epi testosterone Search Results


N/A
17-epi-Testosterone-d3(Cat No.:R040406) is a deuterated analog of 17-epi-testosterone, a minor natural metabolite of testosterone. Enhanced with three deuterium atoms, this compound offers improved stability and specificity in analytical testing, particularly in doping control and endocrinological
  Buy from Supplier

93
Santa Cruz Biotechnology 17 epi testosterone d3
17 Epi Testosterone D3, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/epi+testosterone/17-epi-Testosterone-d3/bio_rxiv__2024__06__09__598130-208-44-46
Average 93 stars, based on 1 article reviews
17 epi testosterone d3 - by Bioz Stars, 2026-10
93/100 stars
  Buy from Supplier

88
Santa Cruz Biotechnology 17β methyltestosterone
Reaction scheme for <t>17α-hydroxymethyl-17β-methyl-18-nor-5ξ-androst-13-en-3ξ-ol</t> steroids.
17β Methyltestosterone, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/epi+testosterone/17%CE%B2-Methyl+epi-Testosterone-d5/pmc07961831-178-0-7
Average 88 stars, based on 1 article reviews
17β methyltestosterone - by Bioz Stars, 2026-10
88/100 stars
  Buy from Supplier

88
Cerilliant Corporation epi testosterone
Reaction scheme for <t>17α-hydroxymethyl-17β-methyl-18-nor-5ξ-androst-13-en-3ξ-ol</t> steroids.
Epi Testosterone, supplied by Cerilliant Corporation, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/epi+testosterone/Epitestosterone+(1%2E0+mg%2Fml)+in+Acetonitrile/pmc08620864-84-25-35
Average 88 stars, based on 1 article reviews
epi testosterone - by Bioz Stars, 2026-10
88/100 stars
  Buy from Supplier








Image Search Results


Reaction scheme for 17α-hydroxymethyl-17β-methyl-18-nor-5ξ-androst-13-en-3ξ-ol steroids.

Journal: Molecules

Article Title: New Insights into the Metabolism of Methyltestosterone and Metandienone: Detection of Novel A-Ring Reduced Metabolites

doi: 10.3390/molecules26051354

Figure Lengend Snippet: Reaction scheme for 17α-hydroxymethyl-17β-methyl-18-nor-5ξ-androst-13-en-3ξ-ol steroids.

Article Snippet: 17β-Methyltestosterone (epi-MT, 9 ) was obtained from Santa Cruz Biotechnology (Heidelberg, Germany).

Techniques:

Mass spectrum (GC-EI-QTOF-MS, 70 eV) of 17α-hydroxymethyl-17β-methyl-18-nor-5β-androst-13-en-3α-ol ( 8 ), bis- trimethylsilyl) (TMS (x-axis: m / z ; y-axis: relative abundance).

Journal: Molecules

Article Title: New Insights into the Metabolism of Methyltestosterone and Metandienone: Detection of Novel A-Ring Reduced Metabolites

doi: 10.3390/molecules26051354

Figure Lengend Snippet: Mass spectrum (GC-EI-QTOF-MS, 70 eV) of 17α-hydroxymethyl-17β-methyl-18-nor-5β-androst-13-en-3α-ol ( 8 ), bis- trimethylsilyl) (TMS (x-axis: m / z ; y-axis: relative abundance).

Article Snippet: 17β-Methyltestosterone (epi-MT, 9 ) was obtained from Santa Cruz Biotechnology (Heidelberg, Germany).

Techniques:

Retention times (GC-QQQ-MS), molecular ions (M •+ ) in low electron ionization (LEI, 20 eV), and mass difference to exact mass ( m / z ther 448.3187, C 26 H 48 O 2 Si 2 +• ) of diasteromeric  17α-hydroxymethyl-17β-methyl-18-nor-5ξ-androst-13-en-3ξ-ols  as per-TMS derivatives.

Journal: Molecules

Article Title: New Insights into the Metabolism of Methyltestosterone and Metandienone: Detection of Novel A-Ring Reduced Metabolites

doi: 10.3390/molecules26051354

Figure Lengend Snippet: Retention times (GC-QQQ-MS), molecular ions (M •+ ) in low electron ionization (LEI, 20 eV), and mass difference to exact mass ( m / z ther 448.3187, C 26 H 48 O 2 Si 2 +• ) of diasteromeric 17α-hydroxymethyl-17β-methyl-18-nor-5ξ-androst-13-en-3ξ-ols as per-TMS derivatives.

Article Snippet: 17β-Methyltestosterone (epi-MT, 9 ) was obtained from Santa Cruz Biotechnology (Heidelberg, Germany).

