Skip to main content
. 2020 Oct 20;11(10):1229. doi: 10.3390/genes11101229

Table 1.

Steroid intermediates detected during cholesterol bioconversion by N. simplex VKM Ac-2033D.

Number Name Molecular Weight Chemical Structure Number Name Molecular Weight Chemical Structure
V Cholest-4-en-3-one 384 graphic file with name genes-11-01229-i001.jpg VI Cholesta-1,4-dien-3-one 382 graphic file with name genes-11-01229-i002.jpg
VII 26-Hydroxy-cholest-4-en-3-one 400 graphic file with name genes-11-01229-i003.jpg VIII 3-Oxo-cholest-4-en-26-oic acid 414 graphic file with name genes-11-01229-i004.jpg
IX 3-Oxo-cholesta-1,4-dien-26-oic acid 412 graphic file with name genes-11-01229-i005.jpg X 3β-Hydroxy-cholest-5-en-26-oic acid 416 graphic file with name genes-11-01229-i006.jpg
XI Androst-4-en-17β-ol-3-one,
Testosterone
288 graphic file with name genes-11-01229-i007.jpg XII Androsta-1,4-dien-17β-ol-3-one, 1-Dehydrotestosterone 286 graphic file with name genes-11-01229-i008.jpg
XIII Androst-4-ene-9α,17β-diol-3-one, 9α-Hydroxy-testosterone(preliminarily determined) 304 graphic file with name genes-11-01229-i009.jpg