Record Information |
---|
Version | 5.0 |
---|
Status | Expected but not Quantified |
---|
Creation Date | 2005-11-16 15:48:42 UTC |
---|
Update Date | 2022-03-07 02:49:05 UTC |
---|
HMDB ID | HMDB0000659 |
---|
Secondary Accession Numbers | |
---|
Metabolite Identification |
---|
Common Name | Deoxycholic acid disulfate |
---|
Description | Deoxycholic acid disulfate, also known as deoxycholate disulphate, belongs to the class of organic compounds known as bile acids, alcohols and derivatives. These are organic compounds containing an alcohol or acid derivative of cholic acid. Deoxycholic acid disulfate is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. |
---|
Structure | [H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@H](C[C@@]1([H])[C@@]2([H])CC[C@]2([H])C[C@@H](CC[C@]12C)OS(O)(=O)=O)OS(O)(=O)=O InChI=1S/C24H40O10S2/c1-14(4-9-22(25)26)18-7-8-19-17-6-5-15-12-16(33-35(27,28)29)10-11-23(15,2)20(17)13-21(24(18,19)3)34-36(30,31)32/h14-21H,4-13H2,1-3H3,(H,25,26)(H,27,28,29)(H,30,31,32)/t14-,15-,16-,17+,18-,19+,20+,21+,23+,24-/m1/s1 |
---|
Synonyms | Value | Source |
---|
Deoxycholate disulfate | Generator | Deoxycholate disulphate | Generator | Deoxycholic acid disulfuric acid | Generator | Deoxycholic acid disulphuric acid | Generator | Deoxycholic acid disulphate | HMDB |
|
---|
Chemical Formula | C24H40O10S2 |
---|
Average Molecular Weight | 552.698 |
---|
Monoisotopic Molecular Weight | 552.20628888 |
---|
IUPAC Name | (4R)-4-[(1S,2S,5R,7R,10R,11S,14R,15R,16S)-2,15-dimethyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid |
---|
Traditional Name | (4R)-4-[(1S,2S,5R,7R,10R,11S,14R,15R,16S)-2,15-dimethyl-5,16-bis(sulfooxy)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid |
---|
CAS Registry Number | 67030-51-7 |
---|
SMILES | [H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@H](C[C@@]1([H])[C@@]2([H])CC[C@]2([H])C[C@@H](CC[C@]12C)OS(O)(=O)=O)OS(O)(=O)=O |
---|
InChI Identifier | InChI=1S/C24H40O10S2/c1-14(4-9-22(25)26)18-7-8-19-17-6-5-15-12-16(33-35(27,28)29)10-11-23(15,2)20(17)13-21(24(18,19)3)34-36(30,31)32/h14-21H,4-13H2,1-3H3,(H,25,26)(H,27,28,29)(H,30,31,32)/t14-,15-,16-,17+,18-,19+,20+,21+,23+,24-/m1/s1 |
---|
InChI Key | BYHNMIVTBIJJFZ-LLQZFEROSA-N |
---|
Chemical Taxonomy |
---|
Description | Belongs to the class of organic compounds known as bile acids, alcohols and derivatives. These are organic compounds containing an alcohol or acid derivative of cholic acid. |
---|
Kingdom | Organic compounds |
---|
Super Class | Lipids and lipid-like molecules |
---|
Class | Steroids and steroid derivatives |
---|
Sub Class | Bile acids, alcohols and derivatives |
---|
Direct Parent | Bile acids, alcohols and derivatives |
---|
Alternative Parents | |
---|
Substituents | - Bile acid, alcohol, or derivatives
- Sulfated steroid skeleton
- Sulfuric acid monoester
- Sulfate-ester
- Alkyl sulfate
- Sulfuric acid ester
- Organic sulfuric acid or derivatives
- Monocarboxylic acid or derivatives
- Carboxylic acid
- Carboxylic acid derivative
- Organic oxide
- Organooxygen compound
- Organic oxygen compound
- Carbonyl group
- Hydrocarbon derivative
- Aliphatic homopolycyclic compound
|
---|
Molecular Framework | Aliphatic homopolycyclic compounds |
---|
External Descriptors | |
---|
Ontology |
---|
Physiological effect | Not Available |
---|
Disposition | |
---|
Process | |
---|
Role | |
---|
Physical Properties |
---|
State | Solid |
---|
Experimental Molecular Properties | Property | Value | Reference |
---|
Melting Point | Not Available | Not Available | Boiling Point | Not Available | Not Available | Water Solubility | Not Available | Not Available | LogP | Not Available | Not Available |
|
---|
Experimental Chromatographic Properties | Not Available |
---|
Predicted Molecular Properties | | Show more...
