hyodeoxycholic acid
7-deoxyhyocholic acid

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  83-49-8 Hyodeoxycholic acid (HDCA) >98%

Name: (4R)-4-[(3R,5R,6S,8S,9S,10R,13R,14S,17R)-3,6-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid CAS Number: 83-49-8 3D/inchi ECHA EINECS - REACH Pre-Reg: 201-483-2 FDA UNII: 7A33Y6EHYK Nikkaji Web: J4.636A MDL: MFCD00003681 XlogP3-AA: 4.90 (est) Molecular Weight: 392.57960000 Formula: C24 H40 O4 NMR Predictor: Predict (works with chrome, Edge or firefox) Category:information only not used for fragrances or flavors   US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information: Google Scholar: Search Google Books: Search Google Scholar: with word "volatile" Search Google Scholar: with word "flavor" Search Google Scholar: with word "odor" Search Google Patents: Search US Patents: Search EU Patents: Search Pubchem Patents: Search PubMed: Search NCBI: Search   Physical Properties: Food Chemicals Codex Listed: No Soluble in:   water, 59.8 mg/L @ 20 °C (exp)   Organoleptic Properties: Odor and/or flavor descriptions from others (if found).   Cosmetic Information: None found   Suppliers: Alfa Biotechnology For experimental / research use only. Hyodeoxycholic acid 98% BOC Sciences For experimental / research use only. Hyodeoxycholic acid (HDCA) >98% Sigma-Aldrich: Sigma For experimental / research use only. Hyodeoxycholic Acid ≥98% sds   Safety Information: Preferred SDS: View   Hazards identification   Classification of the substance or mixture GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) None found. GHS Label elements, including precautionary statements   Pictogram   Hazard statement(s) None found. Precautionary statement(s) None found. Oral/Parenteral Toxicity: Not determined Dermal Toxicity: Not determined Inhalation Toxicity: Not determined   Safety in Use Information: Category: information only not used for fragrances or flavors Recommendation for hyodeoxycholic acid usage levels up to:   not for fragrance use.   Recommendation for hyodeoxycholic acid flavor usage levels up to:   not for flavor use.   Safety References: EPI System: View ClinicalTrials.gov:search AIDS Citations:Search Cancer Citations:Search Toxicology Citations:Search EPA ACToR:Toxicology Data EPA Substance Registry Services (SRS):Registry Laboratory Chemical Safety Summary :5283820 National Institute of Allergy and Infectious Diseases:Data (4R)-4-[(3R,5R,6S,8S,9S,10R,13R,14S,17R)-3,6-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid Chemidplus:0000083498 RTECS:FZ2050000 for cas# 83-49-8   References:   (4R)-4-[(3R,5R,6S,8S,9S,10R,13R,14S,17R)-3,6-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid NIST Chemistry WebBook: Search Inchi Canada Domestic Sub. List: 83-49-8 Pubchem (cid): 5283820 Pubchem (cas): 83-49-8   Other Information: (IUPAC): Atomic Weights of the Elements 2011 (pdf) Videos: The Periodic Table of Videos tgsc: Atomic Weights use for this web site (IUPAC): Periodic Table of the Elements CHEBI: View CHEMBL: View Metabolomics Database: Search KEGG (GenomeNet): C15517 HMDB (The Human Metabolome Database): HMDB00733 FooDB: FDB022211 Export Tariff Code: 2918.19.9000 ChemSpider: View   Potential Blenders and core components note None Found   Potential Uses: None Found   Occurrence (nature, food, other):note   not found in nature   Synonyms:   cholan-24-oic acid, 3,6-dihydroxy-, (3alpha,5beta,6alpha)- 7- deoxyhyocholic acid (4R)-4-[(3R,5R,6S,8S,9S,10R,13R,14S,17R)-3,6- dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid 3-alpha,6-alpha- dihydroxy-5-beta-cholan-24-oic acid   Articles:   None found yet. Try the PubMed Search.

Notes: A bile acid. Bile acids are steroid acids found predominantly in bile of mammals. The distinction between different bile acids is minute, depends only on presence or absence of hydroxyl groups on positions 3, 7, and 12. Bile acids are physiological detergents that facilitate excretion, absorption, and transport of fats and sterols in the intestine and liver. Bile acids are also steroidal amphipathic molecules derived from the catabolism of cholesterol. They modulate bile flow and lipid secretion, are essential for the absorption of dietary fats and vitamins, and have been implicated in the regulation of all the key enzymes involved in cholesterol homeostasis. Bile acids recirculate through the liver, bile ducts, small intestine and portal vein to form an enterohepatic circuit. They exist as anions at physiological pH and, consequently, require a carrier for transport across the membranes of the enterohepatic tissues. The unique detergent properties of bile acids are essential for the digestion and intestinal absorption of hydrophobic nutrients. Bile acids have potent toxic properties (e.g., membrane disruption) and there are a plethora of mechanisms to limit their accumulation in blood and tissues. (PMID: 11316487, 16037564, 12576301, 11907135) [HMDB]