Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q63396516)
Watch
English
amorphigenin
chemical compound
In more languages
edit
Statements
instance of
type of chemical entity
0 references
subclass of
8'-Hydroxyrotenone
1 reference
based on heuristic
inferred from SMILES
mass
410.136553044
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₂₃H₂₂O₇
0 references
canonical SMILES
O=C1C2=CC=C3OC(C(=C)CO)CC3=C2OC4COC5=CC(OC)=C(OC)C=C5C14
0 references
isomeric SMILES
COC1=C(C=C2C(=C1)[C@H]3[C@@H](CO2)OC4=C(C3=O)C=CC5=C4C[C@@H](O5)C(=C)CO)OC
0 references
found in taxon
Berchemia discolor
2 references
stated in
Prenylated flavonoids from the root bark of Berchemia discolor, a Tanzanian medicinal plant
stated in
Prenylated Flavonoids from the Root Bark of Berchemia discolor, a Tanzanian Medicinal Plant
Amorpha fruticosa
8 references
stated in
Antitumor agents, 138. Rotenoids and isoflavones as cytotoxic constitutents from Amorpha fruticosa.
stated in
Structural Elucidation and Chemical Conversion of Amorphispironone, a Novel Spironone from Amorpha fruticosa, to Rotenoids.
stated in
Pre-isoflavonoid stages in the biosynthesis of amorphigenin: ring-D formation and ring-A migration
stated in
Enzymic oxidative modification of prenyl groups. The biosynthetic origins of the E-ring systems of rotenone and amorphigenin
stated in
Biosynthesis of the A/B/C/D-ring system of the rotenoid amorphigenin by Amorpha fruticosa seedlings
stated in
Biosynthesis of rotenone and amorphigenin. Study of the origins of isopropenyl-substituted dihydrofuran E-rings using isotopically labelled late precursors
stated in
Studies on inhibitors of skin tumor promotion, XII. Rotenoids from Amorpha fruticosa.
stated in
Biosynthesis of rotenoids by Amorpha fruticosa: sequence, specificity, and stereochemistry in the development of the hemiterpenoid segment
Dalbergia monetaria
2 references
stated in
Isoflavanoid constituents from Dalbergia monetaria
stated in
Isoflavanoid constituents from Dalbergia monetaria
Dalbergia ovalis
1 reference
stated in
Isoflavanoid constituents from Dalbergia monetaria
Identifiers
InChI
InChI=1S/C23H22O7/c1-11(9-24)16-7-14-15(29-16)5-4-12-22(25)21-13-6-18(26-2)19(27-3)8-17(13)28-10-20(21)30-23(12)14/h4-6,8,16,20-21,24H,1,7,9-10H2,2-3H3/t16-,20-,21+/m1/s1
0 references
InChIKey
ZJMLELXRQUXRIU-HBGVWJBISA-N
0 references
CAS Registry Number
4208-09-7
1 reference
InChIKey
ZJMLELXRQUXRIU-HBGVWJBISA-N
stated in
CAS Common Chemistry
retrieved
9 April 2021
reference URL
https://commonchemistry.cas.org/detail?cas_rn=4208-09-7
PubChem CID
92207
1 reference
matched by identifier from
InChIKey
InChIKey
ZJMLELXRQUXRIU-HBGVWJBISA-N
ChEBI ID
183897
mapping relation type
exact match
2 references
stated in
ChEBI release 2022-06-13
matched by identifier from
International Chemical Identifier
InChI
InChI=1S/C23H22O7/c1-11(9-24)16-7-14-15(29-16)5-4-12-22(25)21-13-6-18(26-2)19(27-3)8-17(13)28-10-20(21)30-23(12)14/h4-6,8,16,20-21,24H,1,7,9-10H2,2-3H3/t16-,20-,21+/m1/s1
UniChem compound ID
407691
1 reference
stated in
UniChem
MassBank accession ID
MSBNK-Washington_State_Univ-BML00164
0 references
MSBNK-Washington_State_Univ-BML00178
0 references
MSBNK-Washington_State_Univ-BML00192
0 references
MSBNK-Washington_State_Univ-BML00205
0 references
MSBNK-Washington_State_Univ-BML00218
0 references
MSBNK-Washington_State_Univ-BML00231
0 references
MSBNK-Washington_State_Univ-BML80730
0 references
MSBNK-Washington_State_Univ-BML80731
0 references
MSBNK-Washington_State_Univ-BML80732
0 references
MSBNK-Washington_State_Univ-BML80733
0 references
DSSTox substance ID
DTXSID70962267
1 reference
matched by identifier from
InChIKey
InChIKey
ZJMLELXRQUXRIU-HBGVWJBISA-N
DSSTOX compound identifier
DTXCID201390078
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