---|
Predicted Chromatographic Properties | Predicted Collision Cross SectionsPredicted Kovats Retention IndicesUnderivatizedDerivatizedDerivative Name / Structure | SMILES | Kovats RI Value | Column Type | Reference |
---|
Deoxycholic acid disulfate,1TMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O)[C@@]21C | 4041.1 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,1TMS,isomer #2 | C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O)[C@@]21C | 4088.4 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,1TMS,isomer #3 | C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C)[C@@]21C | 4103.9 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,2TMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O)[C@@]21C | 4014.9 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,2TMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O)[C@@]21C | 4469.3 | Standard non polar | 33892256 | Deoxycholic acid disulfate,2TMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O)[C@@]21C | 5454.4 | Standard polar | 33892256 | Deoxycholic acid disulfate,2TMS,isomer #2 | C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C)[C@@]21C | 4026.8 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,2TMS,isomer #2 | C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C)[C@@]21C | 4460.0 | Standard non polar | 33892256 | Deoxycholic acid disulfate,2TMS,isomer #2 | C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C)[C@@]21C | 5505.2 | Standard polar | 33892256 | Deoxycholic acid disulfate,2TMS,isomer #3 | C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C)[C@@]21C | 4071.1 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,2TMS,isomer #3 | C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C)[C@@]21C | 4445.7 | Standard non polar | 33892256 | Deoxycholic acid disulfate,2TMS,isomer #3 | C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C)[C@@]21C | 5414.7 | Standard polar | 33892256 | Deoxycholic acid disulfate,3TMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C)[C@@]21C | 3993.5 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,3TMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C)[C@@]21C | 4642.7 | Standard non polar | 33892256 | Deoxycholic acid disulfate,3TMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C)[C@@]21C | 5259.2 | Standard polar | 33892256 | Deoxycholic acid disulfate,1TBDMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O)[C@@]21C | 4314.0 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,1TBDMS,isomer #2 | C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O)[C@@]21C | 4309.4 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,1TBDMS,isomer #3 | C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@@]21C | 4305.2 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,2TBDMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O)[C@@]21C | 4511.8 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,2TBDMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O)[C@@]21C | 5081.3 | Standard non polar | 33892256 | Deoxycholic acid disulfate,2TBDMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O)[C@@]21C | 5503.7 | Standard polar | 33892256 | Deoxycholic acid disulfate,2TBDMS,isomer #2 | C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@@]21C | 4505.7 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,2TBDMS,isomer #2 | C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@@]21C | 5061.7 | Standard non polar | 33892256 | Deoxycholic acid disulfate,2TBDMS,isomer #2 | C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@@]21C | 5548.2 | Standard polar | 33892256 | Deoxycholic acid disulfate,2TBDMS,isomer #3 | C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@@]21C | 4513.1 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,2TBDMS,isomer #3 | C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@@]21C | 5054.3 | Standard non polar | 33892256 | Deoxycholic acid disulfate,2TBDMS,isomer #3 | C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@@]21C | 5467.0 | Standard polar | 33892256 | Deoxycholic acid disulfate,3TBDMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@@]21C | 4677.5 | Semi standard non polar | 33892256 | Deoxycholic acid disulfate,3TBDMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@@]21C | 5515.9 | Standard non polar | 33892256 | Deoxycholic acid disulfate,3TBDMS,isomer #1 | C[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](OS(=O)(=O)O[Si](C)(C)C(C)(C)C)[C@@]21C | 5298.1 | Standard polar | 33892256 |
| Show more...
