NCBI Taxonomy: 2067815

Commiphora mukul (ncbi_taxid: 2067815)

found 70 associated metabolites at species taxonomy rank level.

Ancestor: Commiphora

Child Taxonomies: none taxonomy data.

Neocembrene

1,5,9-Cyclotetradecatriene, 1,5,9-trimethyl-12-(1-methylethenyl)-

C20H32 (272.2503872)


   

Cembrene

(1E,3Z,6E,10E,14S)-3,7,11-Trimethyl-14-(1-methylethyl)-1,3,6,10-cyclotetradecatetraene

C20H32 (272.2503872)


Cembrene is found in fats and oils. Cembrene is a constituent of oil of Pinus koraiensis (Korean pine) Cembrene A, or sometimes neocembrene, is a natural monocyclic diterpene isolated from corals of the genus Nephthea. It is a colorless oil with a faint wax-like odor.

   

Isogermafurene

6-ethenyl-3,6-dimethyl-5-(prop-1-en-2-yl)-4,5,6,7-tetrahydro-1-benzofuran

C15H20O (216.151407)


Isogermafurene is found in herbs and spices. Isogermafurene is isolated from Curcuma zedoaria (zedoary), present to some extent in nearly all Curcuma species. Isolated from Curcuma zedoaria (zedoary), present to some extent in nearly all Curcuma subspecies Isogermafurene is found in herbs and spices. Curzerene is a natural product found in Commiphora myrrha and Lindera pulcherrima var. hemsleyana with data available.

   

Guggulsterone

(8R,9S,10R,13S,14S,17Z)-17-ethylidene-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15-decahydrocyclopenta[a]phenanthrene-3,16-dione

C21H28O2 (312.2089188)


Guggulsterone is a 3-hydroxy steroid. It has a role as an androgen. Guggulsterone is a natural product found in Commiphora mukul and Commiphora wightii with data available. E-Guggulsterone is a 3-hydroxy steroid. It has a role as an androgen. E-Guggulsterone is a natural product found in Commiphora mukul and Commiphora wightii with data available. (-)-(E)-Guggulsterone is the metabolite of Z-guggulsterone. Guggulsterone is an active constituent of guggulipid, an ayurvedic agent derived from Commiphora mukul. Guggulsterone has hypolipidaemic activity[1]. (-)-(E)-Guggulsterone is the metabolite of Z-guggulsterone. Guggulsterone is an active constituent of guggulipid, an ayurvedic agent derived from Commiphora mukul. Guggulsterone has hypolipidaemic activity[1]. (Z)-Guggulsterone, a constituent of Indian Ayurvedic medicinal plant Commiphora mukul, inhibits the growth of human prostate cancer cells by causing apoptosis. (Z)-Guggulsterone inhibits angiogenesis by suppressing the VEGF–VEGF-R2–Akt signaling axis[1]. (Z)-Guggulsterone is also a potent FXR antagonist. (Z)-Guggulsterone reduces ACE2 expression and SARS-CoV-2 infection[2]. (Z)-Guggulsterone, a constituent of Indian Ayurvedic medicinal plant Commiphora mukul, inhibits the growth of human prostate cancer cells by causing apoptosis. (Z)-Guggulsterone inhibits angiogenesis by suppressing the VEGF–VEGF-R2–Akt signaling axis[1]. (Z)-Guggulsterone is also a potent FXR antagonist. (Z)-Guggulsterone reduces ACE2 expression and SARS-CoV-2 infection[2]. Guggulsterone is a plant sterol derived from the gum resin of the tree Commiphora wightii. Guggulsterone inhibits the growth of a wide variety of tumor cells and induces apoptosis through down regulation of antiapoptotic gene products (IAP1, xIAP, Bfl-1/A1, Bcl-2, cFLIP and survivin), modulation of cell cycle proteins (cyclin D1 and c-Myc), activation of caspases and JNK, inhibition of Akt[1]. Guggulsterone, a farnesoid X receptor (FXR) antagonist, decreases CDCA-induced FXR activation with IC50s of 17 and 15 μM for Z- and E-Guggulsterone, respectively[2]. Guggulsterone is a plant sterol derived from the gum resin of the tree Commiphora wightii. Guggulsterone inhibits the growth of a wide variety of tumor cells and induces apoptosis through down regulation of antiapoptotic gene products (IAP1, xIAP, Bfl-1/A1, Bcl-2, cFLIP and survivin), modulation of cell cycle proteins (cyclin D1 and c-Myc), activation of caspases and JNK, inhibition of Akt[1]. Guggulsterone, a farnesoid X receptor (FXR) antagonist, decreases CDCA-induced FXR activation with IC50s of 17 and 15 μM for Z- and E-Guggulsterone, respectively[2]. Guggulsterone is a plant sterol derived from the gum resin of the tree Commiphora wightii. Guggulsterone inhibits the growth of a wide variety of tumor cells and induces apoptosis through down regulation of antiapoptotic gene products (IAP1, xIAP, Bfl-1/A1, Bcl-2, cFLIP and survivin), modulation of cell cycle proteins (cyclin D1 and c-Myc), activation of caspases and JNK, inhibition of Akt[1]. Guggulsterone, a farnesoid X receptor (FXR) antagonist, decreases CDCA-induced FXR activation with IC50s of 17 and 15 μM for Z- and E-Guggulsterone, respectively[2].

