Chemistry:Dimethandrolone dodecylcarbonate

Short description: Chemical compound

Dimethandrolone dodecylcarbonate

Clinical data
Other names	CDB-4730; Dimethandrolone dodecanoylcarbonate; Dimethandrolone 17β-dodecylcarbonate; 7α,11β-Dimethyl-19-nortestosterone 17β-dodecylcarbonate
Routes of administration	By mouth, intramuscular injection
Drug class	Androgen; Anabolic steroid; Progestogen
Identifiers
IUPAC name dodecyl (1S,2R,9R,10R,11S,14S,15S,17S)-9,15,17-trimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadec-6-en-14-yl carbonate
PubChem CID	11605987
ChemSpider	9780743
Chemical and physical data
Formula	C33H54O4
Molar mass	514.791 g·mol−1
3D model (JSmol)	Interactive image
SMILES [H][C@]12CCC(=O)C=C1C[C@@H](C)[C@H]1[C@@H]3CC[C@H](OC(=O)OCCCCCCCCCCCC)[C@@]3(C)C[C@H](C)[C@H]21
InChI InChI=1S/C33H54O4/c1-5-6-7-8-9-10-11-12-13-14-19-36-32(35)37-29-18-17-28-31-23(2)20-25-21-26(34)15-16-27(25)30(31)24(3)22-33(28,29)4/h21,23-24,27-31H,5-20,22H2,1-4H3/t23-,24+,27?,28+,29+,30-,31+,33?/m1/s1 Key:XBTJAJJKGSKQCS-BFKPOJPOSA-N

Dimethandrolone dodecylcarbonate (developmental code name CDB-4730), or dimethandrolone dodecanoylcarbonate, also known as 7α,11β-dimethyl-19-nortestosterone 17β-dodecylcarbonate, is a synthetic and orally active anabolic–androgenic steroid (AAS) and a derivative of nandrolone (19-nortestosterone) which was developed by the Contraceptive Development Branch (CDB) of the National Institute of Child Health and Human Development (NICHD) and has not been marketed at this time. It is an androgen ester – specifically, the C17β dodecylcarbonate ester of dimethandrolone (7α,11β-dimethyl-19-nortestosterone) – and acts as a prodrug of dimethandrolone in the body.

See also

• List of androgen esters