NCBI Taxonomy: 38413

Eragrostis (ncbi_taxid: 38413)

found 30 associated metabolites at genus taxonomy rank level.

Ancestor: Eragrostidinae

Child Taxonomies: Eragrostis curvula, Eragrostis tef, Eragrostis capensis, Eragrostis japonica, Eragrostis plana, Eragrostis nigra, Eragrostis minor, Eragrostis densa, Eragrostis lurida, Eragrostis patens, Eragrostis obtusa, Eragrostis aspera, Eragrostis pilosa, Eragrostis lugens, Eragrostis porosa, Eragrostis neesii, Eragrostis nutans, Eragrostis fallax, Eragrostis cilianensis, Eragrostis fractus, Eragrostis nevinii, Eragrostis bicolor, Eragrostis pilgeri, Eragrostis grandis, Eragrostis braunii, Eragrostis stapfii, Eragrostis wiseana, Eragrostis hirsuta, Eragrostis biflora, Eragrostis superba, Eragrostis frankii, Eragrostis confusa, Eragrostis tenella, Eragrostis rotifer, Eragrostis papposa, Eragrostis falcata, Eragrostis tremula, Eragrostis angusta, Eragrostis reptans, Eragrostis brownii, Eragrostis lanipes, Eragrostis lappula, Eragrostis mollior, Eragrostis dielsii, Eragrostis palmeri, Eragrostis plumbea, Eragrostis hispida, Eragrostis pusilla, Eragrostis viscosa, Eragrostis baileyi, Eragrostis scabrida, Eragrostis albensis, Eragrostis eriopoda, Eragrostis abortiva, Eragrostis imberbis, Eragrostis squamata, Eragrostis racemosa, Eragrostis ciliaris, Eragrostis mexicana, Eragrostis cumingii, Eragrostis elongata, Eragrostis rigidior, Eragrostis andicola, Eragrostis truncata, Eragrostis congesta, Eragrostis cubensis, Eragrostis airoides, Eragrostis floccosa, Eragrostis olivacea, Eragrostis leporina, Eragrostis refracta, Eragrostis sabulosa, Eragrostis speciosa, Eragrostis rufinerva, Eragrostis kennedyae, Eragrostis nigricans, Eragrostis trichodes, Eragrostis amurensis, Eragrostis nindensis, Eragrostis kiwuensis, Eragrostis schultzii, Eragrostis schimperi, Eragrostis elliottii, Eragrostis botryodes, Eragrostis bahiensis, Eragrostis gummiflua, Eragrostis macilenta, Eragrostis laniflora, Eragrostis setifolia, Eragrostis tenellula, Eragrostis hypnoides, Eragrostis xerophila, Eragrostis basedowii, Eragrostis boinensis, Eragrostis canescens, Eragrostis capuronii, Eragrostis dentifera, Eragrostis gangetica, Eragrostis humbertii, Eragrostis homomalla, Eragrostis lacunaria, Eragrostis monticola, Eragrostis peruviana, Eragrostis rufescens, Eragrostis prolifera, Eragrostis pseudopoa, Eragrostis pubescens, Eragrostis scaligera, Eragrostis attenuata, Eragrostis virginica, Eragrostis perennans, Eragrostis autumnalis, Eragrostis ferruginea, Eragrostis exasperata, Eragrostis humidicola, Eragrostis cylindrica, Eragrostis unioloides, Eragrostis desertorum, Eragrostis lanicaulis, Eragrostis parviflora, Eragrostis pastoensis, Eragrostis soratensis, Eragrostis suaveolens, Eragrostis orcuttiana, Eragrostis tenuiflora, Eragrostis barrelieri, Eragrostis chapelieri, Eragrostis heteromera, Eragrostis intermedia, Eragrostis polytricha, Eragrostis lasioclada, Eragrostis acutiflora, Eragrostis aegyptiaca, Eragrostis leptocarpa, Eragrostis articulata, Eragrostis tenuifolia, Eragrostis filicaulis, Eragrostis lateritica, Eragrostis interrupta, Eragrostis capillaris, Eragrostis aethiopica, Eragrostis pilgeriana, Eragrostis chabouisii, Eragrostis variabilis, Eragrostis subsecunda, Eragrostis sarmentosa, Eragrostis pectinacea, Eragrostis atrovirens, Eragrostis setulifera, Eragrostis trichocolea, Eragrostis multicaulis, Eragrostis pergracilis, Eragrostis obtusiflora, Eragrostis namaquensis, Eragrostis weberbaueri, Eragrostis lehmanniana, Eragrostis trichophora, Eragrostis atropioides, Eragrostis chalarantha, Eragrostis contrerasii, Eragrostis hirticaulis, Eragrostis maypurensis, Eragrostis planiculmis, Eragrostis potamophila, Eragrostis stolonifera, Eragrostis pseudobtusa, Eragrostis scotelliana, Eragrostis spectabilis, Eragrostis trachycarpa, Eragrostis agrostoides, Eragrostis chloromelas, Eragrostis sessilispica, Eragrostis australasica, Eragrostis leptostachya, Eragrostis paniciformis, Eragrostis secundiflora, Eragrostis crassinervis, unclassified Eragrostis, Eragrostis patentissima, Eragrostis betsileensis, Eragrostis scopelophila, Eragrostis spartinoides, Eragrostis lilliputiana, Eragrostis nightingaleae, Eragrostis harpachnoides, Eragrostis cylindriflora, Eragrostis crateriformis, Eragrostis patentipilosa, Eragrostis elegantissima, Eragrostis confertiflora, Eragrostis hildebrandtii, Eragrostis echinochloidea, Eragrostis schweinfurthii, Eragrostis x pseudo-obtusa, Eragrostis curtipedicellata, Eragrostis cf. bemarivensis JH-2017