---|
Spectra |
---|
| GC-MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
---|
Predicted GC-MS | Predicted GC-MS Spectrum - Deoxycholic acid disulfate GC-MS (Non-derivatized) - 70eV, Positive | splash10-00bi-0221940000-ff9cb87c5327b9034a33 | 2017-09-01 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Deoxycholic acid disulfate GC-MS (1 TMS) - 70eV, Positive | splash10-0pi1-3241596000-46a811c469169aaf0722 | 2017-10-06 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Deoxycholic acid disulfate GC-MS ("Deoxycholic acid disulfate,1TMS,#1" TMS) - 70eV, Positive | Not Available | 2021-10-14 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Deoxycholic acid disulfate GC-MS (TMS_1_2) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Deoxycholic acid disulfate GC-MS (TMS_1_3) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Deoxycholic acid disulfate GC-MS (TBDMS_1_1) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Deoxycholic acid disulfate GC-MS (TBDMS_1_2) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Deoxycholic acid disulfate GC-MS (TBDMS_1_3) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum |
MS/MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
---|
Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Deoxycholic acid disulfate 10V, Negative-QTOF | splash10-0udi-0000490000-62117dcb59769336355c | 2017-09-01 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Deoxycholic acid disulfate 20V, Negative-QTOF | splash10-0fk9-1002910000-84791927b78d8249c364 | 2017-09-01 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Deoxycholic acid disulfate 40V, Negative-QTOF | splash10-0pc0-9003600000-fd8e2b31e9aaa7ec1deb | 2017-09-01 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Deoxycholic acid disulfate 10V, Negative-QTOF | splash10-0udi-0000090000-9cb46684f4638636bef9 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Deoxycholic acid disulfate 20V, Negative-QTOF | splash10-0udi-1000190000-37a540965cf22d2365c1 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Deoxycholic acid disulfate 40V, Negative-QTOF | splash10-0002-9000800000-748623a4eb6d359b8348 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Deoxycholic acid disulfate 10V, Positive-QTOF | splash10-000i-0000790000-80814aa48c365ac54e3b | 2017-09-01 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Deoxycholic acid disulfate 20V, Positive-QTOF | splash10-0a4i-0007900000-f3b0f1797f7869a2bebc | 2017-09-01 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Deoxycholic acid disulfate 40V, Positive-QTOF | splash10-001j-0309300000-299c2e6f63c974c25775 | 2017-09-01 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Deoxycholic acid disulfate 10V, Positive-QTOF | splash10-0udi-0103890000-01a42eecc4b3e8e1ac42 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Deoxycholic acid disulfate 20V, Positive-QTOF | splash10-0a4i-1009810000-5016a70a33bc838ad774 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Deoxycholic acid disulfate 40V, Positive-QTOF | splash10-0pb9-1209510000-db7d820c71b9172e131e | 2021-09-22 | Wishart Lab | View Spectrum |
| Show more...
---|
Biological Properties |
---|
Cellular Locations | |
---|
Biospecimen Locations | Not Available |
---|
Tissue Locations | Not Available |
---|
Pathways | |
---|
Normal Concentrations |
---|
| Not Available |
---|
Abnormal Concentrations |
---|
| Not Available |
---|
Associated Disorders and Diseases |
---|
Disease References | None |
---|
Associated OMIM IDs | None |
---|
External Links |
---|
DrugBank ID | Not Available |
---|
Phenol Explorer Compound ID | Not Available |
---|
FooDB ID | FDB022168 |
---|
KNApSAcK ID | Not Available |
---|
Chemspider ID | 402421 |
---|
KEGG Compound ID | Not Available |
---|
BioCyc ID | Not Available |
---|
BiGG ID | Not Available |
---|
Wikipedia Link | Not Available |
---|
METLIN ID | 5630 |
---|
PubChem Compound | 457190 |
---|
PDB ID | Not Available |
---|
ChEBI ID | 491276 |
---|
Food Biomarker Ontology | Not Available |
---|
VMH ID | Not Available |
---|
MarkerDB ID | Not Available |
---|
Good Scents ID | Not Available |
---|
References |
---|
Synthesis Reference | Bureeva, Svetlana; Andia-Pravdivy, Julian; Symon, Andrey; Bichucher, Anna; Moskaleva, Vera; Popenko, Vladimir; Shpak, Alexey; Shvets, Vitaly; Kozlov, Leonid; Kaplun, Alexander. Selective inhibition of the interaction of C1q with immunoglobulins and the classical pathway of complement activation by steroids and triterpenoids sulfates. Bioorganic & Medicinal Chemistry (2007), 15(10), 3489-3498. |
---|
Material Safety Data Sheet (MSDS) | Not Available |
---|
General References | - Hoffmann GF, Seppel CK, Holmes B, Mitchell L, Christen HJ, Hanefeld F, Rating D, Nyhan WL: Quantitative organic acid analysis in cerebrospinal fluid and plasma: reference values in a pediatric population. J Chromatogr. 1993 Jul 23;617(1):1-10. [PubMed:8376520 ]
|
---|