Techniques:

1 H and 13 C NMR spectral data of  17α-hydroxymethyl-17β-methyl-18-nor-5β-androst-13-en-3α-ol  ( 8 ) and 17α-hydroxymethyl-17β-methyl-18-nor-5α-androst-13-en-3α-ol ( 8a ). Multiplicity of signals indicated as singlet (s), doublet (d).

Journal: Molecules

Article Title: New Insights into the Metabolism of Methyltestosterone and Metandienone: Detection of Novel A-Ring Reduced Metabolites

doi: 10.3390/molecules26051354

Figure Lengend Snippet: 1 H and 13 C NMR spectral data of 17α-hydroxymethyl-17β-methyl-18-nor-5β-androst-13-en-3α-ol ( 8 ) and 17α-hydroxymethyl-17β-methyl-18-nor-5α-androst-13-en-3α-ol ( 8a ). Multiplicity of signals indicated as singlet (s), doublet (d).

Article Snippet: 17β-Methyltestosterone (epi-MT, 9 ) was obtained from Santa Cruz Biotechnology (Heidelberg, Germany).

Techniques:

Synthesis route for 17β-methyl-5β-androstane-3α,17α-diol ( 11 ).

Journal: Molecules

Article Title: New Insights into the Metabolism of Methyltestosterone and Metandienone: Detection of Novel A-Ring Reduced Metabolites

doi: 10.3390/molecules26051354

Figure Lengend Snippet: Synthesis route for 17β-methyl-5β-androstane-3α,17α-diol ( 11 ).

Article Snippet: 17β-Methyltestosterone (epi-MT, 9 ) was obtained from Santa Cruz Biotechnology (Heidelberg, Germany).

Techniques:

Mass spectrum (GC-EI-QTOF-MS, 70 eV) of 17β-methyl-5β-androstane-3α,17α-diol ( 11 ), bis TMS (x-axis: m / z ; y-axis: relative abundance).

Journal: Molecules

Article Title: New Insights into the Metabolism of Methyltestosterone and Metandienone: Detection of Novel A-Ring Reduced Metabolites

doi: 10.3390/molecules26051354

Figure Lengend Snippet: Mass spectrum (GC-EI-QTOF-MS, 70 eV) of 17β-methyl-5β-androstane-3α,17α-diol ( 11 ), bis TMS (x-axis: m / z ; y-axis: relative abundance).

Article Snippet: 17β-Methyltestosterone (epi-MT, 9 ) was obtained from Santa Cruz Biotechnology (Heidelberg, Germany).

Techniques:

Retention times (GC-QQQ-MS) and ion transitions of currently targeted metabolites in anti-doping analysis.

Journal: Molecules

Article Title: New Insights into the Metabolism of Methyltestosterone and Metandienone: Detection of Novel A-Ring Reduced Metabolites

doi: 10.3390/molecules26051354

Figure Lengend Snippet: Retention times (GC-QQQ-MS) and ion transitions of currently targeted metabolites in anti-doping analysis.

Article Snippet: 17β-Methyltestosterone (epi-MT, 9 ) was obtained from Santa Cruz Biotechnology (Heidelberg, Germany).

Techniques:

Proposed metabolism of methyltestosterone (black, 18 ) and metandienone (red, 12 ) to the found metabolites 17α-hydroxymethyl-17β-methyl-18-nor-5β-androst-13-en-3α-ol ( 8 ), 17α-hydroxymethyl-17β-methyl-18-nor-5α-androst-13-en-3α-ol ( 8a ), and 17β-methyl-5β-androstane-3α,17α-diol ( 11 ) except last step of metandienone. The question marks represent reactions whose enzymes have not been elucidated yet.

Journal: Molecules

Article Title: New Insights into the Metabolism of Methyltestosterone and Metandienone: Detection of Novel A-Ring Reduced Metabolites

doi: 10.3390/molecules26051354

Figure Lengend Snippet: Proposed metabolism of methyltestosterone (black, 18 ) and metandienone (red, 12 ) to the found metabolites 17α-hydroxymethyl-17β-methyl-18-nor-5β-androst-13-en-3α-ol ( 8 ), 17α-hydroxymethyl-17β-methyl-18-nor-5α-androst-13-en-3α-ol ( 8a ), and 17β-methyl-5β-androstane-3α,17α-diol ( 11 ) except last step of metandienone. The question marks represent reactions whose enzymes have not been elucidated yet.

Article Snippet: 17β-Methyltestosterone (epi-MT, 9 ) was obtained from Santa Cruz Biotechnology (Heidelberg, Germany).

Techniques: