Tetronasin (CHEM027691)
| Record Information | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Version | 1.0 | ||||||||
| Creation Date | 2016-05-25 23:54:52 UTC | ||||||||
| Update Date | 2026-05-14 20:34:46 UTC | ||||||||
| Accession Number | CHEM027691 | ||||||||
| Identification | |||||||||
| Common Name | Tetronasin | ||||||||
| Class | Small Molecule | ||||||||
| Description | Tetronasin is an organic compound with the chemical formula C35H54O8. Tetronasin belongs to the terpene glycosides, a subclass of prenol lipids within the organic compounds. With an average molecular weight of 602.81 g/mol, Tetronasin is a heavy molecule. This compound is found in or released from one recorded source: healthcare, pharmaceuticals & veterinary products (antibiotics). Recorded exposure routes for this substance include inhalation and oral administration. | ||||||||
| Contaminant Sources |
| ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C35H54O8 | ||||||||
| Average Molecular Mass | 602.809 g/mol | ||||||||
| Monoisotopic Mass | 602.382 g/mol | ||||||||
| CAS Registry Number | 75139-06-9 | ||||||||
| IUPAC Name | Not Available | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | [H][C@@]1(C[C@H](C)[C@@]([H])(O1)[C@@H](C)\C=C\[C@@H]1CC[C@@H](C)[C@@H](O1)C(\CO)=C\[C@H]1CCC[C@@H](C)[C@]1([H])[C@H](C)C(=O)C1=C(O)COC1=O)[C@H](C)OC | ||||||||
| InChI Identifier | InChI=1S/C35H54O8/c1-19-9-8-10-25(30(19)23(5)32(38)31-28(37)18-41-35(31)39)16-26(17-36)34-21(3)12-14-27(42-34)13-11-20(2)33-22(4)15-29(43-33)24(6)40-7/h11,13,16,19-25,27,29-30,33-34,36-37H,8-10,12,14-15,17-18H2,1-7H3/b13-11+,26-16+/t19-,20+,21-,22+,23+,24+,25-,27-,29+,30+,33-,34-/m1/s1 | ||||||||
| InChI Key | BJUFZCRLMQPLMO-RHKPWOOXSA-N | ||||||||
| Chemical Taxonomy | |||||||||
| Classification | Not classified | ||||||||
| Biological Properties | |||||||||
| Status | Detected and Not Quantified | ||||||||
| Origin | Not Available | ||||||||
| Cellular Locations | Not Available | ||||||||
| Biofluid Locations | Not Available | ||||||||
| Tissue Locations | Not Available | ||||||||
| Pathways | Not Available | ||||||||
| Applications | Not Available | ||||||||
| Biological Roles | Not Available | ||||||||
| Chemical Roles | Not Available | ||||||||
| Physical Properties | |||||||||
| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
| ||||||||
| Predicted Properties | Not Available | ||||||||
| Spectra | |||||||||
| Spectra | Not Available | ||||||||
| Toxicity Profile | |||||||||
| Route of Exposure | Not Available | ||||||||
| Mechanism of Toxicity | Not Available | ||||||||
| Metabolism | Not Available | ||||||||
| Toxicity Values | Not Available | ||||||||
| Lethal Dose | Not Available | ||||||||
| Carcinogenicity (IARC Classification) | Not Available | ||||||||
| Uses/Sources | Not Available | ||||||||
| Minimum Risk Level | Not Available | ||||||||
| Health Effects | Not Available | ||||||||
| Symptoms | Not Available | ||||||||
| Treatment | Not Available | ||||||||
| Concentrations | |||||||||
| Not Available | |||||||||
| External Links | |||||||||
| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
