Trichodesmine
Modify Date: 2026-08-04 08:15:32
Trichodesmine structure
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Common Name | Trichodesmine | ||
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| CAS Number | 548-90-3 | Molecular Weight | 353.4 | |
| Density | 1.29g/cm3 | Boiling Point | 546.5ºC at 760 mmHg | |
| Molecular Formula | C18H27NO6 | Melting Point | 160-161 °C | |
| MSDS | N/A | Flash Point | 284.3ºC | |
Use of TrichodesmineTrichodesmine is a dehydropyrrolizidine alkaloid. Trichodesmine can produces hepatotoxicty, pneumo- and neurotoxicity in vivo[1][2]. |
| Name | 2-chloro-4-(4-chlorophenyl)phenol |
|---|---|
| Synonym | More Synonyms |
| Description | Trichodesmine is a dehydropyrrolizidine alkaloid. Trichodesmine can produces hepatotoxicty, pneumo- and neurotoxicity in vivo[1][2]. |
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| Related Catalog | |
| In Vitro | Trichodesmine produces pulmonary and hepatic lesions in donkeys[2]. |
| References |
| Density | 1.29g/cm3 |
|---|---|
| Boiling Point | 546.5ºC at 760 mmHg |
| Melting Point | 160-161 °C |
| Molecular Formula | C18H27NO6 |
| Molecular Weight | 353.4 |
| Flash Point | 284.3ºC |
| Exact Mass | 353.18383758 |
| PSA | 20.23000 |
| LogP | 4.36600 |
| Index of Refraction | 1.571 |
| InChIKey | SOODLZHDDSGRKL-FOOXYVKASA-N |
| SMILES | CC(C)[C@H]1C(=O)O[C@@H]2CCN3[C@@H]2C(=CC3)COC(=O)[C@]([C@]1(C)O)(C)O |
| RIDADR | UN 1544 |
|---|---|
| Packaging Group | III |
| Hazard Class | 6.1(b) |
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Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
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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: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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Name: USP8 deubiquitinase inhibition: Primary qHTS
Source: 24642
Target: ubiquitin specific peptidase 8
External Id: USP8 FAST DUB HTS Primary
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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: USP17 deubiquitinase inhibition: Primary qHTS
Source: 24642
Target: ubiquitin specific peptidase 17 like family member 5
External Id: USP17 FAST DUB HTS Primary
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Name: USP7 deubiquitinase inhibition: Primary qHTS
Source: 24642
Target: ubiquitin specific peptidase 7
External Id: USP7 FAST DUB HTS Primary
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Name: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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| 3,4'-Dichloro-4-biphenylol |
| Trichodesmine |
| [1,1'-Biphenyl]-4-ol,3,4'-dichloro |