NCBI Taxonomy: 307241

Mansonia (ncbi_taxid: 307241)

found 62 associated metabolites at genus taxonomy rank level.

Ancestor: Helicteroideae

Child Taxonomies: Mansonia gagei, Mansonia altissima

Acetovanillone

1-(4-hydroxy-3-methoxyphenyl)ethan-1-one

C9H10O3 (166.062991)


Acetovanillone, also known as 4-hydroxy-3-methoxyacetophenone or acetoguaiacon, is a member of the class of compounds known as alkyl-phenylketones. Alkyl-phenylketones are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. Acetovanillone is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Acetovanillone is a faint, sweet, and vanillin tasting compound found in corn and garden onion, which makes acetovanillone a potential biomarker for the consumption of these food products. Acetovanillone may be a unique S.cerevisiae (yeast) metabolite. D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D020011 - Protective Agents > D000975 - Antioxidants D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents D004791 - Enzyme Inhibitors Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5]. Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5]. Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5].

   

Mansonone C

3,8-Dimethyl-5-isopropyl-1,2-naphthalenedione

C15H16O2 (228.1150236)


   

Apocynin

InChI=1/C9H10O3/c1-6(10)7-3-4-8(11)9(5-7)12-2/h3-5,11H,1-2H

C9H10O3 (166.062991)


Apocynin is an aromatic ketone that is 1-phenylethanone substituted by a hydroxy group at position 4 and a methoxy group at position 3. It has a role as a non-narcotic analgesic, a non-steroidal anti-inflammatory drug, an antirheumatic drug, a peripheral nervous system drug, an EC 1.6.3.1. [NAD(P)H oxidase (H2O2-forming)] inhibitor and a plant metabolite. It is a member of acetophenones, a methyl ketone and an aromatic ketone. Acetovanillone has been used in trials studying the treatment of Bronchial Asthma and Chronic Obstructive Pulmonary Disease. Acetovanillone is a natural product found in Iris tectorum, Apocynum cannabinum, and other organisms with data available. Acetovanillone is a metabolite found in or produced by Saccharomyces cerevisiae. An aromatic ketone that is 1-phenylethanone substituted by a hydroxy group at position 4 and a methoxy group at position 3. D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D020011 - Protective Agents > D000975 - Antioxidants D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents D004791 - Enzyme Inhibitors Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5]. Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5]. Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5].

   

5-hydroxy-5-isopropyl-3,8-dimethyl-7,8-dihydronaphthalene-1,2,6-trione

5-hydroxy-5-isopropyl-3,8-dimethyl-7,8-dihydronaphthalene-1,2,6-trione

C15H18O4 (262.1205028)


   

apocynin

InChI=1\C9H10O3\c1-6(10)7-3-4-8(11)9(5-7)12-2\h3-5,11H,1-2H

C9H10O3 (166.062991)


D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D020011 - Protective Agents > D000975 - Antioxidants D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents D004791 - Enzyme Inhibitors Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5]. Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5]. Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5].

   

(1r,4r)-1,5-dihydroxy-1-isopropyl-6-methoxy-4,7-dimethyl-3,4-dihydronaphthalen-2-one

(1r,4r)-1,5-dihydroxy-1-isopropyl-6-methoxy-4,7-dimethyl-3,4-dihydronaphthalen-2-one

C16H22O4 (278.1518012)


   

5-isopropyl-3,8-dimethyl-5,6,7,8-tetrahydronaphthalene-1,2-dione

5-isopropyl-3,8-dimethyl-5,6,7,8-tetrahydronaphthalene-1,2-dione

C15H20O2 (232.14632200000003)


   

6-hydroxy-5-isopropyl-3,8-dimethylchromen-2-one

6-hydroxy-5-isopropyl-3,8-dimethylchromen-2-one

C14H16O3 (232.1099386)


   

(8r)-4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

(8r)-4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

C14H14O3 (230.0942894)


   

4,8,12-trimethyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),3,5(13),6,8-pentaene-10,11-dione

4,8,12-trimethyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),3,5(13),6,8-pentaene-10,11-dione

C15H12O3 (240.0786402)


   

4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

C14H14O3 (230.0942894)


   

(4r)-6-hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),5,7,9(13)-tetraene-10,11-dione

(4r)-6-hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),5,7,9(13)-tetraene-10,11-dione

C15H14O4 (258.0892044)


   

6-hydroxy-5-isopropyl-3,8-dimethylnaphthalene-1,2-dione

6-hydroxy-5-isopropyl-3,8-dimethylnaphthalene-1,2-dione

C15H16O3 (244.1099386)


   

(2r,3s)-2,6-dihydroxy-5-isopropyl-3,8-dimethyl-3,4-dihydro-2h-naphthalen-1-one

(2r,3s)-2,6-dihydroxy-5-isopropyl-3,8-dimethyl-3,4-dihydro-2h-naphthalen-1-one

C15H20O3 (248.14123700000002)


   

(8r)-10-hydroxy-4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

(8r)-10-hydroxy-4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

C14H14O4 (246.0892044)


   

(8r)-8-hydroxy-4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

(8r)-8-hydroxy-4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

C14H14O4 (246.0892044)


   

6-hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),5,7,9(13)-tetraene-10,11-dione

6-hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),5,7,9(13)-tetraene-10,11-dione

C15H14O4 (258.0892044)


   

5-isopropyl-6-methoxy-3,8-dimethylchromen-2-one

5-isopropyl-6-methoxy-3,8-dimethylchromen-2-one

C15H18O3 (246.1255878)


   

(1r,4s)-1,5,6-trihydroxy-1-isopropyl-4,7-dimethyl-3,4-dihydronaphthalen-2-one

(1r,4s)-1,5,6-trihydroxy-1-isopropyl-4,7-dimethyl-3,4-dihydronaphthalen-2-one

C15H20O4 (264.13615200000004)


   

(8s)-1-hydroxy-5-isopropyl-3,8-dimethyl-7,8-dihydronaphthalene-2,6-dione

(8s)-1-hydroxy-5-isopropyl-3,8-dimethyl-7,8-dihydronaphthalene-2,6-dione

C15H18O3 (246.1255878)


   

(8r)-10-methoxy-4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

(8r)-10-methoxy-4,8,12-trimethyl-2,6-dioxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),4,9(13),10-tetraen-3-one

C15H16O4 (260.1048536)


   

(4r)-4-hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),5,7,9(13)-tetraene-10,11-dione

(4r)-4-hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(12),5,7,9(13)-tetraene-10,11-dione

C15H14O4 (258.0892044)


   

(5r,8r)-5-hydroxy-5-isopropyl-3,8-dimethyl-7,8-dihydronaphthalene-1,2,6-trione

(5r,8r)-5-hydroxy-5-isopropyl-3,8-dimethyl-7,8-dihydronaphthalene-1,2,6-trione

C15H18O4 (262.1205028)