1.0 2010-04-08 22:10:51 UTC 2025-11-19 00:29:13 UTC FDB013685 Arnamiol From Armillaria mellea (honey mushroom). Arnamiol is found in mushrooms. Arnamiol C24H31ClO6 450.952 450.180916431 4-hydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1H,2H,4H,4aH,5H,6H,7H,7aH,7bH-cyclobuta[e]inden-2-yl 3-chloro-6-hydroxy-4-methoxy-2-methylbenzoate 4-hydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1H,2H,4H,4aH,5H,7H,7aH-cyclobuta[e]inden-2-yl 3-chloro-6-hydroxy-4-methoxy-2-methylbenzoate 102092-23-9 COC1=C(Cl)C(C)=C(C(=O)OC2CC3(C)C4CC(C)(C)CC4C(O)C(CO)=C23)C(O)=C1 InChI=1S/C24H31ClO6/c1-11-18(15(27)6-16(30-5)20(11)25)22(29)31-17-9-24(4)14-8-23(2,3)7-12(14)21(28)13(10-26)19(17)24/h6,12,14,17,21,26-28H,7-10H2,1-5H3 OMAGQTXDHXASNM-UHFFFAOYSA-N belongs to the class of organic compounds known as melleolides and analogues. Melleolides and analogues are compounds with a structure characterized by the presence of a 2-hydroxy-4-methoxy-6-methylbenzoic acid derivative linked to a 3,6,6,7b-tetramethyl-cyclobuta[e]indene moiety. Melleolides and analogues Organic compounds Lipids and lipid-like molecules Prenol lipids Sesquiterpenoids Aromatic homopolycyclic compounds 1-hydroxy-2-unsubstituted benzenoids 3-halobenzoic acids and derivatives Alkyl aryl ethers Anisoles Aryl chlorides Benzoyl derivatives Carboxylic acid esters Chlorobenzenes Hydrocarbon derivatives Meta cresols Methoxybenzenes Methoxyphenols Monocarboxylic acids and derivatives Organic oxides Organochlorides P-chlorophenols P-methoxybenzoic acids and derivatives Phenoxy compounds Primary alcohols Salicylic acid and derivatives Secondary alcohols Toluenes Vinylogous acids o-Hydroxybenzoic acid esters 1-hydroxy-2-unsubstituted benzenoid 3-halobenzoic acid or derivatives 4-chlorophenol 4-halophenol Alcohol Alkyl aryl ether Anisole Aromatic homopolycyclic compound Aryl chloride Aryl halide Benzenoid Benzoate ester Benzoic acid or derivatives Benzoyl Carboxylic acid derivative Carboxylic acid ester Chlorobenzene Ether Halobenzene Halobenzoic acid or derivatives Hydrocarbon derivative M-cresol Melleolide-skeleton Methoxybenzene Methoxyphenol Monocarboxylic acid or derivatives Monocyclic benzene moiety O-hydroxybenzoic acid ester Organic oxide Organic oxygen compound Organochloride Organohalogen compound Organooxygen compound P-methoxybenzoic acid or derivatives Phenol Phenol ether Phenoxy compound Primary alcohol Salicylic acid or derivatives Secondary alcohol Toluene Vinylogous acid logp 3.41 ALOGPS logs -4.90 ALOGPS solubility 5.66e-03 g/l ALOGPS melting_point Mp 132-134° logp 4.19 ChemAxon pka_strongest_acidic 9.32 ChemAxon pka_strongest_basic -2.8 ChemAxon iupac 4-hydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1H,2H,4H,4aH,5H,6H,7H,7aH,7bH-cyclobuta[e]inden-2-yl 3-chloro-6-hydroxy-4-methoxy-2-methylbenzoate ChemAxon average_mass 450.952 ChemAxon mono_mass 450.180916431 ChemAxon smiles COC1=C(Cl)C(C)=C(C(=O)OC2CC3(C)C4CC(C)(C)CC4C(O)C(CO)=C23)C(O)=C1 ChemAxon formula C24H31ClO6 ChemAxon inchi InChI=1S/C24H31ClO6/c1-11-18(15(27)6-16(30-5)20(11)25)22(29)31-17-9-24(4)14-8-23(2,3)7-12(14)21(28)13(10-26)19(17)24/h6,12,14,17,21,26-28H,7-10H2,1-5H3 ChemAxon inchikey OMAGQTXDHXASNM-UHFFFAOYSA-N ChemAxon polar_surface_area 96.22 ChemAxon refractivity 118.27 ChemAxon polarizability 48.81 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 5 ChemAxon donor_count 3 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 24899 Specdb::CMs 44167 Specdb::CMs 130763 Specdb::CMs 138497 Specdb::MsMs 54672 Specdb::MsMs 54673 Specdb::MsMs 54674 Specdb::MsMs 173727 Specdb::MsMs 173728 Specdb::MsMs 173729 Specdb::MsMs 2335504 Specdb::MsMs 2335505 Specdb::MsMs 2335506 Specdb::MsMs 2627228 Specdb::MsMs 2627229 Specdb::MsMs 2627230 HMDB35062 #<Reference:0x000055ce30cbc600> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322