NCBI Taxonomy: 306512

Aglaia perviridis (ncbi_taxid: 306512)

found 51 associated metabolites at species taxonomy rank level.

Ancestor: Aglaia

Child Taxonomies: none taxonomy data.

Scopoletin

7-hydroxy-6-methoxy-2H-chromen-2-one

C10H8O4 (192.0423)


Scopoletin is a hydroxycoumarin that is umbelliferone bearing a methoxy substituent at position 6. It has a role as a plant growth regulator and a plant metabolite. It is functionally related to an umbelliferone. Scopoletin is a natural product found in Ficus auriculata, Haplophyllum cappadocicum, and other organisms with data available. Scopoletin is a coumarin compound found in several plants including those in the genus Scopolia and the genus Brunfelsia, as well as chicory (Cichorium), redstem wormwood (Artemisia scoparia), stinging nettle (Urtica dioica), passion flower (Passiflora), noni (Morinda citrifolia fruit) and European black nightshade (Solanum nigrum) that is comprised of umbelliferone with a methoxy group substituent at position 6. Scopoletin is used to standardize and establish pharmacokinetic properties for products derived from the plants that produce it, such as noni extract. Although the mechanism(s) of action have not yet been established, this agent has potential antineoplastic, antidopaminergic, antioxidant, anti-inflammatory and anticholinesterase effects. Plant growth factor derived from the root of Scopolia carniolica or Scopolia japonica. See also: Arnica montana Flower (part of); Lycium barbarum fruit (part of); Viburnum opulus root (part of). Isolated from Angelica acutiloba (Dong Dang Gui). Scopoletin is found in many foods, some of which are lambsquarters, lemon, sunflower, and sherry. Scopoletin is found in anise. Scopoletin is isolated from Angelica acutiloba (Dong Dang Gui A hydroxycoumarin that is umbelliferone bearing a methoxy substituent at position 6. Acquisition and generation of the data is financially supported in part by CREST/JST. [Raw Data] CBA72_Scopoletin_pos_20eV.txt [Raw Data] CBA72_Scopoletin_pos_40eV.txt [Raw Data] CBA72_Scopoletin_neg_30eV.txt [Raw Data] CBA72_Scopoletin_neg_50eV.txt [Raw Data] CBA72_Scopoletin_pos_50eV.txt [Raw Data] CBA72_Scopoletin_pos_10eV.txt [Raw Data] CBA72_Scopoletin_neg_40eV.txt [Raw Data] CBA72_Scopoletin_neg_10eV.txt [Raw Data] CBA72_Scopoletin_pos_30eV.txt [Raw Data] CBA72_Scopoletin_neg_20eV.txt Scopoletin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=92-61-5 (retrieved 2024-07-12) (CAS RN: 92-61-5). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Scopoletin is an inhibitor of acetylcholinesterase (AChE). Scopoletin is an inhibitor of acetylcholinesterase (AChE).

   

Piperine

(2E,4E)-5-(2H-1,3-benzodioxol-5-yl)-1-(piperidin-1-yl)penta-2,4-dien-1-one

C17H19NO3 (285.1365)


Piperine, also known as fema 2909, belongs to the class of organic compounds known as alkaloids and derivatives. These are naturally occurring chemical compounds that contain mostly basic nitrogen atoms. This group also includes some related compounds with neutral and even weakly acidic properties. Also some synthetic compounds of similar structure are attributed to alkaloids. In addition to carbon, hydrogen and nitrogen, alkaloids may also contain oxygen, sulfur and more rarely other elements such as chlorine, bromine, and phosphorus. Piperine is a pepper tasting compound. Piperine is found in the highest concentration within pepper (Piper nigrum) and many other Piper species. Piperine has also been detected, but not quantified, in dills and herbs and spices. Piperine is responsible for the hot taste of pepper. Piperine has been used in trials studying the treatment of Multiple Myeloma and Deglutition Disorders. It is used to impart pungent taste to brandy. Piperine is a N-acylpiperidine that is piperidine substituted by a (1E,3E)-1-(1,3-benzodioxol-5-yl)-5-oxopenta-1,3-dien-5-yl group at the nitrogen atom. It is an alkaloid isolated from the plant Piper nigrum. It has a role as a NF-kappaB inhibitor, a plant metabolite, a food component and a human blood serum metabolite. It is a member of benzodioxoles, a N-acylpiperidine, a piperidine alkaloid and a tertiary carboxamide. It is functionally related to an (E,E)-piperic acid. Bioperine has been used in trials studying the treatment of Multiple Myeloma and Deglutition Disorders. Piperine is a natural product found in Macropiper, Piper boehmeriifolium, and other organisms with data available. See also: Black Pepper (part of) ... View More ... Constituent of pepper (Piper nigrum) and many other Piper subspecies (Piperaceae). It is used to impart pungent taste to brandy. Responsible for the hot taste of pepper. Flavour ingredient. Piperine is found in dill, herbs and spices, and pepper (spice). A N-acylpiperidine that is piperidine substituted by a (1E,3E)-1-(1,3-benzodioxol-5-yl)-5-oxopenta-1,3-dien-5-yl group at the nitrogen atom. It is an alkaloid isolated from the plant Piper nigrum. Piperine. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=94-62-2 (retrieved 2024-07-01) (CAS RN: 94-62-2). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Piperine, a natural alkaloid isolated from Piper nigrum L, inhibits P-glycoprotein and CYP3A4 activities with an IC50 value of 61.94±0.054 μg/mL in HeLa cell. Piperine, a natural alkaloid isolated from Piper nigrum L, inhibits P-glycoprotein and CYP3A4 activities with an IC50 value of 61.94±0.054 μg/mL in HeLa cell.