Naringenin

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-, (2S)-

C15H12O5 (272.0685)


Naringenin is a flavorless, colorless flavanone, a type of flavonoid. It is the predominant flavanone in grapefruit, and is found in a variety of fruits and herbs. Naringenin has the skeleton structure of a flavanone with three hydroxy groups at the 4, 5, and 7 carbons. It may be found both in the aglycol form, naringenin, or in its glycosidic form, naringin, which has the addition of the disaccharide neohesperidose attached via a glycosidic linkage at carbon 7. Naringenin (not to be confused with naringin) is a flavanone that is considered to have a bioactive effect on human health as antioxidant, free radical scavenger, antiinflammatory, carbohydrate metabolism promoter, immunity system modulater. This substance has also been shown to repair DNA. Scientists exposed cells to 80 micomoles of naringenin per liter, for 24 hours, and found that the amount of hydroxyl damage to the DNA was reduced by 24 percent in that very short period of time. Unfortunately, this bioflavonoid is difficult to absorb on oral ingestion. Only 15\\\\\\\% of ingested naringenin will get absorbed, in the human gastrointestinal tract, in the best case scenario. A full glass of orange juice will supply about enough naringenin to achieve a concentration of about 0.5 micromoles per liter. Naringenin is a biomarker for the consumption of citrus fruits. (S)-naringenin is the (S)-enantiomer of naringenin. It has a role as an expectorant and a plant metabolite. It is a naringenin and a (2S)-flavan-4-one. It is a conjugate acid of a (S)-naringenin(1-). It is an enantiomer of a (R)-naringenin. Naringenin is a natural product found in Elaeodendron croceum, Garcinia multiflora, and other organisms with data available. See also: Naringin (related). Most widely distributed flavanone. Citrus fruits (grapefruit, oranges and pummelos) are especially good sources. Glycosides also widely distributed The (S)-enantiomer of naringenin. [Raw Data] CB070_Naringenin_pos_20eV_CB000030.txt [Raw Data] CB070_Naringenin_pos_10eV_CB000030.txt [Raw Data] CB070_Naringenin_pos_40eV_CB000030.txt [Raw Data] CB070_Naringenin_pos_30eV_CB000030.txt [Raw Data] CB070_Naringenin_pos_50eV_CB000030.txt [Raw Data] CB070_Naringenin_neg_10eV_000021.txt [Raw Data] CB070_Naringenin_neg_30eV_000021.txt [Raw Data] CB070_Naringenin_neg_50eV_000021.txt [Raw Data] CB070_Naringenin_neg_20eV_000021.txt [Raw Data] CB070_Naringenin_neg_40eV_000021.txt (±)-Naringenin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=67604-48-2 (retrieved 2024-07-09) (CAS RN: 67604-48-2). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity.

   

Lupeol

(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol

C30H50O (426.3861)


Lupeol is a pentacyclic triterpenoid that is lupane in which the hydrogen at the 3beta position is substituted by a hydroxy group. It occurs in the skin of lupin seeds, as well as in the latex of fig trees and of rubber plants. It is also found in many edible fruits and vegetables. It has a role as an anti-inflammatory drug and a plant metabolite. It is a secondary alcohol and a pentacyclic triterpenoid. It derives from a hydride of a lupane. Lupeol has been investigated for the treatment of Acne. Lupeol is a natural product found in Ficus auriculata, Ficus septica, and other organisms with data available. See also: Calendula Officinalis Flower (part of). A pentacyclic triterpenoid that is lupane in which the hydrogen at the 3beta position is substituted by a hydroxy group. It occurs in the skin of lupin seeds, as well as in the latex of fig trees and of rubber plants. It is also found in many edible fruits and vegetables. D000893 - Anti-Inflammatory Agents Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic?triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent?androgen receptor (AR)?inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC)[1]. Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic?triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent?androgen receptor (AR)?inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC)[1].

