NCBI Taxonomy: 49078

Leontopodium alpinum (ncbi_taxid: 49078)

found 159 associated metabolites at species taxonomy rank level.

Ancestor: Leontopodium

Child Taxonomies: none taxonomy data.

Chlorogenic acid

Chlorogenic acid (constituent of echinacea angustifolia root, echinacea pallida root, echinacea purpurea root and echinacea purpurea aerial parts)

C16H18O9 (354.0950778)


Chlorogenic acid is a cinnamate ester obtained by formal condensation of the carboxy group of trans-caffeic acid with the 3-hydroxy group of quinic acid. It is an intermediate metabolite in the biosynthesis of lignin. It has a role as a plant metabolite and a food component. It is a cinnamate ester and a tannin. It is functionally related to a (-)-quinic acid and a trans-caffeic acid. It is a conjugate acid of a chlorogenate. Chlorogenic Acid has been used in trials studying the treatment of Advanced Cancer and Impaired Glucose Tolerance. Chlorogenic Acid is a natural product found in Pavetta indica, Fragaria nipponica, and other organisms with data available. Chlorogenic Acid is a polyphenol and the ester of caffeic acid and quinic acid that is found in coffee and black tea, with potential antioxidant and chemopreventive activities. Chlorogenic acid scavenges free radicals, which inhibits DNA damage and may protect against the induction of carcinogenesis. In addition, this agent may upregulate the expression of genes involved in the activation of the immune system and enhances activation and proliferation of cytotoxic T-lymphocytes, macrophages, and natural killer cells. Chlorogenic acid also inhibits the activity of matrix metalloproteinases. A naturally occurring phenolic acid which is a carcinogenic inhibitor. It has also been shown to prevent paraquat-induced oxidative stress in rats. (From J Chromatogr A 1996;741(2):223-31; Biosci Biotechnol Biochem 1996;60(5):765-68). See also: Arctium lappa Root (part of); Cynara scolymus leaf (part of); Lonicera japonica flower (part of) ... View More ... Chlorogenic acid is an ester of caffeic acid and quinic acid. Chlorogenic acid is the major polyphenolic compound in coffee, isolated from the leaves and fruits of dicotyledonous plants. This compound, long known as an antioxidant, also slows the release of glucose into the bloodstream after a meal. Coffee is a complex mixture of chemicals that provides significant amounts of chlorogenic acid. The chlorogenic acid content of a 200 ml (7-oz) cup of coffee has been reported to range from 70-350 mg, which would provide about 35-175 mg of caffeic acid. The results of epidemiological research suggest that coffee consumption may help prevent several chronic diseases, including type 2 diabetes mellitus, Parkinsons disease and liver disease (cirrhosis and hepatocellular carcinoma). Most prospective cohort studies have not found coffee consumption to be associated with significantly increased cardiovascular disease risk. However, coffee consumption is associated with increases in several cardiovascular disease risk factors, including blood pressure and plasma homocysteine. At present, there is little evidence that coffee consumption increases the risk of cancer. (PMID:16507475, 17368041). A cinnamate ester obtained by formal condensation of the carboxy group of trans-caffeic acid with the 3-hydroxy group of quinic acid. It is an intermediate metabolite in the biosynthesis of lignin. [Raw Data] CBA08_Chlorogenic-aci_pos_10eV_1-1_01_209.txt [Raw Data] CBA08_Chlorogenic-aci_neg_30eV_1-1_01_218.txt [Raw Data] CBA08_Chlorogenic-aci_neg_20eV_1-1_01_217.txt [Raw Data] CBA08_Chlorogenic-aci_pos_30eV_1-1_01_211.txt [Raw Data] CBA08_Chlorogenic-aci_neg_40eV_1-1_01_219.txt [Raw Data] CBA08_Chlorogenic-aci_pos_20eV_1-1_01_210.txt [Raw Data] CBA08_Chlorogenic-aci_pos_50eV_1-1_01_213.txt [Raw Data] CBA08_Chlorogenic-aci_neg_50eV_1-1_01_220.txt [Raw Data] CBA08_Chlorogenic-aci_neg_10eV_1-1_01_216.txt [Raw Data] CBA08_Chlorogenic-aci_pos_40eV_1-1_01_212.txt Chlorogenic acid is a major phenolic compound in Lonicera japonica Thunb.. It plays several important and therapeutic roles such as antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension. Chlorogenic acid is a major phenolic compound in Lonicera japonica Thunb. It is an orally active antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension compound[1][2][3]. Chlorogenic acid is a major phenolic compound in Lonicera japonica Thunb.. It plays several important and therapeutic roles such as antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension.

