NCBI Taxonomy: 132451

Millettia pulchra (ncbi_taxid: 132451)

found 40 associated metabolites at species taxonomy rank level.

Ancestor: Millettia

Child Taxonomies: none taxonomy data.

(-)-Maackiain

(1R,12R)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-ol

C16H12O5 (284.0685)


(-)-maackiain is the (-)-enantiomer of maackiain. It is an enantiomer of a (+)-maackiain. Maackiain is a natural product found in Tephrosia virginiana, Leptolobium bijugum, and other organisms with data available. (-)-Maackiain. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=2035-15-6 (retrieved 2024-07-09) (CAS RN: 2035-15-6). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). (-)-Maackiain is a pterocarpan phytoalexin produced from Sophora flavescens. (-)-Maackiain is toxic to several genera of fungal pathogens of legume and non legume hosts[1]. (-)-Maackiain is a pterocarpan phytoalexin produced from Sophora flavescens. (-)-Maackiain is toxic to several genera of fungal pathogens of legume and non legume hosts[1]. (-)-Maackiain is a pterocarpan phytoalexin produced from Sophora flavescens. (-)-Maackiain is toxic to several genera of fungal pathogens of legume and non legume hosts[1]. (-)-Maackiain is a pterocarpan phytoalexin produced from Sophora flavescens. (-)-Maackiain is toxic to several genera of fungal pathogens of legume and non legume hosts[1].

   

Sophoranone

(2S)-7-hydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-4-chromanone

C30H36O4 (460.2613)


A dihydroxyflavanone that is (2S)-flavanone substituted by hydroxy groups at positions 7 and 4 and prenyl groups at positions 3 and 5 respectively.

   

Karanjin

4H-Furo[2,3-h]-1-benzopyran-4-one, 3-methoxy-2-phenyl-

C18H12O4 (292.0736)


Karanjin is an extended flavonoid. Karanjin is a natural product found in Fordia cauliflora, Millettia pulchra, and other organisms with data available. Karanjin is an orally active furanoflavonoid which can be isolated from several Leguminosae. Karanjin exhibits evident anti-diabetic, anti-cancer, anti-inflammatory, antioxidant, anticolitis, anti-ulcer, anti-Alzheimer properties and multiple insect repellent/insecticidal, acaricide properties, suggesting the potential of Karanjin to be applied to relevant research[1]. Karanjin is a major active furanoflavonol constituent of Fordia cauliflora. Karanjin induces GLUT4 translocation in skeletal muscle cells by increasing AMPK activity. Karanjin can induce cancer cell death through cell cycle arrest and enhance apoptosis[1][2]. Karanjin is a major active furanoflavonol constituent of Fordia cauliflora. Karanjin induces GLUT4 translocation in skeletal muscle cells by increasing AMPK activity. Karanjin can induce cancer cell death through cell cycle arrest and enhance apoptosis[1][2].

   

(-)-Maackiain

5,7,11,19-tetraoxapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13(18),14,16-hexaen-16-ol

C16H12O5 (284.0685)


(-)-Maackiain is found in chickpea. (-)-Maackiain is widespread in the Leguminosae subfamily. (-)-Maackiain is a constituent of Trifolium pratense (red clover). (-)-Maackiain is a pterocarpan phytoalexin produced from Sophora flavescens. (-)-Maackiain is toxic to several genera of fungal pathogens of legume and non legume hosts[1]. (-)-Maackiain is a pterocarpan phytoalexin produced from Sophora flavescens. (-)-Maackiain is toxic to several genera of fungal pathogens of legume and non legume hosts[1]. (-)-Maackiain is a pterocarpan phytoalexin produced from Sophora flavescens. (-)-Maackiain is toxic to several genera of fungal pathogens of legume and non legume hosts[1]. (-)-Maackiain is a pterocarpan phytoalexin produced from Sophora flavescens. (-)-Maackiain is toxic to several genera of fungal pathogens of legume and non legume hosts[1].

   

Karanjin

3-methoxy-2-phenyl-4H-furo(2,3-h)-1-benzopyran-4-one

C18H12O4 (292.0736)


Karanjin is an orally active furanoflavonoid which can be isolated from several Leguminosae. Karanjin exhibits evident anti-diabetic, anti-cancer, anti-inflammatory, antioxidant, anticolitis, anti-ulcer, anti-Alzheimer properties and multiple insect repellent/insecticidal, acaricide properties, suggesting the potential of Karanjin to be applied to relevant research[1]. Karanjin is a major active furanoflavonol constituent of Fordia cauliflora. Karanjin induces GLUT4 translocation in skeletal muscle cells by increasing AMPK activity. Karanjin can induce cancer cell death through cell cycle arrest and enhance apoptosis[1][2]. Karanjin is a major active furanoflavonol constituent of Fordia cauliflora. Karanjin induces GLUT4 translocation in skeletal muscle cells by increasing AMPK activity. Karanjin can induce cancer cell death through cell cycle arrest and enhance apoptosis[1][2].

