CHEBI:28324 - 11-deoxycortisol

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 11-deoxycortisol
ChEBI ID CHEBI:28324
Definition A deoxycortisol that is cortisol in which the hydroxy group at position 11 has been replaced by a hydrogen.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:19124, CHEBI:714
Supplier Information ChemicalBook:CB3238150, eMolecules:524834, ZINC000003777423
Download Molfile XML SDF
more structures >>
Wikipedia License
Heroin, also known as diacetylmorphine and diamorphine among other names, is a morphinan opioid substance synthesized from the dried latex of the opium poppy; it is mainly used as a recreational drug for its euphoric effects. Heroin is used medically in several countries to relieve pain, such as during childbirth or a heart attack, as well as in opioid replacement therapy. Medical-grade diamorphine is used as a pure hydrochloride salt. Various white and brown powders sold illegally around the world as heroin are routinely diluted with cutting agents. Black tar heroin is a variable admixture of morphine derivatives—predominantly 6-MAM (6-monoacetylmorphine), which is the result of crude acetylation during clandestine production of street heroin. Heroin is typically injected, usually into a vein, but it can also be snorted, smoked, or inhaled. In a clinical context, the route of administration is most commonly intravenous injection; it may also be given by intramuscular or subcutaneous injection, as well as orally in the form of tablets. The onset of effects is usually rapid and lasts for a few hours. Common side effects include respiratory depression (decreased breathing), dry mouth, drowsiness, impaired mental function, constipation, and addiction. Use by injection can also result in abscesses, infected heart valves, blood-borne infections, and pneumonia. After a history of long-term use, opioid withdrawal symptoms can begin within hours of the last use. When given by injection into a vein, heroin has two to three times the effect of a similar dose of morphine. It typically appears in the form of a white or brown powder. Treatment of heroin addiction often includes behavioral therapy and medications. Medications can include buprenorphine, methadone, or naltrexone. A heroin overdose may be treated with naloxone. As of 2015, an estimated 17 million people use opiates, of which heroin is the most common, and opioid use resulted in 122,000 deaths; also, as of 2015, the total number of heroin users worldwide is believed to have increased in Africa, the Americas, and Asia since 2000. In the United States, approximately 1.6 percent of people have used heroin at some point. When people die from overdosing on a drug, the drug is usually an opioid and often heroin. Heroin was first made by C. R. Alder Wright in 1874 from morphine, a natural product of the opium poppy. Internationally, heroin is controlled under Schedules I and IV of the Single Convention on Narcotic Drugs, and it is generally illegal to make, possess, or sell without a license. About 448 tons of heroin were made in 2016. In 2015, Afghanistan produced about 66% of the world's opium. Illegal heroin is often mixed with other substances such as sugar, starch, caffeine, quinine, or other opioids like fentanyl.
Read full article at Wikipedia
Formula C21H30O4
Net Charge 0
Average Mass 346.46050
Monoisotopic Mass 346.21441
InChI InChI=1S/C21H30O4/c1-19-8-5-14(23)11-13(19)3-4-15-16(19)6-9-20(2)17(15)7-10-21(20,25)18(24)12-22/h11,15-17,22,25H,3-10,12H2,1-2H3/t15-,16+,17+,19+,20+,21+/m1/s1
InChIKey WHBHBVVOGNECLV-OBQKJFGGSA-N
SMILES [H][C@@]12CCC3=CC(=O)CC[C@]3(C)[C@@]1([H])CC[C@@]1(C)[C@@]2([H])CC[C@]1(O)C(=O)CO
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Homo sapiens (NCBI:txid9606) See: DOI
Roles Classification
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
hormone
Originally referring to an endogenous compound that is formed in specialized organ or group of cells and carried to another organ or group of cells, in the same organism, upon which it has a specific regulatory function, the term is now commonly used to include non-endogenous, semi-synthetic and fully synthetic analogues of such compounds.
(via steroid hormone )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 11-deoxycortisol (CHEBI:28324) has role human metabolite (CHEBI:77746)
11-deoxycortisol (CHEBI:28324) has role mouse metabolite (CHEBI:75771)
11-deoxycortisol (CHEBI:28324) is a deoxycortisol (CHEBI:23618)
11-deoxycortisol (CHEBI:28324) is a glucocorticoid (CHEBI:24261)
11-deoxycortisol (CHEBI:28324) is a primary α-hydroxy ketone (CHEBI:139590)
11-deoxycortisol (CHEBI:28324) is a tertiary α-hydroxy ketone (CHEBI:139592)
IUPAC Name
17,21-dihydroxypregn-4-ene-3,20-dione
Synonyms Sources
11-Deoxycortisol KEGG COMPOUND
11-deoxycortisol UniProt
11-desoxy-17-hydroxycorticosterone ChemIDplus
cortodoxone ChemIDplus
Cortodoxone KEGG COMPOUND
Manual Xrefs Databases
C05488 KEGG COMPOUND
Cortexolone Wikipedia
D03595 KEGG DRUG
HMDB0000015 HMDB
LMST02030086 LIPID MAPS
View more database links
Registry Numbers Types Sources
152-58-9 CAS Registry Number KEGG COMPOUND
152-58-9 CAS Registry Number ChemIDplus
2511358 Reaxys Registry Number Reaxys
Citations Types Sources
18958601 PubMed citation Europe PMC
24863084 PubMed citation Europe PMC
Last Modified
06 February 2018