   

5-(1,3-Benzodioxol-5-yl)-1-piperidin-1-ylpenta-2,4-dien-1-one

5-(2H-1,3-benzodioxol-5-yl)-1-(piperidin-1-yl)penta-2,4-dien-1-one

C17H19NO3 (285.1365)


   

Eichlerianic acid

3-[(3S,3aR,5aR,6S,7S,9aR,9bR)-3-[(2S,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid

C30H50O4 (474.3709)


Eichlerianic acid is a diterpene glycoside. It has a role as a metabolite. Eichlerianic acid is a natural product found in Aglaia foveolata, Aglaia rubiginosa, and other organisms with data available. A natural product found in Aglaia foveolata.

   

Piperine

Isopiperine

C17H19NO3 (285.1365)


Constituent of pepper (Piper nigrum) (Piperaceae). Isopiperine is found in herbs and spices and pepper (spice). C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic Origin: Plant; SubCategory_DNP: Alkaloids derived from lysine, Piperidine alkaloids D004791 - Enzyme Inhibitors > D065607 - Cytochrome P-450 Enzyme Inhibitors Annotation level-1 MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; MXXWOMGUGJBKIW-YPCIICBESA-N_STSL_0203_Piperine_0031fmol_180831_S2_L02M02_45; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. relative retention time with respect to 9-anthracene Carboxylic Acid is 1.245 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.243 Piperine, a natural alkaloid isolated from Piper nigrum L, inhibits P-glycoprotein and CYP3A4 activities with an IC50 value of 61.94±0.054 μg/mL in HeLa cell. Piperine, a natural alkaloid isolated from Piper nigrum L, inhibits P-glycoprotein and CYP3A4 activities with an IC50 value of 61.94±0.054 μg/mL in HeLa cell.

   

cabraleahydroxylactone

cabraleahydroxylactone

C27H44O3 (416.329)


A tetracyclic triterpenoid isolated from the stems of Aglaia abbreviata.

   

Scopoletin

Scopoletin

C10H8O4 (192.0423)


relative retention time with respect to 9-anthracene Carboxylic Acid is 0.636 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.637 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.629 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.631 IPB_RECORD: 1582; CONFIDENCE confident structure Scopoletin is an inhibitor of acetylcholinesterase (AChE). Scopoletin is an inhibitor of acetylcholinesterase (AChE).

   

Piperin

InChI=1\C17H19NO3\c19-17(18-10-4-1-5-11-18)7-3-2-6-14-8-9-15-16(12-14)21-13-20-15\h2-3,6-9,12H,1,4-5,10-11,13H2\b6-2+,7-3

C17H19NO3 (285.1365)


C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D004791 - Enzyme Inhibitors > D065607 - Cytochrome P-450 Enzyme Inhibitors Piperine, a natural alkaloid isolated from Piper nigrum L, inhibits P-glycoprotein and CYP3A4 activities with an IC50 value of 61.94±0.054 μg/mL in HeLa cell. Piperine, a natural alkaloid isolated from Piper nigrum L, inhibits P-glycoprotein and CYP3A4 activities with an IC50 value of 61.94±0.054 μg/mL in HeLa cell.

   

Scopoletol

2H-1-Benzopyran-2-one, 7-hydroxy-6-methoxy- (9CI)

C10H8O4 (192.0423)


Scopoletin is an inhibitor of acetylcholinesterase (AChE). Scopoletin is an inhibitor of acetylcholinesterase (AChE).

