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(Q83068885)
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English
2H-1-Benzopyran-2-one, 5,7-dimethoxy-6-(3-methyl-2-butenyl)-
chemical compound
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Statements
instance of
type of chemical entity
0 references
subclass of
biogenic coumarin
0 references
mass
274.120509056
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₁₆H₁₈O₄
0 references
canonical SMILES
O=C1OC2=CC(OC)=C(C(OC)=C2C=C1)CC=C(C)C
0 references
found in taxon
Toddalia asiatica
6 references
stated in
Cytotoxic coumarins from Toddalia asiatica
stated in
Chemical Constituents from the Root Bark of FormosanZanthoxylum Ailanthoides
stated in
Studies on the Chemical Constituents of Rutaceous Plants. LXVI. The Chemical Constituents of Toddalia asiatica (L.) LAM. (T. aculeata PERS.). (1). Chemical Constituents of the Root Bark
stated in
[Studies on the chemical constituents of rutaceous plants. LXVII. The chemical constituents of Toddalia asiatica (L.) Lam. (T. aculeata Pers). Examination of coumarins using supercritical fluid and soxhlet extraction. Is toddalolactone a genuine nat
stated in
Prenylated coumarins: natural phosphodiesterase-4 inhibitors from Toddalia asiatica
stated in
Toddaculin, a natural coumarin from Toddalia asiatica, induces differentiation and apoptosis in U-937 leukemic cells.
Zanthoxylum asiaticum
6 references
stated in
Chemical Constituents from the Root Bark of FormosanZanthoxylum Ailanthoides
stated in
Cytotoxic coumarins from Toddalia asiatica
stated in
Prenylated coumarins: natural phosphodiesterase-4 inhibitors from Toddalia asiatica
stated in
[Studies on the chemical constituents of rutaceous plants. LXVII. The chemical constituents of Toddalia asiatica (L.) Lam. (T. aculeata Pers). Examination of coumarins using supercritical fluid and soxhlet extraction. Is toddalolactone a genuine nat
stated in
Studies on the Chemical Constituents of Rutaceous Plants. LXVI. The Chemical Constituents of Toddalia asiatica (L.) LAM. (T. aculeata PERS.). (1). Chemical Constituents of the Root Bark
stated in
Toddaculin, a natural coumarin from Toddalia asiatica, induces differentiation and apoptosis in U-937 leukemic cells.
Identifiers
InChI
InChI=1S/C16H18O4/c1-10(2)5-6-11-13(18-3)9-14-12(16(11)19-4)7-8-15(17)20-14/h5,7-9H,6H2,1-4H3
0 references
InChIKey
KRQHZFHWEAJPNO-UHFFFAOYSA-N
0 references
CAS Registry Number
4335-12-0
1 reference
InChIKey
KRQHZFHWEAJPNO-UHFFFAOYSA-N
stated in
CAS Common Chemistry
retrieved
9 April 2021
reference URL
https://commonchemistry.cas.org/detail?cas_rn=4335-12-0
PubChem CID
5321960
1 reference
stated in
PubChem
retrieved
17 September 2022
based on heuristic
inferred from InChIKey
UniChem compound ID
33844702
1 reference
stated in
UniChem
DSSTox substance ID
DTXSID00195829
0 references
DSSTOX compound identifier
DTXCID90118320
0 references
Probes And Drugs ID
PD166759
0 references
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