • Sanseverino, J., et al.: Toxicol. Sci., 107, 122 (2007)
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PATENTS

PATENTS

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INTERNET

INTERNET

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