Deoxycholic acid structure
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Common Name | Deoxycholic acid | ||
|---|---|---|---|---|
| CAS Number | 83-44-3 | Molecular Weight | 392.572 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 547.1±35.0 °C at 760 mmHg | |
| Molecular Formula | C24H40O4 | Melting Point | 171-174 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 298.8±22.4 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of Deoxycholic acidDeoxycholic acid is specifically responsible for activating the G protein-coupled bile acid receptor TGR5 that stimulates brown adipose tissue (BAT) thermogenic activity. |
This table lists Chinese names, IUPAC names and various aliases of this chemical substance.
| Name | Deoxycholic Acid |
|---|---|
| Synonym | More Synonyms |
This table contains bioactivity, target information and biological‑assay experimental data of this compound.
| Description | Deoxycholic acid is specifically responsible for activating the G protein-coupled bile acid receptor TGR5 that stimulates brown adipose tissue (BAT) thermogenic activity. |
|---|---|
| Related Catalog | |
| Target |
Human Endogenous Metabolite |
| In Vitro | Deoxycholic acid (DCA) and chenoDeoxycholic acid (CDCA), as the common ingredients of duodenal reflux, act synergistically in many physiological and pathological processes. The cells are repeatedly exposed to 100 μM CDCA and Deoxycholic acid at pH 5.5 for up to 120 min. To simulate chronic local recurrent disease in vitro, the gastric cancer cell line MGC803 is exposed to acidified medium (pH 5.5) containing 100 μM Deoxycholic acid and CDCA. An untreated log-growth MGC803 cell line is generated to be used as a control in normal pH media. After daily 10 min exposure to the acidified bile acids for 60 weeks, MGC803-resistant cells are able to survive and proliferate after 120 min exposure[2]. |
| Cell Assay | MGC803 cells are cultured in Roswell Park Memorial Institute media supplemented with 10% fetal calf serum and 100 U/mL Penicillin and 100 mg/mL Streptomycin. To generate MGC803-resistant cells, the pH value of the MGC803 culture medium is adjusted to the experimental conditions using the hydrochloric acid (A). The bile acids GCDA and Deoxycholic acid are diluted to optimal working concentrations of 100 μM (B) with culture medium, and the overall pH (A+B) is adjusted to pH 5.5, simulating the gastric environment. Initially, MGC803 cells are chronically exposed to acidified medium with bile acids (A+B) for 10 min every 24 h. The experimental time and conditions are optimized in our preliminary experiments, which show that 10 min is enough and does not result in cell damage. This procedure is repeated and it takes 60 weeks for the MGC803 cells to survive and proliferate under the exposure of A+B for 120 min. Control untreated cells are cultured in neutral RPMI medium at pH 7.4 in parallel to the resistant cells for 60 weeks. The morphological changes in MGC803 cells exposed to acidified bile acids (A+B) are documented at 30 and 60 weeks[2]. |
| References |
This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.
| Density | 1.1±0.1 g/cm3 |
|---|---|
| Boiling Point | 547.1±35.0 °C at 760 mmHg |
| Melting Point | 171-174 °C(lit.) |
| Molecular Formula | C24H40O4 |
| Molecular Weight | 392.572 |
| Flash Point | 298.8±22.4 °C |
| Exact Mass | 392.292664 |
| PSA | 77.76000 |
| LogP | 4.66 |
| Vapour Pressure | 0.0±3.3 mmHg at 25°C |
| Index of Refraction | 1.543 |
| InChIKey | KXGVEGMKQFWNSR-LLQZFEROSA-N |
| SMILES | CC(CCC(=O)O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12C |
| Water Solubility | 0.24 g/L (15 ºC) |
This table provides MSDS information including hazard classification, first‑aid, fire‑fighting, spill handling, operation and storage instructions.
This table summarizes toxicological test data, acute & chronic toxicity and ecological hazard parameters for this chemical.
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302 |
| Precautionary Statements | P301 + P312 + P330 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | Xn:Harmful |
| Risk Phrases | R22;R36/37/38 |
| Safety Phrases | S26-S36-S37/39 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| RTECS | FZ2100000 |
This table presents publicly reported synthetic routes, reaction conditions, reactants and product information of the compound.
This table lists upstream starting materials and downstream derivative products related to this chemical.
| Precursor 9 | |
|---|---|
| DownStream 8 | |
This table lists relevant public references with title, journal and publication metadata for this compound.
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MicroRNA-99a and 100 mediated upregulation of FOXA1 in bladder cancer.
Oncotarget 5(15) , 6375-86, (2014) Urothelial cell carcinoma of the bladder (UCC) is a common disease often characterized by FGFR3 dysregulation. Whilst upregulation of this oncogene occurs most frequently in low-grade non-invasive tum... |
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Involvement of epigenetics and EMT-related miRNA in arsenic-induced neoplastic transformation and their potential clinical use.
Cancer Prev. Res. (Phila.) 8(3) , 208-21, (2015) Exposure to toxicants leads to cumulative molecular changes that overtime increase a subject's risk of developing urothelial carcinoma. To assess the impact of arsenic exposure at a time progressive m... |
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MicroRNA expression profiles associated with acquired gefitinib-resistance in human lung adenocarcinoma cells.
