Lobaric acid结构式
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常用名 | Lobaric acid | 英文名 | Lobaric acid |
|---|---|---|---|---|
| CAS号 | 522-53-2 | 分子量 | 456.48500 | |
| 密度 | 1.265g/cm3 | 沸点 | 667.9ºC at 760mmHg | |
| 分子式 | C25H28O8 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 225.7ºC |
Lobaric acid用途Lobaric acid is a depsidone metabolite that has been isolated from Stereocaulon lichen species with antioxidant, antiproliferative, antiviral, and enzyme inhibitory activites. It scavenges superoxide radicals in a cell-free assay (IC50 = 97.9 μmol) and inhibits proliferation in a panel of leukemia, colorectal, gastric, breast, ovarian, prostate, pancreatic, and lung cancer cell lines (EC50s = 15.2-63.9 μg/ml). Lobaric acid inhibits protein tyrosine phosphatase 1B (PTP1B; IC50 = 0.87 μM for the human recombinant enzyme) and production of 12(S)-HETE (Item No. 34570) by 12(S)-lipoxygenase (IC50 = 28.5 μM). In vivo, lobaric acid (250 μM) decreases lesion number, but not lesion diameter, in tobacco leaves infected with tobacco mosaic virus (TMV). |
| 英文名 | 3-hydroxy-9-methoxy-6-oxo-7-pentanoyl-1-pentylbenzo[b][1,4]benzodioxepine-2-carboxylic acid |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.265g/cm3 |
|---|---|
| 沸点 | 667.9ºC at 760mmHg |
| 分子式 | C25H28O8 |
| 分子量 | 456.48500 |
| 闪点 | 225.7ºC |
| 精确质量 | 456.17800 |
| PSA | 119.36000 |
| LogP | 5.52950 |
| InChIKey | JHEWMLHQNRHTQX-UHFFFAOYSA-N |
| SMILES | CCCCCc1c2c(cc(O)c1C(=O)O)OC(=O)c1c(cc(OC)cc1C(=O)CCCC)O2 |
| 折射率 | 1.579 |
| 储存条件 | -20°C,密闭,干燥 |
| Lobaric acid上游产品 0 | |
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| Lobaric acid下游产品 2 | |
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实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
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实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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实验名称:ERK5 transcriptional activity HTS
来源:24565
靶标:N/A
External Id:ERK5 transcriptional activity-HTS
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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实验名称:Inhibition of PTP1B (1 to 298 residues) (unknown origin) using p-nitrophenylphosphate...
来源:ChEMBL
靶标:Tyrosine-protein phosphatase non-receptor type 1
External Id:CHEMBL4150189
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实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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实验名称:Confirmed inhibitors of the Choline Transporter (CHT)
来源:1043
靶标:high affinity choline transporter 1 [Homo sapiens]
External Id:SAID_488997
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| Usnetic acid |
| Lobaric acid |