   

aglafolin

aglafolin

C28H28O8 (492.1784)


A heterotricyclic compound based on a 2,3,3a,8b-tetrahydro-1H-benzo[b]cyclopenta[d]furan framework substituted by hydroxy groups at positions C-1 and C-8b, a methoxycarbonyl group at C-2, a phenyl group at C-3, a 4-methoxyphenyl group at C-3a and methoxy groups at C-6 and C-8. A platelet aggregation inhibitor found in Aglaia elliptifolia and Aglaia odorata.

   

(2s,3r,5s,6r)-6-(2h-1,3-benzodioxol-5-yl)-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-2,3-diol

(2s,3r,5s,6r)-6-(2h-1,3-benzodioxol-5-yl)-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-2,3-diol

C26H24O7 (448.1522)


   

(1r,3as,3bs,4s,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-4,7-diol

(1r,3as,3bs,4s,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-4,7-diol

C29H50O2 (430.3811)


   

(1z,3as,3br,5as,7r,8s,9as,9bs,11as)-1-ethylidene-7,8-dihydroxy-9a,11a-dimethyl-dodecahydro-3h-cyclopenta[a]phenanthren-2-one

(1z,3as,3br,5as,7r,8s,9as,9bs,11as)-1-ethylidene-7,8-dihydroxy-9a,11a-dimethyl-dodecahydro-3h-cyclopenta[a]phenanthren-2-one

C21H32O3 (332.2351)


   

(2e)-n-(4-{[1-hydroxy-2-(4-hydroxyphenyl)ethylidene]amino}butyl)-3-phenylprop-2-enimidic acid

(2e)-n-(4-{[1-hydroxy-2-(4-hydroxyphenyl)ethylidene]amino}butyl)-3-phenylprop-2-enimidic acid

C21H24N2O3 (352.1787)


   

(2s,3r,5s,6r)-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-2,3-diol

(2s,3r,5s,6r)-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-2,3-diol

C26H26O6 (434.1729)


   

(2r,3s,4s)-2-[(1s,3r,6s,8r,11s,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl]-6-methylhept-5-ene-1,3,4-triol

(2r,3s,4s)-2-[(1s,3r,6s,8r,11s,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl]-6-methylhept-5-ene-1,3,4-triol

C30H50O4 (474.3709)


   

(1e,3as,3br,5as,7r,8s,9as,9bs,11as)-1-ethylidene-7,8-dihydroxy-9a,11a-dimethyl-dodecahydro-3h-cyclopenta[a]phenanthren-2-one

(1e,3as,3br,5as,7r,8s,9as,9bs,11as)-1-ethylidene-7,8-dihydroxy-9a,11a-dimethyl-dodecahydro-3h-cyclopenta[a]phenanthren-2-one

C21H32O3 (332.2351)


   

(3r,3as,8as)-3-isopropyl-8a-methyl-8-oxo-1,2,3,3a,6,7-hexahydroazulene-5-carbaldehyde

(3r,3as,8as)-3-isopropyl-8a-methyl-8-oxo-1,2,3,3a,6,7-hexahydroazulene-5-carbaldehyde

C15H22O2 (234.162)


   

(5s,6s)-5-hydroxy-6-[(1s,3r,6s,8r,11s,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl]-2-methylhept-2-en-4-one

(5s,6s)-5-hydroxy-6-[(1s,3r,6s,8r,11s,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl]-2-methylhept-2-en-4-one

C30H48O3 (456.3603)


   

1-(6-methoxy-2,5,5-trimethyloxan-2-yl)-3a,3b,6,6,9a-pentamethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl acetate

1-(6-methoxy-2,5,5-trimethyloxan-2-yl)-3a,3b,6,6,9a-pentamethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl acetate

C33H56O4 (516.4178)


   

n-(4-{[hydroxy(phenyl)methylidene]amino}butyl)-3-phenylprop-2-enimidic acid

n-(4-{[hydroxy(phenyl)methylidene]amino}butyl)-3-phenylprop-2-enimidic acid

C20H22N2O2 (322.1681)


   

(1s,3as,4s,6as)-1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan

(1s,3as,4s,6as)-1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan

C22H26O6 (386.1729)


   

[5-({2-[(1-acetyl-7-isopropyl-4-methyl-octahydroinden-4-yl)oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl}oxy)-3,4-dihydroxyoxolan-3-yl]methyl 4-hydroxy-3,5-dimethoxybenzoate

[5-({2-[(1-acetyl-7-isopropyl-4-methyl-octahydroinden-4-yl)oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl}oxy)-3,4-dihydroxyoxolan-3-yl]methyl 4-hydroxy-3,5-dimethoxybenzoate