   

beta-Sitosterol

(3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

C29H50O (414.386145)


beta-Sitosterol, a main dietary phytosterol found in plants, may have the potential for prevention and therapy for human cancer. Phytosterols are plant sterols found in foods such as oils, nuts, and vegetables. Phytosterols, in the same way as cholesterol, contain a double bond and are susceptible to oxidation, and are characterized by anti-carcinogenic and anti-atherogenic properties (PMID:13129445, 11432711). beta-Sitosterol is a phytopharmacological extract containing a mixture of phytosterols, with smaller amounts of other sterols, bonded with glucosides. These phytosterols are commonly derived from the South African star grass, Hypoxis rooperi, or from species of Pinus and Picea. The purported active constituent is termed beta-sitosterol. Additionally, the quantity of beta-sitosterol-beta-D-glucoside is often reported. Although the exact mechanism of action of beta-sitosterols is unknown, it may be related to cholesterol metabolism or anti-inflammatory effects (via interference with prostaglandin metabolism). Compared with placebo, beta-sitosterol improved urinary symptom scores and flow measures (PMID:10368239). A plant food-based diet modifies the serum beta-sitosterol concentration in hyperandrogenic postmenopausal women. This finding indicates that beta-sitosterol can be used as a biomarker of exposure in observational studies or as a compliance indicator in dietary intervention studies of cancer prevention (PMID:14652381). beta-Sitosterol induces apoptosis and activates key caspases in MDA-MB-231 human breast cancer cells (PMID:12579296). Sitosterol is a member of the class of phytosterols that is stigmast-5-ene substituted by a beta-hydroxy group at position 3. It has a role as a sterol methyltransferase inhibitor, an anticholesteremic drug, an antioxidant, a plant metabolite and a mouse metabolite. It is a 3beta-sterol, a stigmastane sterol, a 3beta-hydroxy-Delta(5)-steroid, a C29-steroid and a member of phytosterols. It derives from a hydride of a stigmastane. Active fraction of Solanum trilobatum; reduces side-effects of radiation-induced toxicity. Beta-Sitosterol is a natural product found in Elodea canadensis, Ophiopogon intermedius, and other organisms with data available. beta-Sitosterol is one of several phytosterols (plant sterols) with chemical structures similar to that of cholesterol. Sitosterols are white, waxy powders with a characteristic odor. They are hydrophobic and soluble in alcohols. beta-Sitosterol is found in many foods, some of which are ginseng, globe artichoke, sesbania flower, and common oregano. C1907 - Drug, Natural Product > C28178 - Phytosterol > C68437 - Unsaturated Phytosterol D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents D009676 - Noxae > D000963 - Antimetabolites Beta-Sitosterol (purity>98\\%) is a plant sterol. Beta-Sitosterol (purity>98\\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1]. Beta-Sitosterol (purity>98\%) is a plant sterol. Beta-Sitosterol (purity>98\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1].

   

3,4-Di-O-caffeoylquinic acid

(1S,3R,4R,5R)-3,4-bis({[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy})-1,5-dihydroxycyclohexane-1-carboxylic acid

C25H24O12 (516.1267703999999)


Isolated from coffee and maté. 3,4-Dicaffeoylquinic acid is found in many foods, some of which are robusta coffee, arabica coffee, coffee, and coffee and coffee products. 3,4-Di-O-caffeoylquinic acid is found in arabica coffee. 3,4-Di-O-caffeoylquinic acid is isolated from coffe 3,4-Dicaffeoylquinic acid (3,4-Di-O-caffeoylquinic acid), naturally isolated from Laggera alata, has antioxidative, DNA protective, neuroprotective and hepatoprotective properties. 3,4-Dicaffeoylquinic acid exerts apoptosis-mediated cytotoxicity and α-glucosidase inhibitory effects. 3,4-Dicaffeoylquinic acid possesses a unique mechanism of anti-influenza viral activity, that is, enhancing viral clearance by increasing TRAIL[1][2][3]. 3,4-Dicaffeoylquinic acid (3,4-Di-O-caffeoylquinic acid), naturally isolated from Laggera alata, has antioxidative, DNA protective, neuroprotective and hepatoprotective properties. 3,4-Dicaffeoylquinic acid exerts apoptosis-mediated cytotoxicity and α-glucosidase inhibitory effects. 3,4-Dicaffeoylquinic acid possesses a unique mechanism of anti-influenza viral activity, that is, enhancing viral clearance by increasing TRAIL[1][2][3].

