(R,R)-Tetrahydrochrysene
From WikiMD's Wellness Encyclopedia
What is (R,R)-Tetrahydrochrysene? [ edit | edit source ]
It is a drug that binds to Human Estrogen Receptor alpha(ERα) and beta(ERβ) Ligand-binding Domain and used in scientific research. It is agonist to ERα and antagonist to ERβ[1] [2] .
Molecular formula : C22H24O2
Molecular weight : 320.4
IUPAC Name : (5R,11R)-5,11-diethyl-5,6,11,12-tetrahydrochrysene-2,8-diol
Synonyms :
(R,R)-THC
138090-06-9
(R,R)-cis-Diethyl tetrahydro-2,8-chrysenediol
(5R,11R)-5,11-diethyl-5,6,11,12-tetrahydrochrysene-2,8-diol
221368-54-3
CHEMBL282489
(R,R)-5,11-DIETHYL-5,6,11,12-TETRAHYDRO-2,8-CHRYSENEDIOL
(R,R)-cis-Diethyltetrahydro-2,8-chrysenediol
(5R,11R)-5,11-DIETHYL-5,6,11,12-TETRAHYDRO-2,8-CHRYSENEDIOL
(R,R)-5,11-CIS-DIETHYL-5,6,11,12-TETRAHYDROCHRYSENE-2,8-DIOL
5,11-cis-diethyl-5,6,11,12-tetrahydrochrysene-2,8-diol
UNII-JDD6B8E8CW
Lopac-D-8690
JDD6B8E8CW
Lopac0_000463
MLS002153151
BIDD:ER0043
↑
{{{last}}},
Ying Chen,
The Role of Steroids in the Regulation of Oocyte Cyst Breakdown and Primordial Follicle Assembly in the Neonatal Mouse Ovary . online version ,
ProQuest,
2008,
ISBN 978-0-549-74620-1,
Pages: 101–,
↑
,
Structural characterization of a subtype-selective ligand reveals a novel mode of estrogen receptor antagonism ,
Nat. Struct. Biol. ,
2002,
Vol. 9(Issue: 5),
pp. 359–64,
DOI: 10.1038/nsb787 ,
PMID: 11953755 ,
ER
Agonists
Steroidal: 2-Hydroxyestradiol
2-Hydroxyestrone
3-Methyl-19-methyleneandrosta-3,5-dien-17β-ol
3α-Androstanediol
3α,5α-Dihydrolevonorgestrel
3β,5α-Dihydrolevonorgestrel
3α-Hydroxytibolone
3β-Hydroxytibolone
3β-Androstanediol
4-Androstenediol
4-Androstenedione
4-Fluoroestradiol
4-Hydroxyestradiol
4-Hydroxyestrone
4-Methoxyestradiol
4-Methoxyestrone
5-Androstenediol
7-Oxo-DHEA
7α-Hydroxy-DHEA
7α-Methylestradiol
7β-Hydroxyepiandrosterone
8,9-Dehydroestradiol
8,9-Dehydroestrone
8β-VE2
10β,17β-Dihydroxyestra-1,4-dien-3-one (DHED)
11β-Chloromethylestradiol
11β-Methoxyestradiol
15α-Hydroxyestradiol
16-Ketoestradiol
16-Ketoestrone
16α-Fluoroestradiol
16α-Hydroxy-DHEA
16α-Hydroxyestrone
16α-Iodoestradiol
16α-LE2
16β-Hydroxyestrone
16β,17α-Epiestriol (16β-hydroxy-17α-estradiol)
17α-Estradiol (alfatradiol )
17α-Dihydroequilenin
17α-Dihydroequilin
17α-Epiestriol (16α-hydroxy-17α-estradiol)
17α-Ethynyl-3α-androstanediol
17α-Ethynyl-3β-androstanediol
17β-Dihydroequilenin
17β-Dihydroequilin
17β-Methyl-17α-dihydroequilenin
Abiraterone
Abiraterone acetate
Alestramustine
Almestrone
Anabolic steroids (e.g., testosterone and esters , methyltestosterone , metandienone (methandrostenolone) , nandrolone and esters , many others; via estrogenic metabolites)
Atrimustine
Bolandiol
Bolandiol dipropionate
Butolame
Clomestrone
Cloxestradiol
Conjugated estriol
Conjugated estrogens
Cyclodiol
Cyclotriol
DHEA
DHEA-S
ent -Estradiol
Epiestriol (16β-epiestriol, 16β-hydroxy-17β-estradiol)
Epimestrol
Equilenin
Equilin
ERA-63 (ORG-37663)
