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(Q104375869)
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Squamatic acid
chemical compound
Squamatsaure
iso-squamatic acid
sphaerophoric acid
uncinatic acid
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Statements
instance of
type of chemical entity
0 references
subclass of
depside
0 references
mass
390.095082156
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₁₉H₁₈O₉
0 references
canonical SMILES
O=C(O)C=1C(O)=C(C(=O)OC=2C=C(C(C(=O)O)=C(O)C2C)C)C(=CC1OC)C
0 references
found in taxon
Loxospora ochrophaea
1 reference
stated in
Two New Lichen Products, Elatinic Acid and Methyl Barbatate, from the Genus Haematomma (Ascomycotina, Haematommataceae)
Siphula applanata
1 reference
stated in
Chemical Studies on Lichens. 6. The Chemistry of the Genus Siphula. II.
Siphula polyschides
1 reference
stated in
Chemical Studies on Lichens. 6. The Chemistry of the Genus Siphula. II.
Siphula subulata
1 reference
stated in
Chemical Studies on Lichens. 6. The Chemistry of the Genus Siphula. II.
Cladonia incrassata
1 reference
stated in
Uncommon Chlorinated Xanthone and Other Antibacterial Compounds from the Lichen Cladonia incrassata
Lethariella cladonioides
1 reference
stated in
Characterisation of phenols and antioxidant and hypolipidaemic activities of Lethariella cladonioides
Flavocetraria cucullata
1 reference
stated in
Lichen secondary metabolites in Flavocetraria cucullata exhibit anti-cancer effects on human cancer cells through the induction of apoptosis and suppression of tumorigenic potentials
Cladonia uncialis
1 reference
stated in
Lichen Depsides and Tridepsides: Progress in Pharmacological Approaches
Thamnolia vermicularis
2 references
stated in
β-Orcinol-type depsides from the lichen Thamnolia vermicularis.
stated in
Lichen Depsides and Tridepsides: Progress in Pharmacological Approaches
Nephromopsis cucullata
1 reference
stated in
Lichen secondary metabolites in Flavocetraria cucullata exhibit anti-cancer effects on human cancer cells through the induction of apoptosis and suppression of tumorigenic potentials
subject has role
antineoplastic
5 references
stated in
Molecular and Cellular Biology
retrieved
7 September 2022
DOI
10.1007/s11010-017-3178-7
stated in
Planta Medica
DOI
10.1055/s-0031-1280096
retrieved
7 September 2022
stated in
Cells
DOI
10.3390/cells11071084
retrieved
7 September 2022
stated in
PLOS One
DOI
10.1371/journal.pone.0111575
retrieved
7 September 2022
stated in
Lichen Depsides and Tridepsides: Progress in Pharmacological Approaches
antimicrobial agent
4 references
stated in
Natural Product Research
retrieved
7 September 2022
DOI
10.1080/14786419.2015.1005616
DOI
10.18388/abp.2019_2891
retrieved
7 September 2022
stated in
Planta Medica
retrieved
7 September 2022
DOI
10.1055/s-0034-1382827
stated in
Lichen Depsides and Tridepsides: Progress in Pharmacological Approaches
antifungal
1 reference
DOI
10.18388/abp.2019_2891
retrieved
7 September 2022
Identifiers
InChI
InChI=1S/C19H18O9/c1-7-5-10(9(3)15(20)12(7)17(22)23)28-19(26)13-8(2)6-11(27-4)14(16(13)21)18(24)25/h5-6,20-21H,1-4H3,(H,22,23)(H,24,25)
0 references
InChIKey
WCWYEXBIRSSVGF-UHFFFAOYSA-N
0 references
PubChem CID
5321482
2 references
stated in
PubChem
retrieved
17 September 2022
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
WCWYEXBIRSSVGF-UHFFFAOYSA-N
ChEBI ID
144231
mapping relation type
exact match
2 references
stated in
ChEBI release 2021-03-01
matched by identifier from
International Chemical Identifier
InChI
InChI=1S/C19H18O9/c1-7-5-10(9(3)15(20)12(7)17(22)23)28-19(26)13-8(2)6-11(27-4)14(16(13)21)18(24)25/h5-6,20-21H,1-4H3,(H,22,23)(H,24,25)
UniChem compound ID
1022069
1 reference
stated in
UniChem
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