24-Methylenecycloartan-3-ol (BioDeep_00000006999)
Secondary id: BioDeep_00000019561, BioDeep_00000637027, BioDeep_00001868795
human metabolite PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C31H52O (440.4018)
中文名称: 24-亚甲基环阿屯醇
谱图信息:
最多检出来源 Homo sapiens(plant) 16.91%
分子结构信息
SMILES: C1[C@@H](C([C@H]2[C@]3(C1)[C@]1([C@@H](CC2)[C@]2([C@](CC1)([C@H](CC2)[C@@H](CCC(=C)C(C)C)C)C)C)C3)(C)C)O
InChI: InChI=1S/C31H52O/c1-20(2)21(3)9-10-22(4)23-13-15-29(8)25-12-11-24-27(5,6)26(32)14-16-30(24)19-31(25,30)18-17-28(23,29)7/h20,22-26,32H,3,9-19H2,1-2,4-8H3/t22-,23-,24+,25+,26+,28-,29+,30-,31+/m1/s1
描述信息
24-methylenecycloartan-3-ol belongs to cycloartanols and derivatives class of compounds. Those are steroids containing a cycloartanol moiety. 24-methylenecycloartan-3-ol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 24-methylenecycloartan-3-ol can be found in a number of food items such as oregon yampah, common persimmon, pineapple, and climbing bean, which makes 24-methylenecycloartan-3-ol a potential biomarker for the consumption of these food products.
同义名列表
32 个代谢物同义名
(1S,3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methyl-5-methylideneheptan-2-yl]pentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-ol; 4alpha,4beta,14alpha-Trimethyl-9beta,19-cyclo-5alpha-ergost-24(24(1))-en-3beta-ol; 4Α,4β,14α-trimethyl-9β,19-cyclo-5α-ergost-24(24(1))-en-3β-ol; 4a,4b,14a-Trimethyl-9b,19-cyclo-5a-ergost-24(24(1))-en-3b-ol; 9,19-Cyclolanostan-3-o1, 24-methylene-, (3β)-; (3beta,9beta)-24-Methylene-9,19-cyclolanostan-3-ol; 24-methylene-9beta,19-cyclo-lanostan-3beta-ol; (3Β,9β)-24-methylene-9,19-cyclolanostan-3-ol; (3b,9b)-24-Methylene-9,19-cyclolanostan-3-ol; (3beta)-24-Methylene-9,19-cyclolanostan-3-ol; (3β)-24-Methylene-9,19-cyclolanostan-3-ol; 9,19-Cyclo-24-methylenelanostan-3beta-ol; 24-Methylene-9,19-cyclolanostan-3beta-ol; 24-Methylene-9β,19-cyclo-lanostan-3β-ol; 24-Methylene-9b,19-cyclo-lanostan-3b-ol; 9,19-Cyclo-24-methylenelanostan-3β-ol; 3beta-Hydroxy-24-methylenecycloartane; 24-Methylene-9,19-cyclolanostan-3β-ol; 3β-Hydroxy-24-methylenecycloartane; 24-Methylenecycloartan-3beta-ol; 24-Methylencycloartan-3beta-ol; 24-Methylenecycloartan-3β-ol; 24-Methylenecycloartan-3b-ol; 24(28)-Methylenecycloartanol; 24-Methylencycloartan-3β-ol; 24-Methylenecycloartan-3-ol; 24-Methylidenecycloartanol; 24-methylene-cycloartanol; 24-Methylene cycloartanol; 24-methylenecycloartanol; 24-Methylenecycloartenol; 24-Methylidenecycloartanol
数据库引用编号
16 个数据库交叉引用编号
- ChEBI: CHEBI:1307
- KEGG: C08830
- PubChem: 94204
- HMDB: HMDB0303481
- Metlin: METLIN63310
- ChEMBL: CHEMBL376350
- MetaCyc: CPD-696
- KNApSAcK: C00003661
- foodb: FDB014438
- chemspider: 85017
- CAS: 1449-09-8
- PubChem: 11023
- LipidMAPS: LMST01100001
- 3DMET: B02440
- NIKKAJI: J113.713A
- KNApSAcK: 1307
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
24 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(24)
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
O2 + a reduced [NADPH-hemoprotein reductase] + sitosterol ⟶ H2O + an oxidized [NADPH-hemoprotein reductase] + stigmasterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
Δ24-25-sitosterol + H+ + NADPH ⟶ NADP+ + sitosterol
- phytosterol biosynthesis (plants):
4α-carboxy-4β,14α-dimethyl-9β,19-cyclo-5α-ergost-24(241)-en-3β-ol + NAD+ ⟶ CO2 + NADH + cycloeucalenone
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
118 个相关的物种来源信息
- 64042 - Actaea simplex: 10.1248/CPB.47.1157
- 338571 - Amaranthus blitum: 10.1016/S0031-9422(00)81167-X
- 3567 - Amaranthus caudatus: 10.1016/S0031-9422(00)81167-X
- 117272 - Amaranthus cruentus: 10.1016/S0031-9422(00)81167-X
- 3565 - Amaranthus hybridus: 10.1016/S0031-9422(00)81167-X
- 28502 - Amaranthus hypochondriacus: 10.1016/S0031-9422(00)81167-X
- 2613835 - Amaranthus leucocarpus: 10.1016/S0031-9422(00)81167-X
- 124763 - Amaranthus retroflexus: 10.1016/S0031-9422(00)81167-X
- 29722 - Amaranthus tricolor: 10.1016/S0031-9422(00)81167-X
- 180132 - Ammocharis coranica: 10.1016/S0031-9422(00)00039-X
- 1712201 - Archidendron chevalieri: 10.1055/S-2006-959392
- 4217 - Arctium lappa: 10.1016/S0031-9422(96)00343-3
- 146531 - Avena byzantina: 10.1016/S0031-9422(00)00062-5
- 4498 - Avena sativa: 10.1016/S0031-9422(00)00062-5
- 161934 - Beta vulgaris: 10.1016/S0031-9422(00)97034-1
- 3821 - Cajanus cajan: 10.1016/S0031-9422(00)94844-1
- 41496 - Calendula officinalis: 10.1016/S0031-9422(96)00343-3
- 4443 - Camellia japonica:
- 385388 - Camellia oleifera: 10.1248/CPB.45.2016
- 182300 - Camellia sasanqua: 10.1248/CPB.45.2016
- 4442 - Camellia sinensis: 10.1007/BF02534064
- 4222 - Carthamus tinctorius: 10.1016/S0031-9422(96)00343-3
- 46112 - Celosia argentea: 10.1016/S0031-9422(00)81167-X
- 3827 - Cicer arietinum: 10.1016/S0031-9422(00)94844-1
- 1329804 - Cirsium nipponicum: 10.1016/S0031-9422(96)00343-3
- 54228 - Clerodendrum splendens: 10.1016/S0031-9422(00)83192-1
- 51277 - Cosmos bipinnatus: 10.1016/S0031-9422(96)00343-3
- 2172426 - Costus tonkinensis: 10.1016/S0031-9422(97)00101-5
- 3656 - Cucumis melo: 10.1016/0031-9422(82)85222-9
- 4265 - Cynara cardunculus: 10.1016/S0031-9422(96)00343-3
- 397682 - Diplopterygium glaucum: 10.1248/CPB.41.624
- 1142948 - Dracaena cinnabari: 10.1016/0031-9422(94)00743-D
- 36777 - Elaeagnus angustifolia: 10.1007/BF02249647
- 509534 - Epidendrum fulgens: 10.1002/CHIN.199841193
- 34315 - Eucalyptus microcorys: 10.1016/S0031-9422(00)90191-2
- 1333886 - