Dihydrotestosterone
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Basic Info
Common Name | Dihydrotestosterone(F05496) |
2D Structure | |
Description | Dihydrotestosterone is a potent androgenic metabolite of testosterone. Dihydrotestosterone (DHT) is generated by a 5-alpha reduction of testosterone. Unlike testosterone, DHT cannot be aromatized to estradiol therefore DHT is considered a pure androgenic steroid. -- Pubchem; Dihydrotestosterone (DHT) (INN: androstanolone) is a biologically active metabolite of the hormone testosterone, formed primarily in the prostate gland, testes, hair follicles, and adrenal glands by the enzyme 5-alpha-reductase by means of reducing the alpha 4,5 double-bond. Dihydrotestosterone belongs to the class of compounds called androgens, also commonly called androgenic hormones or testoids. DHT is thought to be approximately 30 times more potent than testosterone because of increased affinity to the androgen receptor. -- Wikipedia. |
FRCD ID | F05496 |
CAS Number | 521-18-6 |
PubChem CID | 10635 |
Formula | C19H30O2 |
IUPAC Name | (5S,8R,9S,10S,13S,14S,17S)-17-hydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one |
InChI Key | NVKAWKQGWWIWPM-ABEVXSGRSA-N |
InChI | InChI=1S/C19H30O2/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/h12,14-17,21H,3-11H2,1-2H3/t12-,14-,15-,16-,17-,18-,19-/m0/s1 |
Canonical SMILES | CC12CCC(=O)CC1CCC3C2CCC4(C3CCC4O)C |
Isomeric SMILES | C[C@]12CCC(=O)C[C@@H]1CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CC[C@@H]4O)C |
Wikipedia | Dihydrotestosterone |
Synonyms | STANOLONE dihydrotestosterone Androstanolone 521-18-6 Andractim Androlone Anaboleen Anabolex Proteina Stanaprol |
Classifies | Animal Toxin |
Update Date | Nov 13, 2018 17:07 |
Chemical Taxonomy
Kingdom | Organic compounds |
Superclass | Lipids and lipid-like molecules |
Class | Steroids and steroid derivatives |
Subclass | Androstane steroids |
Intermediate Tree Nodes | Not available |
Direct Parent | Androgens and derivatives |
Alternative Parents | |
Molecular Framework | Aliphatic homopolycyclic compounds |
Substituents | Androgen-skeleton - 3-oxosteroid - 3-oxo-5-alpha-steroid - 17-hydroxysteroid - Oxosteroid - Hydroxysteroid - Cyclic alcohol - Cyclic ketone - Secondary alcohol - Ketone - Organic oxygen compound - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Alcohol - Aliphatic homopolycyclic compound |
Description | This compound belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans. |
Properties
Property Name | Property Value |
---|---|
Molecular Weight | 290.447 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 0 |
Complexity | 459 |
Monoisotopic Mass | 290.225 |
Exact Mass | 290.225 |
XLogP | 3.7 |
Formal Charge | 0 |
Heavy Atom Count | 21 |
Defined Atom Stereocenter Count | 7 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Isotope Atom Count | 0 |
Covalently-Bonded Unit Count | 1 |
ADMET
Model | Result | Probability |
---|---|---|
Absorption | ||
Blood-Brain Barrier | BBB+ | 0.9818 |
Human Intestinal Absorption | HIA+ | 1.0000 |
Caco-2 Permeability | Caco2+ | 0.8846 |
P-glycoprotein Substrate | Substrate | 0.5700 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.5631 |
Non-inhibitor | 0.8460 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.7884 |
Distribution | ||
Subcellular localization | Mitochondria | 0.6935 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.7715 |
CYP450 2D6 Substrate | Non-substrate | 0.9300 |
CYP450 3A4 Substrate | Substrate | 0.7314 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.6853 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.9071 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9710 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.9025 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.8546 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9647 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9444 |
Non-inhibitor | 0.5760 | |
AMES Toxicity | Non AMES toxic | 0.9414 |
Carcinogens | Non-carcinogens | 0.9182 |
Fish Toxicity | High FHMT | 0.9491 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.9388 |
Honey Bee Toxicity | High HBT | 0.7636 |
Biodegradation | Not ready biodegradable | 0.9686 |
Acute Oral Toxicity | III | 0.7855 |
Carcinogenicity (Three-class) | Non-required | 0.5215 |
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -4.0976 | LogS |
Caco-2 Permeability | 1.8611 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 1.9757 | LD50, mol/kg |
