Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H9NO2 |
Molecular Weight | 199.2054 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C2C=COC2=NC3=C1C=CC=C3
InChI
InChIKey=WIONIXOBNMDJFJ-UHFFFAOYSA-N
InChI=1S/C12H9NO2/c1-14-11-8-4-2-3-5-10(8)13-12-9(11)6-7-15-12/h2-7H,1H3
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: DNA Sources: https://www.ncbi.nlm.nih.gov/pubmed/7104872 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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PubMed
Title | Date | PubMed |
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Feeding deterrents from Dictamnus dasycarpus Turcz against two stored-product insects. | 2002 Mar 13 |
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A new prenylated arylnaphthalene lignan from Haplophyllum myrtifolium. | 2003 Sep |
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cis-Dihydrodiol, arene oxide and phenol metabolites of dictamnine: key intermediates in the biodegradation and biosynthesis of furoquinoline alkaloids. | 2005 Aug 21 |
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Furoquinoline alkaloids from the southern African Rutaceae Teclea natalensis. | 2005 Mar |
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Solar simulator-induced phototoxicity of the furoquinoline alkaloid dictamnine compared to 8-methoxypsoralen and 5-methoxypsoralen. | 2006 Aug |
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Pressurized liquid extraction followed by high-performance liquid chromatography for determination of seven active compounds in Cortex Dictamni. | 2006 Mar 10 |
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Isolation of secondary metabolites from Hortia oreadica (Rutaceae) leaves through high-speed counter-current chromatography. | 2009 May 8 |
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[Simultaneous determination of three active compounds in root barks of Dictamnus dasycarpus by RP-HPLC]. | 2010 Jan |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7104872
Curator's Comment: In vitro, labeled dictamnine was shown to form covalent monoadducts with purified DNA from M. hiemalis in the presence of long-wave ultraviolet light.
Unknown
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68085
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484-29-7
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HQZ3798D0A
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m4369
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DTXSID0041012
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SUBSTANCE RECORD