   

(-)-Isolonchocarpin

(-)-Isolonchocarpin

C20H18O3 (306.1256)


   

Pterocarpin

3-Methoxy-8,9-methylenedioxypterocarpan

C17H14O5 (298.0841)


   

6-Methoxypterocarpin

(6S,6aS,11aR)-3,6-Dimethoxy-8,9-methylenedioxypterocarpan

C18H16O6 (328.0947)


   

6-Methoxyhomopterocarpin

(6S,6aS,11aR) -3,6,9-Trimethoxypterocarpan

C18H18O5 (314.1154)


   

Hydroxysophoranone

5,7,4-Trihydroxy-8,3,5-tri-C-prenylflavanone

C30H36O5 (476.2563)


   

Isopongaflavone

5-Methoxy-8,8-dimethyl-2-phenyl-4H,8H-benzo [ 1,2-b:3,4-b ] dipyran-4-one

C21H18O4 (334.1205)


   

Karanjin

4H-Furo(2,3-h)-1-benzopyran-4-one, 3-methoxy-2-phenyl- (8CI)(9CI)

C18H12O4 (292.0736)


relative retention time with respect to 9-anthracene Carboxylic Acid is 1.329 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.324 Karanjin is an orally active furanoflavonoid which can be isolated from several Leguminosae. Karanjin exhibits evident anti-diabetic, anti-cancer, anti-inflammatory, antioxidant, anticolitis, anti-ulcer, anti-Alzheimer properties and multiple insect repellent/insecticidal, acaricide properties, suggesting the potential of Karanjin to be applied to relevant research[1]. Karanjin is a major active furanoflavonol constituent of Fordia cauliflora. Karanjin induces GLUT4 translocation in skeletal muscle cells by increasing AMPK activity. Karanjin can induce cancer cell death through cell cycle arrest and enhance apoptosis[1][2]. Karanjin is a major active furanoflavonol constituent of Fordia cauliflora. Karanjin induces GLUT4 translocation in skeletal muscle cells by increasing AMPK activity. Karanjin can induce cancer cell death through cell cycle arrest and enhance apoptosis[1][2].

   

8,8-Dimethyl-2-phenyl-4H,8H-benzo[1,2-b:3,4-b]dipyran-4-one

8,8-Dimethyl-2-phenyl-4H,8H-benzo [ 1,2-b:3,4-b ] dipyran-4-one

C20H16O3 (304.1099)


   

Pongachalcone I

Pongachalcone I

C21H20O4 (336.1362)


   

Angustone A

5,7,2,4-Tetrahydroxy-6,3-diprenylisoflavone

C25H26O6 (422.1729)


   

Lonchocarpin

(2E) -1- (5-Hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl) -3-phenyl-2-propen-1-one

C20H18O3 (306.1256)


   

Ovalitenin A

1- (4-Methoxybenzofuran-5-yl) -3-phenyl-2-propen-1-one

C18H14O3 (278.0943)


   

pongamol

(2Z)-3-hydroxy-1-(4-methoxy-1-benzofuran-5-yl)-3-phenylprop-2-en-1-one

C18H14O4 (294.0892)


Pongamol (Lanceolatin C) is potent α-glucosidase inhibitor (IC50=103.5 μM) and has free-radical (DPPH) scavenging,antihyperglycemic, and antihyperglycemic activities[1].

   

8,8-dimethyl-2-phenylpyrano[2,3-f]chromen-4-one

NCGC00385787-01!8,8-dimethyl-2-phenylpyrano[2,3-f]chromen-4-one

C20H16O3 (304.1099)


   

2-phenylfuro[2,3-h]chromen-4-one

NCGC00384489-01!2-phenylfuro[2,3-h]chromen-4-one

C17H10O3 (262.063)


   

8,8-dimethyl-2-phenylpyrano[2,3-f]chromen-4-one

8,8-dimethyl-2-phenylpyrano[2,3-f]chromen-4-one

C20H16O3 (304.1099)


   

Maackiain

(-)-Maackiain

C16H12O5 (284.0685)


Widespread in the Leguminosae subfamily. Constituent of Trifolium pratense (red clover). (-)-Maackiain is found in many foods, some of which are nectarine, chickpea, alaska blueberry, and adzuki bean. (-)-Maackiain is a pterocarpan phytoalexin produced from Sophora flavescens. (-)-Maackiain is toxic to several genera of fungal pathogens of legume and non legume hosts[1]. (-)-Maackiain is a pterocarpan phytoalexin produced from Sophora flavescens. (-)-Maackiain is toxic to several genera of fungal pathogens of legume and non legume hosts[1]. (-)-Maackiain is a pterocarpan phytoalexin produced from Sophora flavescens. (-)-Maackiain is toxic to several genera of fungal pathogens of legume and non legume hosts[1]. (-)-Maackiain is a pterocarpan phytoalexin produced from Sophora flavescens. (-)-Maackiain is toxic to several genera of fungal pathogens of legume and non legume hosts[1].