Fish Toxicity | 1.4336 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.5436 | pIGC50, ug/L |
References
Title | Journal | Date | Pubmed ID |
---|---|---|---|
Relationships between POPs, biometrics and circulating steroids in male polarbears (Ursus maritimus) from Svalbard. | Environ Pollut | 2017 Nov | 28710978 |
Quisqualis indica Improves Benign Prostatic Hyperplasia by Regulating ProstateCell Proliferation and Apoptosis. | Biol Pharm Bull | 2017 Dec 1 | 28943529 |
Accumulation of Palmitoylcarnitine and Its Effect on Pro-Inflammatory Pathwaysand Calcium Influx in Prostate Cancer. | Prostate | 2016 Oct | 27403764 |
Individual and combined in vitro (anti)androgenic effects of certain foodadditives and cosmetic preservatives. | Toxicol In Vitro | 2016 Apr | 26812027 |
Inhibition of the DHT-induced PSA secretion by Verbascum xanthophoeniceum andSerenoa repens extracts in human LNCaP prostate epithelial cells. | J Ethnopharmacol | 2014 Aug 8 | 24928827 |
Intracellular distribution and biological effects of phytochemicals in a sexsteroid- sensitive model of human prostate adenocarcinoma. | Anticancer Agents Med Chem | 2014 | 24962071 |
Yolk concentrations of hormones and glucose and egg weight and egg dimensions in unincubated chicken eggs, in relation to egg sex and hen body weight. | Gen Comp Endocrinol | 2013 Jun 15 | 23510857 |
Prostatic response to supranutritional selenium supplementation: comparison ofthe target tissue potency of selenomethionine vs. selenium-yeast on markers ofprostatic homeostasis. | Nutrients | 2012 Nov 6 | 23201838 |
Increased muscular dehydroepiandrosterone levels are associated with improvedhyperglycemia in obese rats. | Am J Physiol Endocrinol Metab | 2011 Aug | 21285401 |
Cell viability and PSA secretion assays in LNCaP cells: a tiered in vitroapproach to screen chemicals with a prostate-mediated effect on male reproductionwithin the ReProTect project. | Reprod Toxicol | 2010 Aug | 20363314 |
Diets high in selenium and isoflavones decrease androgen-regulated geneexpression in healthy rat dorsolateral prostate. | Reprod Biol Endocrinol | 2008 Nov 24 | 19025659 |
Effect of bisphenol A, tetrachlorobisphenol A and pentachlorophenol on thetranscriptional activities of androgen receptor-mediated reporter gene. | Food Chem Toxicol | 2006 Nov | 16893599 |
Expression of 3alpha- and 3beta-hydroxy steroid dehydrogenase mRNA in COCs and granulosa cells determines Zearalenone biotransformation. | Toxicol In Vitro | 2006 Jun | 16246520 |
Effects of atrazine on metamorphosis, growth, laryngeal and gonadal development, aromatase activity, and sex steroid concentrations in Xenopus laevis. | Ecotoxicol Environ Saf | 2005 Oct | 16112017 |
Evaluation of a two-generation reproduction toxicity study adding endpoints todetect endocrine disrupting activity using vinclozolin. | J Toxicol Sci | 2005 Dec | 16641540 |
Gender differences of renal CYP-derived eicosanoid synthesis in rats fed ahigh-fat diet. | Am J Hypertens | 2005 Apr | 15831364 |
Sensitive in vitro test systems to determine androgenic/antiandrogenic activity. | Mol Nutr Food Res | 2004 Sep | 15497179 |
Effects of atrazine on metamorphosis, growth, and gonadal development in thegreen frog (Rana clamitans). | J Toxicol Environ Health A | 2004 Jun 25 | 15205037 |
Characterisation of gene expression patterns in 22RV1 cells for determination of environmental androgenic/antiandrogenic compounds. | J Steroid Biochem Mol Biol | 2003 Feb | 12711008 |
Interaction between tris(4-chlorophenyl)methanol and the human androgen receptor in vitro. | Toxicol Lett | 2002 Nov 15 | 12368053 |
Targets
- General Function:
- Zinc ion binding
- Specific Function:
- The steroid hormones and their receptors are involved in the regulation of eukaryotic gene expression and affect cellular proliferation and differentiation in target tissues. Progesterone receptor isoform B (PRB) is involved activation of c-SRC/MAPK signaling on hormone stimulation.Isoform A: inactive in stimulating c-Src/MAPK signaling on hormone stimulation.Isoform 4: Increases mitochondrial membrane potential and cellular respiration upon stimulation by progesterone.
- Gene Name:
- PGR
- Uniprot ID:
- P06401
- Molecular Weight:
- 98979.96 Da
References
- Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]
- General Function:
- Oxygen binding
- Specific Function:
- Catalyzes the formation of aromatic C18 estrogens from C19 androgens.