Esterified estrogens
Estetrol
Estradiol
Estramustine
Estramustine phosphate
Estrapronicate
Estrazinol
Estriol
Estrofurate
Estrogenic substances
Estromustine
Estrone
Etamestrol (eptamestrol)
Ethinylandrostenediol
Ethinylestradiol
Ethinylestriol
Ethylestradiol
Etynodiol
Etynodiol diacetate
Hexolame
Hippulin
Hydroxyestrone diacetate
Lynestrenol
Lynestrenol phenylpropionate
Mestranol
Methylestradiol
Moxestrol
Mytatrienediol
Nilestriol
Norethisterone
Noretynodrel
Orestrate
Pentolame
Prodiame
Prolame
Promestriene
RU-16117
Quinestradol
Quinestrol
Tibolone
Xenoestrogens: Anise -related (e.g., anethole , anol , dianethole , dianol , photoanethole )
Chalconoids (e.g., isoliquiritigenin , phloretin , phlorizin (phloridzin) , wedelolactone )
Coumestans (e.g., coumestrol , psoralidin )
Flavonoids (incl. 7,8-DHF , 8-prenylnaringenin , apigenin , baicalein , baicalin , biochanin A , calycosin , catechin , daidzein , daidzin , ECG , EGCG , epicatechin , equol , formononetin , glabrene , glabridin , genistein , genistin , glycitein , kaempferol , liquiritigenin , mirificin , myricetin , naringenin , penduletin , pinocembrin , prunetin , puerarin , quercetin , tectoridin , tectorigenin )
Lavender oil
Lignans (e.g., enterodiol , enterolactone , nyasol (cis -hinokiresinol) )
Metalloestrogens (e.g., cadmium )
Pesticides (e.g., alternariol , dieldrin , endosulfan , fenarimol , HPTE , methiocarb , methoxychlor , triclocarban , triclosan )
Phytosteroids (e.g., digitoxin (digitalis ), diosgenin , guggulsterone )
Phytosterols (e.g., β-sitosterol , campesterol , stigmasterol )
Resorcylic acid lactones (e.g., zearalanone , α-zearalenol , β-zearalenol , zearalenone , zeranol (α-zearalanol) , taleranol (teranol, β-zearalanol) )
Steroid -like (e.g., deoxymiroestrol , miroestrol )
Stilbenoids (e.g., resveratrol , rhaponticin )
Synthetic xenoestrogens (e.g., alkylphenols , bisphenols (e.g., BPA , BPF , BPS ), DDT , parabens , PBBs , PHBA , phthalates , PCBs )
Others (e.g., agnuside , rotundifuran )
Mixed (SERMs
) Antagonists
Coregulator-binding modulators: ERX-11
GPER
Agonists Antagonists Unknown
Translate this page: - East Asian
中文 ,
日本 ,
한국어 ,
South Asian
हिन्दी ,
தமிழ் ,
తెలుగు ,
Urdu ,
ಕನ್ನಡ ,
Southeast Asian
Indonesian ,
Vietnamese ,
Thai ,
မြန်မာဘာသာ ,
বাংলা
European
español ,
Deutsch ,
français ,
Greek ,
português do Brasil ,
polski ,
română ,
русский ,
Nederlands ,
norsk ,
svenska ,
suomi ,
Italian
Middle Eastern & African
عربى ,
Turkish ,
Persian ,
Hebrew ,
Afrikaans ,
isiZulu ,
Kiswahili ,
Other
Bulgarian ,
Hungarian ,
Czech ,
Swedish ,
മലയാളം ,
मराठी ,
ਪੰਜਾਬੀ ,
ગુજરાતી ,
Portuguese ,
Ukrainian
Medical Disclaimer : WikiMD is not a substitute for professional medical advice . The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD . If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer .
Credits :Most images are courtesy of Wikimedia commons , and templates Wikipedia , licensed under CC BY SA or similar.