Mol. Med. Report. 11(1) , 333-40, (2014) The aim of the present study was to establish, characterize and elucidate the potential mechanisms of acquired gefitinb resistance, using the A549 human lung cancer cell line. A gefitinib-resistant A5... |
This table contains target information, in‑vitro & in‑vivo assay data for this compound.
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Name: TP_TRANSPORTER: inhibition of Taurocholate uptake (Taurocholate: 0.72 uM, Deoxycholat...
Source: ChEMBL
Target: Ileal sodium/bile acid cotransporter
External Id: CHEMBL2076337
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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Name: Thermal Shift Assay. Domain: start/stop: M1-L298
Source: ChEMBL
Target: Cyclin-dependent kinase 2
External Id: CHEMBL5062802
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify pos...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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Name: TP_TRANSPORTER: uptake of Deoxycholate at 1 uM in Oatp1-expressing HeLa cells
Source: ChEMBL
Target: Solute carrier organic anion transporter family member 1A1
External Id: CHEMBL2076349
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Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id: SIAE_INH_FP_1536_1X%INH PRUN
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Name: Counterscreen for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberc...
Source: The Scripps Research Institute Molecular Screening Center
Target: N/A
External Id: GDH-TPI_INH_ABS_1536_1X%INH CSRUN
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Name: Hedgehog Measured in Biochemical System Using Plate Reader - 2070-01_Inhibitor_Single...
Source: Broad Institute
Target: hedgehog, isoform A [Drosophila melanogaster]
External Id: 2070-01_Inhibitor_SinglePoint_HTS_Activity
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Name: TP_TRANSPORTER: inhibition of BSP uptake (BSP: 2 uM, DCA: 100 uM) in Xenopus laevis o...
Source: ChEMBL
Target: Solute carrier organic anion transporter family member 1A1
External Id: CHEMBL2076362
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This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.
| 7-DEOXYCHOLIC ACID |
| 5b-Deoxycholic acid |
| Deoxycholatic acid |
| EINECS 201-478-5 |
| Deoxycholic acid |
| 17b-(1-Methyl-3-carboxypropyl)etiocholane-3a,12a-diol |
| deoxy-Cholic acid |
| (3α,5β,12α)-3,12-Dihydroxycholan-24-oic acid |
| 7α-Deoxycholic acid |
| Kybella |
| 3α,12α-dihydroxy-5β-cholan-24-oic acid |
| ATX-101 |
| 5b-Cholanic acid-3a,12a-diol |
| Dihydroxycholanoic acid |
| (3a,5b,12a)-3,12-Dihydroxy-5-cholan-24-oic Acid |
| (4R)-4-[(3R,5R,8R,9S,10S,12S,13R,14S,17R)-3,12-Dihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid |
| MFCD00003673 |
This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.
| Q: What is the English name of Deoxycholic Acid? |
| A: The English name of Deoxycholic Acid is Deoxycholic Acid. |
| Q: What is the LogP of Deoxycholic Acid? |
| A: LogP of Deoxycholic Acid is 4.66. |
| Q: What are the uses of Deoxycholic Acid? |
| A: Main uses of Deoxycholic Acid: Deoxycholic acid is specifically responsible for activating the G protein-coupled bile acid receptor TGR5 that stimulates brown adipose tissue (BAT) thermogenic activity. |
| Q: What are the upstream materials of Deoxycholic Acid? |
| A: Related upstream materials(CAS) of Deoxycholic Acid: 3245-38-3;28050-47-7;27240-83-1;434-13-9;4472-02-0;560-62-3;1093397-61-5;1093397-63-7;571-49-3. |
| Q: What is the polar surface area (PSA) of Deoxycholic Acid? |
| A: Polar surface area (PSA) of Deoxycholic Acid is 77.76000. |
| Q: What are the downstream products of Deoxycholic Acid? |
| A: Related downstream products(CAS) of Deoxycholic Acid: 360-65-6;3245-38-3;15173-30-5;434-13-9;513-49-5;2287-93-6;2387-23-7;516-50-7. |
| Q: What is the melting point of Deoxycholic Acid? |
| A: Melting point of Deoxycholic Acid is 171-174 °C(lit.). |
| Q: How is the water solubility of Deoxycholic Acid? |
| A: Water solubility of Deoxycholic Acid: 0.24 g/L (15 ºC). |
| Q: What is the molecular weight of Deoxycholic Acid? |
| A: Molecular weight of Deoxycholic Acid is 392.572. |
| Q: What is the InChIKey of Deoxycholic Acid? |
| A: InChIKey of Deoxycholic Acid is KXGVEGMKQFWNSR-LLQZFEROSA-N. |
This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.
| Shanghai Nianxing Industrial Co., Ltd |
| BioBioPha |
| Dayang Chem (Hangzhou) Co., Ltd. |
| Henan Tianfu Chemical Co., Ltd. |
| Zhongshan Xingrui Chemical Co. , Ltd. |