   

alpha-Cadinol

(1R,4S,4aR,8aR)-1,6-dimethyl-4-(propan-2-yl)-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-ol

C15H26O (222.1983546)


alpha-Cadinol is found in cloves. alpha-Cadinol is a constituent of Juniperus communis (juniper)

   
   

Cedrelanol

(1S,4S,4aR,8aR)-1,6-dimethyl-4-(propan-2-yl)-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-ol

C15H26O (222.1983546)


A cadinane sesquiterpenoid that is cadin-4-ene carrying a hydroxy substituent at position 10.

   

Cedrelanol

(1S,4S,4aR,8aR)-1,6-dimethyl-4-(propan-2-yl)-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-ol

C15H26O (222.1983546)


Constituent of Juniperus communis (juniper). Cedrelanol is found in many foods, some of which are fruits, sweet basil, lemon balm, and hyssop. Cedrelanol is found in fruits. Cedrelanol is a constituent of Juniperus communis (juniper).

   

Isochlorogenic acid b

3,4-bis({[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy})-1,5-dihydroxycyclohexane-1-carboxylic acid

C25H24O12 (516.1267703999999)


   

delta-Cadinol

(8R)-2,5-dimethyl-8-(propan-2-yl)-1,2,3,4,4a,7,8,8a-octahydronaphthalen-2-ol

C15H26O (222.1983546)


Delta-cadinol, also known as delta-cadinol, is a member of the class of compounds known as sesquiterpenoids. Sesquiterpenoids are terpenes with three consecutive isoprene units. Delta-cadinol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Delta-cadinol is a herbal tasting compound and can be found in a number of food items such as cloves, parsley, lemon balm, and common sage, which makes delta-cadinol a potential biomarker for the consumption of these food products. Delta-cadinol, also known as δ-cadinol, is a member of the class of compounds known as sesquiterpenoids. Sesquiterpenoids are terpenes with three consecutive isoprene units. Delta-cadinol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Delta-cadinol is a herbal tasting compound and can be found in a number of food items such as cloves, parsley, lemon balm, and common sage, which makes delta-cadinol a potential biomarker for the consumption of these food products.

   

4,5-Dicaffeoylquinic acid

(1R,3R,4R,5S)-3,4-bis({[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy})-1,5-dihydroxycyclohexane-1-carboxylic acid

C25H24O12 (516.1267703999999)


   

3,4-Di-O-caffeoylquinic acid

Cyclohexanecarboxylic acid, 3,4-bis(((2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl)oxy)-1,5-dihydroxy-, (1S,3R,4R,5R)-

C25H24O12 (516.1267703999999)


Isochlorogenic acid b is a quinic acid. 3,4-Dicaffeoylquinic acid is a natural product found in Centaurea bracteata, Strychnos axillaris, and other organisms with data available. See also: Lonicera japonica flower (part of); Stevia rebaudiuna Leaf (part of). Isolated from coffee and maté. 3,4-Dicaffeoylquinic acid is found in many foods, some of which are robusta coffee, arabica coffee, coffee, and coffee and coffee products. 3,4-Di-O-caffeoylquinic acid is found in arabica coffee. 3,4-Di-O-caffeoylquinic acid is isolated from coffe 3,4-Dicaffeoylquinic acid (3,4-Di-O-caffeoylquinic acid), naturally isolated from Laggera alata, has antioxidative, DNA protective, neuroprotective and hepatoprotective properties. 3,4-Dicaffeoylquinic acid exerts apoptosis-mediated cytotoxicity and α-glucosidase inhibitory effects. 3,4-Dicaffeoylquinic acid possesses a unique mechanism of anti-influenza viral activity, that is, enhancing viral clearance by increasing TRAIL[1][2][3]. 3,4-Dicaffeoylquinic acid (3,4-Di-O-caffeoylquinic acid), naturally isolated from Laggera alata, has antioxidative, DNA protective, neuroprotective and hepatoprotective properties. 3,4-Dicaffeoylquinic acid exerts apoptosis-mediated cytotoxicity and α-glucosidase inhibitory effects. 3,4-Dicaffeoylquinic acid possesses a unique mechanism of anti-influenza viral activity, that is, enhancing viral clearance by increasing TRAIL[1][2][3].

