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(Q76416414)
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Conocarpan
chemical compound
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Statements
instance of
type of chemical entity
0 references
subclass of
4-(3-Methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl)phenol
1 reference
based on heuristic
inferred from SMILES
mass
266.130679816
dalton
1 reference
based on heuristic
inferred from SMILES
stereoisomer of
(-)-epi-Conocarpan
1 reference
based on heuristic
inferred from InChI
(+)-conocarpan
1 reference
based on heuristic
inferred from InChI
chemical formula
C₁₈H₁₈O₂
0 references
canonical SMILES
OC1=CC=C(C=C1)C2OC3=CC=C(C=CC)C=C3C2C
0 references
isomeric SMILES
C/C=C/C1=CC2=C(C=C1)O[C@H]([C@@H]2C)C3=CC=C(C=C3)O
0 references
found in taxon
Krameria lanceolata
1 reference
stated in
Neolignans and nor-neolignans from Krameria lanceolata
Piper regnellii
4 references
stated in
Neolignanas e análise do óleo essencial das folhas de Piper regnellii (Miq.) C. DC. var. pallescens (C. DC.) Yunck
stated in
Antifungal principles from Piper fulvescens.
stated in
Phenylpropanoids and neolignans from Piper regnellii
stated in
Activity of neolignans isolated from Piper regnellii (MIQ.) C. DC. var. pallescens (C. DC.) YUNCK against Trypanosoma cruzi
Krameria paucifolia
1 reference
stated in
Neolignans and nor-neolignans from Krameria paucifolia
Krameria tomentosa
2 references
stated in
Complete assignment of the1H and13C NMR spectra of four triterpenes of the ursane, artane, lupane and friedelane groups
stated in
Krametosan, a new trinorlignan from the roots of Krameria tomentosa
Anogeissus acuminata
1 reference
stated in
Revision of the NMR Assignments of Pterostilbene and of Dihydrodehydrodiconieferyl alcohol: Cytotoxic Constituents fromAnogeissus acuminata
Krameria cytisoides
1 reference
stated in
Lignans neolignans and norneolignans from krameria cystisoides
Krameria erecta
2 references
stated in
Lignans and neolignans from Krameria parvifolia
stated in
Lignans and nor-neolignans from Krameria interior
Krameria sonorae
2 references
stated in
Neolignans, Norneolignans, and Other Components from Krameria sonorae1
stated in
Hermosillol, an 8,3′-neolignan from Krameria sonorae
Krameria lappacea
2 references
stated in
ChemInform Abstract: Isolation and Structure Determination of New Active Neolignans and Norneolignans from Ratanhia.
stated in
Lignan derivatives from Krameria lappacea roots inhibit acute inflammation in vivo and pro-inflammatory mediators in vitro
Piper aequale
1 reference
stated in
Neolignans from Piper aequale
Piper decurrens
1 reference
stated in
Insecticidal neolignans from Piper decurrens
Caryodaphnopsis baviensis
1 reference
stated in
Neolignans from Caryodaphnopsis baviensis
Piper solmsianum
1 reference
stated in
Evaluation of antifungal activity of Piper solmsianum C. DC. var. solmsianum (Piperaceae).
Terminalia phillyreifolia
1 reference
stated in
Revision of the NMR Assignments of Pterostilbene and of Dihydrodehydrodiconieferyl alcohol: Cytotoxic Constituents fromAnogeissus acuminata
Krameria grayi
2 references
stated in
Neolignans, Norneolignans, and Other Components from Krameria sonorae1
stated in
Hermosillol, an 8,3′-neolignan from Krameria sonorae
Krameria bicolor
2 references
stated in
Neolignans, Norneolignans, and Other Components from Krameria sonorae1
stated in
Hermosillol, an 8,3′-neolignan from Krameria sonorae
Identifiers
InChI
InChI=1S/C18H18O2/c1-3-4-13-5-10-17-16(11-13)12(2)18(20-17)14-6-8-15(19)9-7-14/h3-12,18-19H,1-2H3/b4-3+/t12-,18-/m1/s1
0 references
InChIKey
GXJSAHXNLJFDPO-CGBXWHSCSA-N
0 references
CAS Registry Number
56319-02-9
0 references
PubChem CID
10999992
1 reference
matched by identifier from
InChIKey
InChIKey
GXJSAHXNLJFDPO-CGBXWHSCSA-N
UniChem compound ID
9688860
1 reference
stated in
UniChem
DSSTox substance ID
DTXSID70451404
2 references
stated in
Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
matched by identifier from
InChIKey
InChIKey
GXJSAHXNLJFDPO-CGBXWHSCSA-N
DSSTOX compound identifier
DTXCID60402223
0 references
NSC number
727405
0 references
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