# dhurrin

> chemical compound

**Wikidata**: [Q908811](https://www.wikidata.org/wiki/Q908811)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Dhurrin)  
**Source**: https://4ort.xyz/entity/dhurrin


## References

1. dhurrin. Global Substance Registration System
2. [CAS Common Chemistry](https://commonchemistry.cas.org/detail?cas_rn=499-20-7)
3. Dhurrin. PubChem
4. ChEBI release 2020-09-01
5. Gene Ontology release 2019-11-16
6. Gene Ontology release 2020-05-02
7. Dhurrin. ChemSpider
8. (S)-4-hydroxymandelonitrile beta-D-glucoside. ChEBI
9. Dhurrin-6'-glucoside, a cyanogenic diglucoside from Sorghum bicolor
10. Dhurrin synthesis in sorghum is regulated at the transcriptional level and induced by nitrogen fertilization in older plants
11. Tissue Distributions of Dhurrin and of Enzymes Involved in Its Metabolism in Leaves of Sorghum bicolor
12. Leakage of Dhurrin and p-Hydroxybenzaldehyde from Young Sorghum Shoots Immersed in Various Solvents
13. Biosynthesis of the Cyanogenic Glucoside Dhurrin in Seedlings of Sorghum bicolor (L.) Moench and Partial Purification of the Enzyme System Involved
14. Turnover of dhurrin in green sorghum seedlings
15. The primary sequence of cytochrome P450tyr, the multifunctional N-hydroxylase catalyzing the conversion of L-tyrosine to p-hydroxyphenylacetaldehyde oxime in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench
16. 2-nitro-3-(p-hydroxyphenyl)propionate and aci-1-nitro-2-(p-hydroxyphenyl)ethane, two intermediates in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench.
17. Cytochrome P-450TYR is a multifunctional heme-thiolate enzyme catalyzing the conversion of L-tyrosine to p-hydroxyphenylacetaldehyde oxime in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench
18. The UDP-glucose:p-hydroxymandelonitrile-O-glucosyltransferase that catalyzes the last step in synthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor. Isolation, cloning, heterologous expression, and substrate specificity.
19. The biosynthesis of cyanogenic glucosides in higher plants. Identification of three hydroxylation steps in the biosynthesis of dhurrin in Sorghum bicolor (L.) Moench and the involvement of 1-ACI-nitro-2-(p-hydroxyphenyl)ethane as an intermediate.
20. Dhurrin, the cyanogenic glucoside of Cercocarpus ledifolius
21. Biological activity of dhurrin and other compounds from Johnson grass (Sorghum halepense)
22. Dhurrin, (−)-catechin, flavonol glycosides and flavones from Chamaebatia foliolosa
23. 4-Hydroxymandelonitrile glucosides, dhurrin in Suckleya suckleyana and taxiphyllin in Girgensohnia oppositiflora (Chenopodiaceae)
24. Über die Cyanogenese vonBambusa vulgaris undB. guadua
25. Phenolic dimers and an indole alkaloid from Campylospermum flavum (Ochnaceae).
26. Cyanogenic glycosides and menisdaurin from Guazuma ulmifolia, Ostrya virgininana, Tiquilia plicata and Tiquilia canescens
27. Taxiphyllin from Henriettella fascicularis
28. The absolute stereostructures of cyanogenic glycosides, hydracyanosides A, B, and C, from the leaves and stems of Hydrangea macrophylla
29. New Cyanoglycosides, Hydracyanosides D, E, and F, from the Leaves of Hydrangea macrophylla
30. Dhurrin and p-hydroxybenzaldehyde in seedlings of various Sorghum species
31. Phytochemical constituents from Salsola tetrandra.
32. Cyanogenesis in the proteaceae
33. (S)-(β-D-glucopyranosyloxy)(4-hydroxyphenyl)acetonitrile. ECHA Substance Infocard database
34. Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
35. UniChem