   

3,4-Di-O-caffeoylquinic acid

Cyclohexanecarboxylic acid, 3,4-bis(((2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl)oxy)-1,5-dihydroxy-, (1S,3R,4R,5R)-

C25H24O12 (516.1267703999999)


Isochlorogenic acid b is a quinic acid. 3,4-Dicaffeoylquinic acid is a natural product found in Centaurea bracteata, Strychnos axillaris, and other organisms with data available. See also: Lonicera japonica flower (part of); Stevia rebaudiuna Leaf (part of). Isolated from coffee and maté. 3,4-Dicaffeoylquinic acid is found in many foods, some of which are robusta coffee, arabica coffee, coffee, and coffee and coffee products. 3,4-Di-O-caffeoylquinic acid is found in arabica coffee. 3,4-Di-O-caffeoylquinic acid is isolated from coffe 3,4-Dicaffeoylquinic acid (3,4-Di-O-caffeoylquinic acid), naturally isolated from Laggera alata, has antioxidative, DNA protective, neuroprotective and hepatoprotective properties. 3,4-Dicaffeoylquinic acid exerts apoptosis-mediated cytotoxicity and α-glucosidase inhibitory effects. 3,4-Dicaffeoylquinic acid possesses a unique mechanism of anti-influenza viral activity, that is, enhancing viral clearance by increasing TRAIL[1][2][3]. 3,4-Dicaffeoylquinic acid (3,4-Di-O-caffeoylquinic acid), naturally isolated from Laggera alata, has antioxidative, DNA protective, neuroprotective and hepatoprotective properties. 3,4-Dicaffeoylquinic acid exerts apoptosis-mediated cytotoxicity and α-glucosidase inhibitory effects. 3,4-Dicaffeoylquinic acid possesses a unique mechanism of anti-influenza viral activity, that is, enhancing viral clearance by increasing TRAIL[1][2][3].

   

Isocomene

Berkheyaradulene

C15H24 (204.18779039999998)


   

sitosterol

17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

C29H50O (414.386145)


A member of the class of phytosterols that is stigmast-5-ene substituted by a beta-hydroxy group at position 3. C1907 - Drug, Natural Product > C28178 - Phytosterol > C68437 - Unsaturated Phytosterol D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents D009676 - Noxae > D000963 - Antimetabolites Beta-Sitosterol (purity>98\\%) is a plant sterol. Beta-Sitosterol (purity>98\\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1]. Beta-Sitosterol (purity>98\%) is a plant sterol. Beta-Sitosterol (purity>98\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1].

   

Chlorogenic Acid

Malonyl-caffeoylquinic acid

C16H18O9 (354.0950778)


IPB_RECORD: 1901; CONFIDENCE confident structure Chlorogenic acid is a major phenolic compound in Lonicera japonica Thunb.. It plays several important and therapeutic roles such as antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension. Chlorogenic acid is a major phenolic compound in Lonicera japonica Thunb. It is an orally active antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension compound[1][2][3]. Chlorogenic acid is a major phenolic compound in Lonicera japonica Thunb.. It plays several important and therapeutic roles such as antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension.

   

ent-Kaur-16-en-19-oic acid

ent-Kaur-16-en-19-oic acid

C20H30O2 (302.224568)


   
   

4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenol

4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenol

C15H26O (222.1983546)


   

Harzol

(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methyl-heptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

C29H50O (414.386145)


C1907 - Drug, Natural Product > C28178 - Phytosterol > C68437 - Unsaturated Phytosterol D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents D009676 - Noxae > D000963 - Antimetabolites Beta-Sitosterol (purity>98\\%) is a plant sterol. Beta-Sitosterol (purity>98\\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1]. Beta-Sitosterol (purity>98\%) is a plant sterol. Beta-Sitosterol (purity>98\%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation[1].