   
   

Curzerene

6-ethenyl-3,6-dimethyl-5-(prop-1-en-2-yl)-4,5,6,7-tetrahydro-1-benzofuran

C15H20O (216.151407)


   

guggulsterone

(8R,9S,10R,13S,14S,17E)-17-ethylidene-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15-decahydrocyclopenta[a]phenanthrene-3,16-quinone

C21H28O2 (312.2089188)


(-)-(E)-Guggulsterone is the metabolite of Z-guggulsterone. Guggulsterone is an active constituent of guggulipid, an ayurvedic agent derived from Commiphora mukul. Guggulsterone has hypolipidaemic activity[1]. (-)-(E)-Guggulsterone is the metabolite of Z-guggulsterone. Guggulsterone is an active constituent of guggulipid, an ayurvedic agent derived from Commiphora mukul. Guggulsterone has hypolipidaemic activity[1]. Guggulsterone is a plant sterol derived from the gum resin of the tree Commiphora wightii. Guggulsterone inhibits the growth of a wide variety of tumor cells and induces apoptosis through down regulation of antiapoptotic gene products (IAP1, xIAP, Bfl-1/A1, Bcl-2, cFLIP and survivin), modulation of cell cycle proteins (cyclin D1 and c-Myc), activation of caspases and JNK, inhibition of Akt[1]. Guggulsterone, a farnesoid X receptor (FXR) antagonist, decreases CDCA-induced FXR activation with IC50s of 17 and 15 μM for Z- and E-Guggulsterone, respectively[2]. Guggulsterone is a plant sterol derived from the gum resin of the tree Commiphora wightii. Guggulsterone inhibits the growth of a wide variety of tumor cells and induces apoptosis through down regulation of antiapoptotic gene products (IAP1, xIAP, Bfl-1/A1, Bcl-2, cFLIP and survivin), modulation of cell cycle proteins (cyclin D1 and c-Myc), activation of caspases and JNK, inhibition of Akt[1]. Guggulsterone, a farnesoid X receptor (FXR) antagonist, decreases CDCA-induced FXR activation with IC50s of 17 and 15 μM for Z- and E-Guggulsterone, respectively[2]. Guggulsterone is a plant sterol derived from the gum resin of the tree Commiphora wightii. Guggulsterone inhibits the growth of a wide variety of tumor cells and induces apoptosis through down regulation of antiapoptotic gene products (IAP1, xIAP, Bfl-1/A1, Bcl-2, cFLIP and survivin), modulation of cell cycle proteins (cyclin D1 and c-Myc), activation of caspases and JNK, inhibition of Akt[1]. Guggulsterone, a farnesoid X receptor (FXR) antagonist, decreases CDCA-induced FXR activation with IC50s of 17 and 15 μM for Z- and E-Guggulsterone, respectively[2].

   

Cembrene

(+)-Thunbergen

C20H32 (272.2503872)


   

(1e,3z,6e,10z)-14-isopropyl-3,7,11-trimethylcyclotetradeca-1,3,6,10-tetraene

(1e,3z,6e,10z)-14-isopropyl-3,7,11-trimethylcyclotetradeca-1,3,6,10-tetraene

C20H32 (272.2503872)


   

14-isopropyl-3,7,11-trimethylcyclotetradeca-2,6,10-trien-1-ol

14-isopropyl-3,7,11-trimethylcyclotetradeca-2,6,10-trien-1-ol

C20H34O (290.2609514)


   

(4as,5r,6r,8as)-6-hydroxy-5-[(3e,7e,11e)-13-hydroxy-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-1,1,4a,6-tetramethyl-hexahydronaphthalen-2-one

(4as,5r,6r,8as)-6-hydroxy-5-[(3e,7e,11e)-13-hydroxy-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-1,1,4a,6-tetramethyl-hexahydronaphthalen-2-one

C30H50O3 (458.37597500000004)


   

(1s,2z,4e,7e,11e)-1-isopropyl-4,8,12-trimethylcyclotetradeca-2,4,7,11-tetraen-1-ol

(1s,2z,4e,7e,11e)-1-isopropyl-4,8,12-trimethylcyclotetradeca-2,4,7,11-tetraen-1-ol

C20H32O (288.24530219999997)


   

(1s,2e,6e,10e,14s)-14-isopropyl-3,7,11-trimethylcyclotetradeca-2,6,10-trien-1-ol

(1s,2e,6e,10e,14s)-14-isopropyl-3,7,11-trimethylcyclotetradeca-2,6,10-trien-1-ol

C20H34O (290.2609514)