- Gene Name:
- CYP19A1
- Uniprot ID:
- P11511
- Molecular Weight:
- 57882.48 Da
References
- Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]
- General Function:
- Zinc ion binding
- Specific Function:
- Receptor for glucocorticoids (GC). Has a dual mode of action: as a transcription factor that binds to glucocorticoid response elements (GRE), both for nuclear and mitochondrial DNA, and as a modulator of other transcription factors. Affects inflammatory responses, cellular proliferation and differentiation in target tissues. Could act as a coactivator for STAT5-dependent transcription upon growth hormone (GH) stimulation and could reveal an essential role of hepatic GR in the control of body growth. Involved in chromatin remodeling. May play a negative role in adipogenesis through the regulation of lipolytic and antilipogenic genes expression.
- Gene Name:
- NR3C1
- Uniprot ID:
- P04150
- Molecular Weight:
- 85658.57 Da
References
- Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]
- General Function:
- Zinc ion binding
- Specific Function:
- Nuclear hormone receptor. Binds estrogens with an affinity similar to that of ESR1, and activates expression of reporter genes containing estrogen response elements (ERE) in an estrogen-dependent manner (PubMed:20074560). Isoform beta-cx lacks ligand binding ability and has no or only very low ere binding activity resulting in the loss of ligand-dependent transactivation ability. DNA-binding by ESR1 and ESR2 is rapidly lost at 37 degrees Celsius in the absence of ligand while in the presence of 17 beta-estradiol and 4-hydroxy-tamoxifen loss in DNA-binding at elevated temperature is more gradual.
- Gene Name:
- ESR2
- Uniprot ID:
- Q92731
- Molecular Weight:
- 59215.765 Da
References
- Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]
- General Function:
- Testosterone dehydrogenase (nad+) activity
- Specific Function:
- Favors the reduction of estrogens and androgens. Also has 20-alpha-HSD activity. Uses preferentially NADH.
- Gene Name:
- HSD17B1
- Uniprot ID:
- P14061
- Molecular Weight:
- 34949.715 Da
- General Function:
- Zinc ion binding
- Specific Function:
- Steroid hormone receptors are ligand-activated transcription factors that regulate eukaryotic gene expression and affect cellular proliferation and differentiation in target tissues. Transcription factor activity is modulated by bound coactivator and corepressor proteins. Transcription activation is down-regulated by NR0B2. Activated, but not phosphorylated, by HIPK3 and ZIPK/DAPK3.
- Gene Name:
- AR
- Uniprot ID:
- P10275
- Molecular Weight:
- 98987.9 Da
References
- Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]
- General Function:
- Zinc ion binding
- Specific Function:
- Nuclear hormone receptor. The steroid hormones and their receptors are involved in the regulation of eukaryotic gene expression and affect cellular proliferation and differentiation in target tissues. Ligand-dependent nuclear transactivation involves either direct homodimer binding to a palindromic estrogen response element (ERE) sequence or association with other DNA-binding transcription factors, such as AP-1/c-Jun, c-Fos, ATF-2, Sp1 and Sp3, to mediate ERE-independent signaling. Ligand binding induces a conformational change allowing subsequent or combinatorial association with multiprotein coactivator complexes through LXXLL motifs of their respective components. Mutual transrepression occurs between the estrogen receptor (ER) and NF-kappa-B in a cell-type specific manner. Decreases NF-kappa-B DNA-binding activity and inhibits NF-kappa-B-mediated transcription from the IL6 promoter and displace RELA/p65 and associated coregulators from the promoter. Recruited to the NF-kappa-B response element of the CCL2 and IL8 promoters and can displace CREBBP. Present with NF-kappa-B components RELA/p65 and NFKB1/p50 on ERE sequences. Can also act synergistically with NF-kappa-B to activate transcription involving respective recruitment adjacent response elements; the function involves CREBBP. Can activate the transcriptional activity of TFF1. Also mediates membrane-initiated estrogen signaling involving various kinase cascades. Isoform 3 is involved in activation of NOS3 and endothelial nitric oxide production. Isoforms lacking one or several functional domains are thought to modulate transcriptional activity by competitive ligand or DNA binding and/or heterodimerization with the full length receptor. Essential for MTA1-mediated transcriptional regulation of BRCA1 and BCAS3. Isoform 3 can bind to ERE and inhibit isoform 1.
- Gene Name:
- ESR1
- Uniprot ID:
- P03372
- Molecular Weight:
- 66215.45 Da
References
- Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]