   

Heriguard

Cyclohexanecarboxylic acid, 3-[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-1,4,5-trihydroxy-, [1S-(1.alpha.,3.beta.,4.alpha.,5.alpha.)]-

C16H18O9 (354.0950778)


Chlorogenic acid is a major phenolic compound in Lonicera japonica Thunb.. It plays several important and therapeutic roles such as antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension. Chlorogenic acid is a major phenolic compound in Lonicera japonica Thunb. It is an orally active antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension compound[1][2][3]. Chlorogenic acid is a major phenolic compound in Lonicera japonica Thunb.. It plays several important and therapeutic roles such as antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension.

   

(-)-alpha-Isocomene

(-)-alpha-Isocomene

C15H24 (204.18779039999998)


A tricyclic sesquiterpene that is 1,2,3,3a,5a,6,7,8-octahydrocyclopenta[c]pentalene bearing four methyl substituents at positions 1, 3a, 4 and 5a.

   
   

Tauro-omega-muricholic acid

Tauro-omega-muricholic acid

C26H45NO7S (515.291658)


   

(1s,5r,8r,11s)-5,7,7,11-tetramethyltricyclo[6.3.0.0¹,⁵]undec-2-ene

(1s,5r,8r,11s)-5,7,7,11-tetramethyltricyclo[6.3.0.0¹,⁵]undec-2-ene

C15H24 (204.18779039999998)


   

(1r,2s,4r,5s)-4-(acetyloxy)-2-[(2r,4r)-4-(acetyloxy)-6-methylhept-5-en-2-yl]-5-methylcyclohexyl (2z)-2-methylbut-2-enoate

(1r,2s,4r,5s)-4-(acetyloxy)-2-[(2r,4r)-4-(acetyloxy)-6-methylhept-5-en-2-yl]-5-methylcyclohexyl (2z)-2-methylbut-2-enoate

C24H38O6 (422.2668248)


   

(4s,6s)-2-methyl-6-[(1r,2s,5r,6s)-2,5,6-tris(acetyloxy)-4-methylcyclohex-3-en-1-yl]hept-2-en-4-yl (2z)-2-methylbut-2-enoate

(4s,6s)-2-methyl-6-[(1r,2s,5r,6s)-2,5,6-tris(acetyloxy)-4-methylcyclohex-3-en-1-yl]hept-2-en-4-yl (2z)-2-methylbut-2-enoate

C26H38O8 (478.2566548)


   

(1r,2r,5s,8s)-2,5,8-trimethyl-6-methylidenetricyclo[6.3.0.0¹,⁵]undecane

(1r,2r,5s,8s)-2,5,8-trimethyl-6-methylidenetricyclo[6.3.0.0¹,⁵]undecane

C15H24 (204.18779039999998)


   

(2s)-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

(2s)-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C14H12O4 (244.0735552)


   

4-(acetyloxy)-6-[4-(acetyloxy)-6-methylhept-5-en-2-yl]-3-methylcyclohex-2-en-1-yl 2-methylbut-2-enoate

4-(acetyloxy)-6-[4-(acetyloxy)-6-methylhept-5-en-2-yl]-3-methylcyclohex-2-en-1-yl 2-methylbut-2-enoate

C24H36O6 (420.2511756)


   

4-(acetyloxy)-2-[4-(acetyloxy)-6-methylhept-5-en-2-yl]-5-methylcyclohexyl 2-methylbut-2-enoate

4-(acetyloxy)-2-[4-(acetyloxy)-6-methylhept-5-en-2-yl]-5-methylcyclohexyl 2-methylbut-2-enoate

C24H38O6 (422.2668248)


   

2,6-dimethyl-2,3-dihydro-1-benzopyran-4-one

2,6-dimethyl-2,3-dihydro-1-benzopyran-4-one

C11H12O2 (176.0837252)


   

{2,5,9-trimethyltricyclo[6.3.0.0¹,⁵]undec-3-en-3-yl}methyl acetate

{2,5,9-trimethyltricyclo[6.3.0.0¹,⁵]undec-3-en-3-yl}methyl acetate

C17H26O2 (262.1932696)


   

[(1s,2r,5s,8s,9r)-2,5,9-trimethyltricyclo[6.3.0.0¹,⁵]undec-3-en-3-yl]methyl acetate