   

(1e,3as,3bs,9ar,9br,11ar)-1-ethylidene-9a,11a-dimethyl-3h,3ah,3bh,4h,5h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-2,7-dione

(1e,3as,3bs,9ar,9br,11ar)-1-ethylidene-9a,11a-dimethyl-3h,3ah,3bh,4h,5h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-2,7-dione

C21H28O2 (312.2089188)


   

(2e,6e,10e)-13-[(1r,2r,4as,8as)-2-hydroxy-2,5,5,8a-tetramethyl-6-oxo-hexahydronaphthalen-1-yl]-2,6,10-trimethyltrideca-2,6,10-trienoic acid

(2e,6e,10e)-13-[(1r,2r,4as,8as)-2-hydroxy-2,5,5,8a-tetramethyl-6-oxo-hexahydronaphthalen-1-yl]-2,6,10-trimethyltrideca-2,6,10-trienoic acid

C30H48O4 (472.3552408)


   

2-methoxy-8-[2-(4-methoxyphenyl)-hexahydrofuro[2,3-c]furan-6-yl]-4,6,10,12-tetraoxatricyclo[7.3.0.0³,⁷]dodeca-1,3(7),8-triene

2-methoxy-8-[2-(4-methoxyphenyl)-hexahydrofuro[2,3-c]furan-6-yl]-4,6,10,12-tetraoxatricyclo[7.3.0.0³,⁷]dodeca-1,3(7),8-triene

C22H22O8 (414.1314612)


   

(5s,6s)-6-ethenyl-3,6-dimethyl-5-(prop-1-en-2-yl)-5,7-dihydro-4h-1-benzofuran

(5s,6s)-6-ethenyl-3,6-dimethyl-5-(prop-1-en-2-yl)-5,7-dihydro-4h-1-benzofuran

C15H20O (216.151407)


   

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

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

C27H46O3 (418.34467659999996)


   

(1r,3ar,4r,6ar)-1,4-bis(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan

(1r,3ar,4r,6ar)-1,4-bis(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan

C24H30O8 (446.194058)


   

3,8a-dimethyl-5-methylidene-4h,4ah,6h,9h-naphtho[2,3-b]furan

3,8a-dimethyl-5-methylidene-4h,4ah,6h,9h-naphtho[2,3-b]furan

C15H18O (214.1357578)


   

(4as,8as)-3,8a-dimethyl-5-methylidene-4h,4ah,6h,9h-naphtho[2,3-b]furan

(4as,8as)-3,8a-dimethyl-5-methylidene-4h,4ah,6h,9h-naphtho[2,3-b]furan

C15H18O (214.1357578)


   

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

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

C27H46O3 (418.34467659999996)


   

(5s,6s)-6-ethenyl-3,6-dimethyl-5-(prop-1-en-2-yl)-5,7-dihydro-1-benzofuran-4-one

(5s,6s)-6-ethenyl-3,6-dimethyl-5-(prop-1-en-2-yl)-5,7-dihydro-1-benzofuran-4-one

C15H18O2 (230.1306728)


   

2-[(2r,3as,6s,6as)-2-(4-methoxyphenyl)-hexahydrofuro[2,3-c]furan-6-yl]-8-methoxy-4,6,10,12-tetraoxatricyclo[7.3.0.0³,⁷]dodeca-1,3(7),8-triene

2-[(2r,3as,6s,6as)-2-(4-methoxyphenyl)-hexahydrofuro[2,3-c]furan-6-yl]-8-methoxy-4,6,10,12-tetraoxatricyclo[7.3.0.0³,⁷]dodeca-1,3(7),8-triene

C22H22O8 (414.1314612)


   

(2e,6e,10e)-13-[(1r,2r,4as,6s,8as)-2,6-dihydroxy-2,5,5,8a-tetramethyl-hexahydro-1h-naphthalen-1-yl]-2,6,10-trimethyltrideca-2,6,10-trienoic acid

(2e,6e,10e)-13-[(1r,2r,4as,6s,8as)-2,6-dihydroxy-2,5,5,8a-tetramethyl-hexahydro-1h-naphthalen-1-yl]-2,6,10-trimethyltrideca-2,6,10-trienoic acid

C30H50O4 (474.37089000000003)


   

2,3,4-trihydroxyicosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

2,3,4-trihydroxyicosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C30H50O7 (522.355635)


   

(3z,6z,10z)-14-isopropyl-3,7,11-trimethylcyclotetradeca-1,3,6,10-tetraene

(3z,6z,10z)-14-isopropyl-3,7,11-trimethylcyclotetradeca-1,3,6,10-tetraene

C20H32 (272.2503872)


   

(2s,3s,4r)-2,3,4-trihydroxyicosyl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

(2s,3s,4r)-2,3,4-trihydroxyicosyl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C30H50O7 (522.355635)