   

Amyrin

(3S,4aR,5R,6aR,6bR,8S,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-eicosahydro-picen-3-ol

C30H50O (426.3861)


Beta-amyrin is a pentacyclic triterpenoid that is oleanane substituted at the 3beta-position by a hydroxy group and containing a double bond between positions 12 and 13. It is one of the most commonly occurring triterpenoids in higher plants. It has a role as a plant metabolite and an Aspergillus metabolite. It is a pentacyclic triterpenoid and a secondary alcohol. It derives from a hydride of an oleanane. beta-Amyrin is a natural product found in Ficus pertusa, Ficus septica, and other organisms with data available. See also: Calendula Officinalis Flower (part of); Viburnum opulus bark (part of); Centaurium erythraea whole (part of). A pentacyclic triterpenoid that is oleanane substituted at the 3beta-position by a hydroxy group and containing a double bond between positions 12 and 13. It is one of the most commonly occurring triterpenoids in higher plants. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1]. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1].

   

Naringenin

5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O5 (272.0685)


Naringenin is a trihydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5, 6 and 4. It is a trihydroxyflavanone and a member of 4-hydroxyflavanones. 5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one is a natural product found in Prunus mume, Helichrysum cephaloideum, and other organisms with data available. D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006727 - Hormone Antagonists > D004965 - Estrogen Antagonists A trihydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5, 6 and 4. D005765 - Gastrointestinal Agents > D000897 - Anti-Ulcer Agents (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity.

   

beta-Amyrin

4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-ol

C30H50O (426.3861)


Beta-amryin, also known as B-amryin, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Beta-amryin is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Beta-amryin can be found in pigeon pea, which makes beta-amryin a potential biomarker for the consumption of this food product.

   

Isosakuranetin 7-O-rhamnoside

5,7-Dihydroxy-4-methoxyflavanone 7-O-rhamnoside

C22H24O9 (432.142)


   

β-Amyrin

beta-amyrin-H2O

C30H50O (426.3861)


Beta-amyrin, also known as amyrin or (3beta)-olean-12-en-3-ol, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Thus, beta-amyrin is considered to be an isoprenoid lipid molecule. Beta-amyrin is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Beta-amyrin can be synthesized from oleanane. Beta-amyrin is also a parent compound for other transformation products, including but not limited to, erythrodiol, glycyrrhetaldehyde, and 24-hydroxy-beta-amyrin. Beta-amyrin can be found in a number of food items such as thistle, pepper (c. baccatum), wakame, and endive, which makes beta-amyrin a potential biomarker for the consumption of these food products. The amyrins are three closely related natural chemical compounds of the triterpene class. They are designated α-amyrin (ursane skeleton), β-amyrin (oleanane skeleton) and δ-amyrin. Each is a pentacyclic triterpenol with the chemical formula C30H50O. They are widely distributed in nature and have been isolated from a variety of plant sources such as epicuticular wax. In plant biosynthesis, α-amyrin is the precursor of ursolic acid and β-amyrin is the precursor of oleanolic acid. All three amyrins occur in the surface wax of tomato fruit. α-Amyrin is found in dandelion coffee . β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1]. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1].

   

Naringenin

(2S) -2,3-Dihydro-5,7-dihydroxy-2- (4-hydroxyphenyl) -4H-1-benzopyran-4-one

C15H12O5 (272.0685)


Annotation level-1 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.904 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.906 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.901 CONFIDENCE standard compound; ML_ID 50 (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity.

   

lupeol

Lup-20(29)-en-3.beta.-ol

C30H50O (426.3861)


D000893 - Anti-Inflammatory Agents Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic?triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent?androgen receptor (AR)?inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC)[1]. Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic?triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent?androgen receptor (AR)?inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC)[1].

   

Asahina

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-, (2S)-

C15H12O5 (272.0685)


D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006727 - Hormone Antagonists > D004965 - Estrogen Antagonists D005765 - Gastrointestinal Agents > D000897 - Anti-Ulcer Agents (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes[1]. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity. Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity.