C35H52O15 (712.3306)


   

methyl (2s,3r,4r,5s,6r)-6-(2h-1,3-benzodioxol-5-yl)-3-(formyloxy)-2-hydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate

methyl (2s,3r,4r,5s,6r)-6-(2h-1,3-benzodioxol-5-yl)-3-(formyloxy)-2-hydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate

C29H26O10 (534.1526)


   

3-[6,9a,9b-trimethyl-3-(2-methyl-5-oxooxolan-2-yl)-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid

3-[6,9a,9b-trimethyl-3-(2-methyl-5-oxooxolan-2-yl)-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid

C27H42O4 (430.3083)


   

1-(6-methoxy-2,5,5-trimethyloxan-2-yl)-3a,3b,6,6,9a-pentamethyl-dodecahydrocyclopenta[a]phenanthren-7-one

1-(6-methoxy-2,5,5-trimethyloxan-2-yl)-3a,3b,6,6,9a-pentamethyl-dodecahydrocyclopenta[a]phenanthren-7-one

C31H52O3 (472.3916)


   

(2s,3r,5s,6r)-2,10,12-trimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-ol

(2s,3r,5s,6r)-2,10,12-trimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-ol

C27H28O6 (448.1886)


   

n-{4-[(4-hydroxyphenyl)formamido]butyl}-3-phenylprop-2-enimidic acid

n-{4-[(4-hydroxyphenyl)formamido]butyl}-3-phenylprop-2-enimidic acid

C20H22N2O3 (338.163)


   

(2s,3r,4r,5s,6r)-2,3-dihydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboximidic acid

(2s,3r,4r,5s,6r)-2,3-dihydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboximidic acid

C27H27NO7 (477.1787)


   

(1s,3r,6s,7s,8s,11s,12s,15r,16r)-15-[(2r)-1-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,12,16-trimethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

(1s,3r,6s,7s,8s,11s,12s,15r,16r)-15-[(2r)-1-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,12,16-trimethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

C30H50O2 (442.3811)


   

methyl (2s,3r,4r,5s,6r)-6-(2h-1,3-benzodioxol-5-yl)-3-hydroxy-2,10,12-trimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate

methyl (2s,3r,4r,5s,6r)-6-(2h-1,3-benzodioxol-5-yl)-3-hydroxy-2,10,12-trimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate

C29H28O9 (520.1733)


   

(2e)-n-[4-(5-hydroxy-3-methyl-2-oxo-5h-pyrrol-1-yl)butyl]-3-phenylprop-2-enimidic acid

(2e)-n-[4-(5-hydroxy-3-methyl-2-oxo-5h-pyrrol-1-yl)butyl]-3-phenylprop-2-enimidic acid

C18H22N2O3 (314.163)


   

1-(5-ethyl-6-methylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-4,7-diol

1-(5-ethyl-6-methylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-4,7-diol

C29H50O2 (430.3811)


   

(2s,3r,5s,6r)-6-(2h-1,3-benzodioxol-5-yl)-2,10,12-trimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-ol

(2s,3r,5s,6r)-6-(2h-1,3-benzodioxol-5-yl)-2,10,12-trimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-ol

C27H26O7 (462.1678)


   

(4r)-4-[(3s)-3,4-dihydroxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one

(4r)-4-[(3s)-3,4-dihydroxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one

C13H22O3 (226.1569)


   

[(3s,4s,5s)-5-{[(2s,3r,4s,5s,6r)-2-{[(1s,3ar,4r,7s,7as)-1-acetyl-7-isopropyl-4-methyl-octahydroinden-4-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-hydroxy-3,5-dimethoxybenzoate

[(3s,4s,5s)-5-{[(2s,3r,4s,5s,6r)-2-{[(1s,3ar,4r,7s,7as)-1-acetyl-7-isopropyl-4-methyl-octahydroinden-4-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-3,4-dihydroxyoxolan-3-yl]methyl 4-hydroxy-3,5-dimethoxybenzoate

C35H52O15 (712.3306)


   

3-[(3s,3ar,5ar,6s,7s,9ar,9br)-6,9a,9b-trimethyl-3-[(2s)-2-methyl-5-oxooxolan-2-yl]-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid

3-[(3s,3ar,5ar,6s,7s,9ar,9br)-6,9a,9b-trimethyl-3-[(2s)-2-methyl-5-oxooxolan-2-yl]-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid

C27H42O4 (430.3083)


   