[(1s,2r,5s,8s,9r)-2,5,9-trimethyltricyclo[6.3.0.0¹,⁵]undec-3-en-3-yl]methyl acetate

C17H26O2 (262.1932696)


   

2,5,8-trimethyl-6-methylidenetricyclo[6.3.0.0¹,⁵]undecane

2,5,8-trimethyl-6-methylidenetricyclo[6.3.0.0¹,⁵]undecane

C15H24 (204.18779039999998)


   

[(1r,2r,5s,8s)-2,6,8-trimethyltricyclo[6.3.0.0¹,⁵]undec-6-en-5-yl]methyl acetate

[(1r,2r,5s,8s)-2,6,8-trimethyltricyclo[6.3.0.0¹,⁵]undec-6-en-5-yl]methyl acetate

C17H26O2 (262.1932696)


   

[(1r,2s,5s,8r)-2,6,8-trimethyltricyclo[6.3.0.0¹,⁵]undec-6-en-5-yl]methyl acetate

[(1r,2s,5s,8r)-2,6,8-trimethyltricyclo[6.3.0.0¹,⁵]undec-6-en-5-yl]methyl acetate

C17H26O2 (262.1932696)


   

{4-[(3,4-dimethoxyphenyl)methyl]-2-(3,4,5-trimethoxyphenyl)oxolan-3-yl}methyl 2-methylbut-2-enoate

{4-[(3,4-dimethoxyphenyl)methyl]-2-(3,4,5-trimethoxyphenyl)oxolan-3-yl}methyl 2-methylbut-2-enoate

C28H36O8 (500.2410056)


   

methyl 2,10-dihydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate

methyl 2,10-dihydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate

C26H38O6 (446.2668248)


   

(1s,4r,6s)-4-(acetyloxy)-6-[(2r,4r)-4-(acetyloxy)-6-methylhept-5-en-2-yl]-3-methylcyclohex-2-en-1-yl (2z)-2-methylbut-2-enoate

(1s,4r,6s)-4-(acetyloxy)-6-[(2r,4r)-4-(acetyloxy)-6-methylhept-5-en-2-yl]-3-methylcyclohex-2-en-1-yl (2z)-2-methylbut-2-enoate

C24H36O6 (420.2511756)


   

1-[2-(3-hydroxyprop-1-en-2-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3-dihydro-1-benzofuran-5-yl]ethanone

1-[2-(3-hydroxyprop-1-en-2-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3-dihydro-1-benzofuran-5-yl]ethanone

C19H24O9 (396.14202539999997)


   

2-[4-(acetyloxy)-6-methylhept-5-en-2-yl]-4-hydroxy-5-methylcyclohexyl 2-methylbut-2-enoate

2-[4-(acetyloxy)-6-methylhept-5-en-2-yl]-4-hydroxy-5-methylcyclohexyl 2-methylbut-2-enoate

C22H36O5 (380.2562606)


   

2,4,4,8-tetramethyltricyclo[3.3.3.0¹,⁵]undec-2-ene

2,4,4,8-tetramethyltricyclo[3.3.3.0¹,⁵]undec-2-ene

C15H24 (204.18779039999998)


   

10,10-dimethyl-2,6-dimethylidenebicyclo[7.2.0]undecan-5-yl acetate

10,10-dimethyl-2,6-dimethylidenebicyclo[7.2.0]undecan-5-yl acetate

C17H26O2 (262.1932696)


   

[(1r,2r,5r,8s)-2,6,8-trimethyltricyclo[6.3.0.0¹,⁵]undec-6-en-5-yl]methyl acetate

[(1r,2r,5r,8s)-2,6,8-trimethyltricyclo[6.3.0.0¹,⁵]undec-6-en-5-yl]methyl acetate

C17H26O2 (262.1932696)


   

(1r,5s,9s)-10,10-dimethyl-2,6-dimethylidenebicyclo[7.2.0]undecan-5-yl acetate

(1r,5s,9s)-10,10-dimethyl-2,6-dimethylidenebicyclo[7.2.0]undecan-5-yl acetate

C17H26O2 (262.1932696)