   

4a,7,7,10a-tetramethyl-octahydro-1h-naphtho[2,1-b]pyran-3-one

4a,7,7,10a-tetramethyl-octahydro-1h-naphtho[2,1-b]pyran-3-one

C17H28O2 (264.2089)


   

(3r,4s,5s,6r)-2-{[(3s,4ar,6as,6br,8ar,14as,14br)-4,4,4a,6a,6b,8a,11,11,14a,14b-decamethyl-tetradecahydropicen-3-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl acetate

(3r,4s,5s,6r)-2-{[(3s,4ar,6as,6br,8ar,14as,14br)-4,4,4a,6a,6b,8a,11,11,14a,14b-decamethyl-tetradecahydropicen-3-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl acetate

C40H68O7 (660.4965)


   

(12e,14e)-tritriaconta-12,14-diene

(12e,14e)-tritriaconta-12,14-diene

C33H64 (460.5008)


   

(6ar,8as,12as,12br)-6a,9,9,12a-tetramethyl-dodecahydronaphtho[2,1-b]oxocine

(6ar,8as,12as,12br)-6a,9,9,12a-tetramethyl-dodecahydronaphtho[2,1-b]oxocine

C19H34O (278.261)


   

{6a,9,9,12a-tetramethyl-dodecahydronaphtho[2,1-b]oxocin-3-yl}methyl acetate

{6a,9,9,12a-tetramethyl-dodecahydronaphtho[2,1-b]oxocin-3-yl}methyl acetate

C22H38O3 (350.2821)


   

(3r,6ar,8as,12as,12br)-6a,9,9,12a-tetramethyl-dodecahydronaphtho[2,1-b]oxocine-3-carboxylic acid

(3r,6ar,8as,12as,12br)-6a,9,9,12a-tetramethyl-dodecahydronaphtho[2,1-b]oxocine-3-carboxylic acid

C20H34O3 (322.2508)


   

5-hydroxy-7-methoxy-2-(3-methoxy-4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-2,3-dihydro-1-benzopyran-4-one

5-hydroxy-7-methoxy-2-(3-methoxy-4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-2,3-dihydro-1-benzopyran-4-one

C23H26O11 (478.1475)


   

6a,9,9,12a-tetramethyl-dodecahydronaphtho[2,1-b]oxocine-3-carboxylic acid

6a,9,9,12a-tetramethyl-dodecahydronaphtho[2,1-b]oxocine-3-carboxylic acid

C20H34O3 (322.2508)


   

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-4-one

C28H32O16 (624.169)


   

6a,9,9,12a-tetramethyl-dodecahydronaphtho[2,1-b]oxocine

6a,9,9,12a-tetramethyl-dodecahydronaphtho[2,1-b]oxocine

C19H34O (278.261)


   

[(3r,6ar,8as,12as,12br)-6a,9,9,12a-tetramethyl-dodecahydronaphtho[2,1-b]oxocin-3-yl]methyl acetate

[(3r,6ar,8as,12as,12br)-6a,9,9,12a-tetramethyl-dodecahydronaphtho[2,1-b]oxocin-3-yl]methyl acetate

C22H38O3 (350.2821)


   

(6ar,8as,12as,12br)-6a,9,9,12a-tetramethyl-decahydro-1h-naphtho[2,1-b]oxocin-3-one

(6ar,8as,12as,12br)-6a,9,9,12a-tetramethyl-decahydro-1h-naphtho[2,1-b]oxocin-3-one

C19H32O2 (292.2402)


   

ambreinolide

ambreinolide

C17H28O2 (264.2089)


   

6a,9,9,12a-tetramethyl-decahydro-1h-naphtho[2,1-b]oxocin-3-one

6a,9,9,12a-tetramethyl-decahydro-1h-naphtho[2,1-b]oxocin-3-one

C19H32O2 (292.2402)


   

tritriaconta-12,14-dien-5-ol

tritriaconta-12,14-dien-5-ol

C33H64O (476.4957)


   

tritriaconta-12,14-diene

tritriaconta-12,14-diene

C33H64 (460.5008)


   

tritriaconta-12,14-dien-5-one

tritriaconta-12,14-dien-5-one

C33H62O (474.48)


   

(12e,14e)-tritriaconta-12,14-dien-5-one

(12e,14e)-tritriaconta-12,14-dien-5-one

C33H62O (474.48)


   

(5s,12e,14e)-tritriaconta-12,14-dien-5-ol

(5s,12e,14e)-tritriaconta-12,14-dien-5-ol

C33H64O (476.4957)


   

(3r,4ar,6ar,6bs,8ar,12ar,14ar,14br)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol

(3r,4ar,6ar,6bs,8ar,12ar,14ar,14br)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol

C30H50O (426.3861)