(2r,3s,4r)-4-[(1s,3r,6s,8r,11s,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl]-2-(2-methylprop-1-en-1-yl)oxolan-3-ol

(2r,3s,4r)-4-[(1s,3r,6s,8r,11s,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl]-2-(2-methylprop-1-en-1-yl)oxolan-3-ol

C30H48O3 (456.3603)


   

methyl (2s,3r,4r,5s,6r)-3-(formyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate

methyl (2s,3r,4r,5s,6r)-3-(formyloxy)-2-hydroxy-10,12-dimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate

C29H28O9 (520.1733)


   

(1s,3ar,3br,5ar,9ar,9br,11ar)-1-[(2s,6s)-6-methoxy-2,5,5-trimethyloxan-2-yl]-3a,3b,6,6,9a-pentamethyl-dodecahydrocyclopenta[a]phenanthren-7-one

(1s,3ar,3br,5ar,9ar,9br,11ar)-1-[(2s,6s)-6-methoxy-2,5,5-trimethyloxan-2-yl]-3a,3b,6,6,9a-pentamethyl-dodecahydrocyclopenta[a]phenanthren-7-one

C31H52O3 (472.3916)


   

3-{3-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl}propanoic acid

3-{3-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl}propanoic acid

C30H50O4 (474.3709)


   

(1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r)-1-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

(1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r)-1-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

C31H52O2 (456.3967)


   

n-(4-{[1-hydroxy-2-(4-hydroxyphenyl)ethylidene]amino}butyl)-3-phenylprop-2-enimidic acid

n-(4-{[1-hydroxy-2-(4-hydroxyphenyl)ethylidene]amino}butyl)-3-phenylprop-2-enimidic acid

C21H24N2O3 (352.1787)


   

methyl (2s,3r,4r,5s,6r)-3-hydroxy-2,10,12-trimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate

methyl (2s,3r,4r,5s,6r)-3-hydroxy-2,10,12-trimethoxy-6-(4-methoxyphenyl)-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate

C29H30O8 (506.1941)


   

(2e)-n-{4-[(4-hydroxyphenyl)formamido]butyl}-3-phenylprop-2-enimidic acid

(2e)-n-{4-[(4-hydroxyphenyl)formamido]butyl}-3-phenylprop-2-enimidic acid

C20H22N2O3 (338.163)


   

(2e)-n-(4-{[hydroxy(phenyl)methylidene]amino}butyl)-3-phenylprop-2-enimidic acid

(2e)-n-(4-{[hydroxy(phenyl)methylidene]amino}butyl)-3-phenylprop-2-enimidic acid

C20H22N2O2 (322.1681)


   

(1s,3ar,3br,5ar,7r,9ar,9br,11ar)-1-[(2s,6s)-6-methoxy-2,5,5-trimethyloxan-2-yl]-3a,3b,6,6,9a-pentamethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl acetate

(1s,3ar,3br,5ar,7r,9ar,9br,11ar)-1-[(2s,6s)-6-methoxy-2,5,5-trimethyloxan-2-yl]-3a,3b,6,6,9a-pentamethyl-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl acetate

C33H56O4 (516.4178)


   

methyl (2s,3r,4r,5s,6r)-6-(2h-1,3-benzodioxol-5-yl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate

methyl (2s,3r,4r,5s,6r)-6-(2h-1,3-benzodioxol-5-yl)-2,3-dihydroxy-10,12-dimethoxy-5-phenyl-7-oxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-triene-4-carboxylate

C28H26O9 (506.1577)


   

3-hydroxy-5,7-dimethoxy-2-(4-methoxyphenyl)chromen-4-one

3-hydroxy-5,7-dimethoxy-2-(4-methoxyphenyl)chromen-4-one

C18H16O6 (328.0947)


   

1-ethylidene-7,8-dihydroxy-9a,11a-dimethyl-dodecahydro-3h-cyclopenta[a]phenanthren-2-one

1-ethylidene-7,8-dihydroxy-9a,11a-dimethyl-dodecahydro-3h-cyclopenta[a]phenanthren-2-one

C21H32O3 (332.2351)


   

(2e)-n-[4-({[(1s,9s,10s,11r)-1,12-dihydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-11-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-trien-10-yl](hydroxy)methylidene}amino)butyl]-4-hydroxy-2-methylbut-2-enimidic acid

(2e)-n-[4-({[(1s,9s,10s,11r)-1,12-dihydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-11-phenyl-8-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-trien-10-yl](hydroxy)methylidene}amino)butyl]-4-hydroxy-2-methylbut-2-enimidic acid

C36H42N2O9 (646.289)