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H-059

6β-Hydroxytestosterone solution

Name: 6β-Hydroxytestosterone solution
Brand: CERILLIAN

100 μg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant^®

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About This Item

Empirical Formula (Hill Notation):

C₁₉H₂₈O₃

CAS Number:

62-99-7

Molecular Weight:

304.42

EC Number:

200-659-6

MDL number:

MFCD00171612

UNSPSC Code:

41116107

PubChem Substance ID:

329815121

NACRES:

NA.24

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4′-Hydroxydiclofenac

Sigma-Aldrich

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grade

certified reference material

form

liquid

feature

Snap-N-Spike^®/Snap-N-Shoot^®

packaging

ampule of 1 mL

manufacturer/tradename

Cerilliant^®

concentration

100 μg/mL in methanol

technique(s)

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

application(s)

clinical testing

format

single component solution

storage temp.

−20°C

SMILES string

C[C@]12CC[C@H]3[C@@H](C[C@@H](O)C4=CC(=O)CC[C@]34C)[C@@H]1CC[C@@H]2O

InChI

1S/C19H28O3/c1-18-7-5-11(20)9-15(18)16(21)10-12-13-3-4-17(22)19(13,2)8-6-14(12)18/h9,12-14,16-17,21-22H,3-8,10H2,1-2H3/t12-,13-,14-,16+,17-,18+,19-/m0/s1

InChI key

XSEGWEUVSZRCBC-ZVBLRVHNSA-N

General description

A Certified Spiking Solution^® suitable for use as starting material in calibrators or controls for a variety of LC/MS or GC/MS applications from clinical and diagnostic testing to endocrinology and sports testing. 6ß-Hydroxytestosterone is a major urinary metabolite of testosterone, a hormone from the androgen group of steroids. Testosterone is an important sex hormone and anabolic steroid used as a performance-enhancing drug.

Application

Investigating enzyme inhibition with 6β-Hydroxytestosterone: The study on liver microsomal bioreactors for rapid drug metabolism and inhibition assays employed 6β-Hydroxytestosterone to understand its effects on CYP450 enzyme activities, highlighting its utility in pharmacokinetic studies and enzyme behavior under varying physiological conditions (Walgama et al., 2015).

6β-Hydroxytestosterone as a biochemical assay reagent: A sensitive and specific LC-MS/MS cocktail assay developed for CYP450 enzymes employed 6β-Hydroxytestosterone as a reference compound, demonstrating its applicability in biochemical assays and its role in enhancing the detection of enzymatic activity and metabolic pathways (Nguyen et al., 2020).

Legal Information

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany

CERTIFIED SPIKING SOLUTION is a registered trademark of Cerilliant Corporation

Snap-N-Shoot is a registered trademark of Cerilliant Corporation

Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

related product

Product No.

Description

Pricing

Signal Word

Danger

Hazard Statements

H225,H301 + H311 + H331,H370

Precautionary Statements

P210 - P233 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Target Organs

Eyes

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

49.5 °F - closed cup

Flash Point(C)

9.7 °C - closed cup

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Quantitative prediction of macrolide drug-drug interaction potential from in vitro studies using testosterone as the human cytochrome P4503A substrate.

Thomas M Polasek et al.

European journal of clinical pharmacology, 62(3), 203-208 (2006-01-18)

Macrolide antibiotics are mechanism-based inactivators of CYP3A enzymes that exhibit varying degrees of inhibitory potency. Our aim was to predict quantitatively the drug-drug interaction (DDI) potential of five macrolides from in vitro studies using testosterone as the CYP3A substrate, and

The fallacy of using adrenochrome reaction for measurement of reactive oxygen species formed during cytochrome p450-mediated metabolism of xenobiotics.

Cuiping Chen et al.

The Journal of pharmacology and experimental therapeutics, 300(2), 417-420 (2002-01-24)

The adrenochrome reaction (oxidation of epinephrine to adrenochrome) has been widely employed as a standard assay for reactive oxygen species, produced under a variety of conditions, including those produced during cytochrome P450 (CYP)-mediated oxidation of substrates such as cyclosporine. However

The combination of chemical and antibody inhibitors for superior P450 3A inhibition in reaction phenotyping studies.

Dan A Rock et al.

Drug metabolism and disposition: the biological fate of chemicals, 36(12), 2410-2413 (2008-09-04)

Cytochrome P450 (P450) reaction phenotyping is a key process toward accurately determining the contribution of different P450s to the metabolism of new chemical entities. The significance of P450s to drug disposition has led to the identification of selective chemical and

Effects of green tea compounds on irinotecan metabolism.

Snezana Mirkov et al.

Drug metabolism and disposition: the biological fate of chemicals, 35(2), 228-233 (2006-11-17)

The effects of green tea compounds on the metabolism of irinotecan have never been investigated. We aimed to study whether catechins [(-)-epigallocatechin gallate (EGCG), (-)-epicatechin gallate (ECG), (-)-epigallocatechin (EGC), (-)-epicatechin] affect the inactivation metabolism of irinotecan into 7-ethyl-10-[4-N-(1-piperidino)-1-amino]carbonyloxycamptothecin (NPC) (by

Autoinduction of MKC-963 [(R)-1-(1-cyclohexylethylamino)-4-phenylphthalazine] metabolism in healthy volunteers and its retrospective evaluation using primary human hepatocytes and cDNA-expressed enzymes.

Toshiyuki Shimizu et al.

Drug metabolism and disposition: the biological fate of chemicals, 34(6), 950-954 (2006-03-15)

MKC-963, (R)-1-(1-cyclohexylethylamino)-4-phenylphthalazine, a potent inhibitor of platelet aggregation, was synthesized and used in clinical trials in the 1990s. In the process of clinical study, it was found that urinary excretion ratios for 6beta-hydroxycortisol and free cortisol increased significantly in parallel

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