   

6,6-Dimethylpyrano[2,3:7,8]flavone

8,8-Dimethyl-2-phenyl-4H,8H-pyrano[2,3-f]chromen-4-one

C20H16O3 (304.1099)


   

2-Phenylfuro[2,3-h]chromen-4-one

2-phenylfuro[2,3-h]chromen-4-one

C17H10O3 (262.063)


   

Maackiain

Maackiain

C16H12O5 (284.0685)


Maackiain (DL-Maackiain) is isolated from Maackia amurensis Rupr.et Maxim. Maackiain (DL-Maackiain) is a larvicidal agent against Aedes aegypti mosquito.xp Parasitol with a LD50 of ?21.95 μg/mL[1]. Maackiain (DL-Maackiain) induces fragmentations of DNA to oligonucleosomal-sized fragments that like a characteristic of apoptosis in the HL-60 cells[2]. Maackiain (DL-Maackiain) is isolated from Maackia amurensis Rupr.et Maxim. Maackiain (DL-Maackiain) is a larvicidal agent against Aedes aegypti mosquito.xp Parasitol with a LD50 of ?21.95 μg/mL[1]. Maackiain (DL-Maackiain) induces fragmentations of DNA to oligonucleosomal-sized fragments that like a characteristic of apoptosis in the HL-60 cells[2].

   

isolonchocarpin

isolonchocarpin

C20H18O3 (306.1256)


   

(1r,9s,10s)-5,9,14-trimethoxy-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11,13,15-hexaene

(1r,9s,10s)-5,9,14-trimethoxy-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11,13,15-hexaene

C18H18O5 (314.1154)


   

6-methoxy-8,8-dimethyl-2-phenylpyrano[2,3-h]chromen-4-one

6-methoxy-8,8-dimethyl-2-phenylpyrano[2,3-h]chromen-4-one

C21H18O4 (334.1205)


   

(2s)-5,7-dihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-en-1-yl)phenyl]-8-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

(2s)-5,7-dihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-en-1-yl)phenyl]-8-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

C30H36O5 (476.2563)


   

(2r,3r)-3,7-dihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-en-1-yl)phenyl]-8-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

(2r,3r)-3,7-dihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-en-1-yl)phenyl]-8-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

C30H36O5 (476.2563)


   

2,7,15-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁶,²¹]henicosa-1(13),3(11),4(8),5,9,16,18,20-octaen-12-one

2,7,15-trioxapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁶,²¹]henicosa-1(13),3(11),4(8),5,9,16,18,20-octaen-12-one

C18H10O4 (290.0579)


   

(2e)-1-(4-hydroxy-1-benzofuran-5-yl)-3-phenylprop-2-en-1-one

(2e)-1-(4-hydroxy-1-benzofuran-5-yl)-3-phenylprop-2-en-1-one

C17H12O3 (264.0786)


   

6'-demethoxypraecansone b

6'-demethoxypraecansone b

C21H20O4 (336.1362)


   

(2z)-3-hydroxy-1-(4-methoxy-1-benzothiophen-5-yl)-3-phenylprop-2-en-1-one

(2z)-3-hydroxy-1-(4-methoxy-1-benzothiophen-5-yl)-3-phenylprop-2-en-1-one

C18H14O3S (310.0664)


   

2'-methoxylupalbigenin

2'-methoxylupalbigenin

C26H28O6 (436.1886)


   

(3r)-1-(4-methoxy-1-benzofuran-5-yl)-3-phenylpentan-1-one

(3r)-1-(4-methoxy-1-benzofuran-5-yl)-3-phenylpentan-1-one

C20H20O3 (308.1412)


   

3,7-dihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-en-1-yl)phenyl]-8-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

3,7-dihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-en-1-yl)phenyl]-8-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

C30H36O5 (476.2563)


   

(1s,12r,20s)-16,20-dimethoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13,15,17-hexaene

(1s,12r,20s)-16,20-dimethoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.0²,¹⁰.0⁴,⁸.0¹³,¹⁸]icosa-2,4(8),9,13,15,17-hexaene

C18H16O6 (328.0947)


   

7-hydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-en-1-yl)phenyl]-8-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

7-hydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-en-1-yl)phenyl]-8-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

C30H36O4 (460.2613)


   

6-hydroxy-8,8-dimethyl-2-phenylpyrano[2,3-f]chromen-4-one

6-hydroxy-8,8-dimethyl-2-phenylpyrano[2,3-f]chromen-4-one

C20H16O4 (320.1049)