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(Q105025208)
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deidaclin
chemical compound
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Statements
instance of
type of chemical entity
0 references
subclass of
Tetraphyllin A
1 reference
based on heuristic
inferred from SMILES
1-(Hexopyranosyloxy)cyclopent-2-ene-1-carbonitrile
1 reference
based on heuristic
inferred from SMILES
mass
271.105587264
dalton
1 reference
based on heuristic
inferred from SMILES
stereoisomer of
Deidaclin
1 reference
based on heuristic
inferred from InChI
chemical formula
C₁₂H₁₇NO₆
0 references
canonical SMILES
N#CC1(OC2OC(CO)C(O)C(O)C2O)C=CCC1
0 references
isomeric SMILES
N#C[C@@]1(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=CCC1
0 references
found in taxon
Passiflora coriacea
1 reference
stated in
Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts
Passiflora foetida
2 references
stated in
Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts
stated in
Cyanogenesis of Passiflora foetida
Passiflora herbertiana
1 reference
stated in
Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts
Passiflora suberosa
2 references
stated in
Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts
stated in
Structure determination of natural epoxycyclopentanes by x-ray crystallography and NMR spectroscopy
Passiflora tetrandra
2 references
stated in
Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts
stated in
Tetraphyllins A and B, deidaclin and epitetraphyllin B from Tetrapathaea tetrandra (Passifloraceae)
Turnera ulmifolia
3 references
stated in
Biosynthesis of cyanohydrin glucosides from unnatural nitriles in intact tissue of Passiflora morifolia and Turnera angustifolia
stated in
Deidaclin from turnera ulmifolia
stated in
Cyclopentenylglycine, a precursor of deidaclin in Turnera ulmifolia
Malesherbia ardens
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia angustisecta
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia arequipensis
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia auristipulata
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia deserticola
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia fasciculata
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia humilis
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia lactea
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia lanceolata
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia linearifolia
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia lirana
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia multiflora
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia obtusa
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia paniculata
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia tenuifolia
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia scarlatiflora
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia splendens
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia tubulosa
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Adenia globosa
1 reference
stated in
Deidaclin and Tetraphyllin A, Epimeric Glucosides of 2-Cyclopentenone Cyanohydrin, in Adenia globosa ssp. globosa Engl. (Passifloraceae). Crystal Structure of Deidaclin Tetraacetate.
Kiggelaria africana
1 reference
stated in
Structure determination of natural epoxycyclopentanes by x-ray crystallography and NMR spectroscopy
Malesherbia humilis var. propinqua
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia lirana var. bracteata
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Malesherbia lirana var. subglabrifolia
1 reference
stated in
Cyanogenic glycosides of Malesherbia
Identifiers
InChI
InChI=1S/C12H17NO6/c13-6-12(3-1-2-4-12)19-11-10(17)9(16)8(15)7(5-14)18-11/h1,3,7-11,14-17H,2,4-5H2/t7-,8-,9+,10-,11+,12-/m1/s1
0 references
InChIKey
HBCFZAXOSTUEHA-XZPZHEHLSA-N
0 references
PubChem CID
15596187
2 references
stated in
PubChem
retrieved
17 September 2022
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
HBCFZAXOSTUEHA-XZPZHEHLSA-N
UniChem compound ID
97406918
1 reference
stated in
UniChem
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