4-Androstenedione

Form a molecule model of 4-Androstenedione utilizing Genuine Molymod Components by Indigo Instruments

Androstenedione has a chemical structure similar to testosterone, with a four-ring steroid backbone and is synthesized in the adrenal glands and gonads. Androstenedione is a precursor compound that is converted into more potent hormones such as testosterone and estradiol. It also plays an important metabolic role in the development of secondary sexual characteristics and reproductive functions.

A molecular model of 4-Androstenedione in the Molymod Hybrid Dome style uses the atoms & bonds in the parts list below. Our free 3D Molecular Model Builder shows other styles & allows for image rotation as an assembly guide.

Chemical data
Molecular Weight Chemical Formula
286.4132 C19H26O2

4-Androstenedione molecular model built with Molymod Atoms & Bonds

Hybrid Dome
62053
Open Sphere
62009
Orbit Basic
68845NV
Orbit Flexible
68827W 68847W
Parts Synonyms
Parts
P/NDescriptionQTY
60150EAtom, Molymod, white (hydrogen), hemisphere, 19mm26
60200EAtom, Molymod, red (oxygen), 2 hole, 105 degrees2
60400EAtom, Molymod, black (carbon), 4 hole, 109.5 degrees, 23mm19
61012EBond, Molymod, grey (single), 20mm21
61013EBond, Molymod, grey (double/triple), 35mm6
61015EBond, Molymod, opaque, 2mm (for spacefilling models)26
Synonyms
IUPAC Name: (8R,9S,10R,13S,14S)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17-dione , InChI=1S/C19H26O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-16H,3-10H2,1-2H3/t14-,15-,16-,18-,19-/m0/s1 , InChIKey: AEMFNILZOJDQLW-QAGGRKNESA-N , SMILES: CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4=O)C , CAS: 63-05-8 , ,