   

methyl (1r,2s,5s,8r)-2,6,8-trimethyltricyclo[6.3.0.0¹,⁵]undec-6-ene-5-carboxylate

methyl (1r,2s,5s,8r)-2,6,8-trimethyltricyclo[6.3.0.0¹,⁵]undec-6-ene-5-carboxylate

C16H24O2 (248.1776204)


   

[(1r,2r,5s)-6,6,8-trimethyltricyclo[3.3.3.0¹,⁵]undec-7-en-2-yl]methyl acetate

[(1r,2r,5s)-6,6,8-trimethyltricyclo[3.3.3.0¹,⁵]undec-7-en-2-yl]methyl acetate

C17H26O2 (262.1932696)


   

{6,6,8-trimethyltricyclo[3.3.3.0¹,⁵]undec-7-en-2-yl}methyl acetate

{6,6,8-trimethyltricyclo[3.3.3.0¹,⁵]undec-7-en-2-yl}methyl acetate

C17H26O2 (262.1932696)


   

[(2s,3r,4r)-2-(3,4-dimethoxyphenyl)-4-[(3,4-dimethoxyphenyl)methyl]oxolan-3-yl]methyl (2e)-2-methylbut-2-enoate

[(2s,3r,4r)-2-(3,4-dimethoxyphenyl)-4-[(3,4-dimethoxyphenyl)methyl]oxolan-3-yl]methyl (2e)-2-methylbut-2-enoate

C27H34O7 (470.2304414)


   

[(1r,2s,5s,8s,9r)-2,5,9-trimethyltricyclo[6.3.0.0¹,⁵]undec-3-en-3-yl]methyl acetate

[(1r,2s,5s,8s,9r)-2,5,9-trimethyltricyclo[6.3.0.0¹,⁵]undec-3-en-3-yl]methyl acetate

C17H26O2 (262.1932696)


   

(1r,2s,4r,5s)-2-[(2r,4r)-4-(acetyloxy)-6-methylhept-5-en-2-yl]-4-hydroxy-5-methylcyclohexyl (2z)-2-methylbut-2-enoate

(1r,2s,4r,5s)-2-[(2r,4r)-4-(acetyloxy)-6-methylhept-5-en-2-yl]-4-hydroxy-5-methylcyclohexyl (2z)-2-methylbut-2-enoate

C22H36O5 (380.2562606)


   

methyl 2,6,8-trimethyltricyclo[6.3.0.0¹,⁵]undec-6-ene-5-carboxylate

methyl 2,6,8-trimethyltricyclo[6.3.0.0¹,⁵]undec-6-ene-5-carboxylate

C16H24O2 (248.1776204)


   

5,7,7,11-tetramethyltricyclo[6.3.0.0¹,⁵]undec-2-ene

5,7,7,11-tetramethyltricyclo[6.3.0.0¹,⁵]undec-2-ene

C15H24 (204.18779039999998)


   

(1r,2s,5r,8r)-2,5,6,8-tetramethyltricyclo[6.3.0.0¹,⁵]undec-6-ene

(1r,2s,5r,8r)-2,5,6,8-tetramethyltricyclo[6.3.0.0¹,⁵]undec-6-ene

C15H24 (204.18779039999998)


   

{2,6,8-trimethyltricyclo[6.3.0.0¹,⁵]undec-6-en-5-yl}methyl acetate

{2,6,8-trimethyltricyclo[6.3.0.0¹,⁵]undec-6-en-5-yl}methyl acetate

C17H26O2 (262.1932696)


   

stigmast-5-en-3-ol, (3β)-

stigmast-5-en-3-ol, (3β)-

C29H50O (414.386145)


   

2,5,6,8-tetramethyltricyclo[6.3.0.0¹,⁵]undec-6-ene

2,5,6,8-tetramethyltricyclo[6.3.0.0¹,⁵]undec-6-ene

C15H24 (204.18779039999998)


   

methyl (1r,2s,4s,5r,9r,10r,13r,15s)-2,10-dihydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate

methyl (1r,2s,4s,5r,9r,10r,13r,15s)-2,10-dihydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate

C26H38O6 (446.2668248)


   

(2s)-2,6-dimethyl-2,3-dihydro-1-benzopyran-4-one

(2s)-2,6-dimethyl-2,3-dihydro-1-benzopyran-4-one

C11H12O2 (176.0837252)


   

2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C14H12O4 (244.0735552)


   

1-[(2r,3s)-2-(3-hydroxyprop-1-en-2-yl)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3-dihydro-1-benzofuran-5-yl]ethanone

1-[(2r,3s)-2-(3-hydroxyprop-1-en-2-yl)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3-dihydro-1-benzofuran-5-yl]ethanone

C19H24O9 (396.14202539999997)


   

(1r,5s,8r)-2,4,4,8-tetramethyltricyclo[3.3.3.0¹,⁵]undec-2-ene

(1r,5s,8r)-2,4,4,8-tetramethyltricyclo[3.3.3.0¹,⁵]undec-2-ene

C15H24 (204.18779039999998)


   

2,3,4-tris({[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy})-5-[(3-hydroxybutanoyl)oxy]hexanedioic acid

2,3,4-tris({[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy})-5-[(3-hydroxybutanoyl)oxy]hexanedioic acid

C37H34O19 (782.1694214)


   

[(2s,3r,4r)-2-(3,4,5-trimethoxyphenyl)-4-[(3,4,5-trimethoxyphenyl)methyl]oxolan-3-yl]methyl (2z)-2-methylbut-2-enoate

[(2s,3r,4r)-2-(3,4,5-trimethoxyphenyl)-4-[(3,4,5-trimethoxyphenyl)methyl]oxolan-3-yl]methyl (2z)-2-methylbut-2-enoate

C29H38O9 (530.2515698)


   

[(2s,3r,4r)-4-[(3,4-dimethoxyphenyl)methyl]-2-(3,4,5-trimethoxyphenyl)oxolan-3-yl]methyl (2z)-2-methylbut-2-enoate

[(2s,3r,4r)-4-[(3,4-dimethoxyphenyl)methyl]-2-(3,4,5-trimethoxyphenyl)oxolan-3-yl]methyl (2z)-2-methylbut-2-enoate

C28H36O8 (500.2410056)


   

(2s)-10-methoxy-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

(2s)-10-methoxy-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C15H14O5 (274.0841194)


   

[2-(3,4,5-trimethoxyphenyl)-4-[(3,4,5-trimethoxyphenyl)methyl]oxolan-3-yl]methyl 2-methylbut-2-enoate

[2-(3,4,5-trimethoxyphenyl)-4-[(3,4,5-trimethoxyphenyl)methyl]oxolan-3-yl]methyl 2-methylbut-2-enoate

C29H38O9 (530.2515698)


   

(3s,4e,6e)-1-(acetyloxy)tetradeca-4,6-dien-8,10,12-triyn-3-yl (2z)-2-methylbut-2-enoate

(3s,4e,6e)-1-(acetyloxy)tetradeca-4,6-dien-8,10,12-triyn-3-yl (2z)-2-methylbut-2-enoate

C21H22O4 (338.1518012)


   

2-methyl-6-[2,5,6-tris(acetyloxy)-4-methylcyclohex-3-en-1-yl]hept-2-en-4-yl 2-methylbut-2-enoate

2-methyl-6-[2,5,6-tris(acetyloxy)-4-methylcyclohex-3-en-1-yl]hept-2-en-4-yl 2-methylbut-2-enoate

C26H38O8 (478.2566548)


   

[(2r)-6,6,8-trimethyltricyclo[3.3.3.0¹,⁵]undec-7-en-2-yl]methyl acetate

[(2r)-6,6,8-trimethyltricyclo[3.3.3.0¹,⁵]undec-7-en-2-yl]methyl acetate

C17H26O2 (262.1932696)


   

10-methoxy-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

10-methoxy-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C15H14O5 (274.0841194)


   

(2s,3s,4s,5r)-2,3,4-tris({[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy})-5-{[(3s)-3-hydroxybutanoyl]oxy}hexanedioic acid

(2s,3s,4s,5r)-2,3,4-tris({[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy})-5-{[(3s)-3-hydroxybutanoyl]oxy}hexanedioic acid

C37H34O19 (782.1694214)


   

(3s)-1-(acetyloxy)tetradeca-4,6-dien-8,10,12-triyn-3-yl 2-methylbut-2-enoate

(3s)-1-(acetyloxy)tetradeca-4,6-dien-8,10,12-triyn-3-yl 2-methylbut-2-enoate

C21H22O4 (338.1518012)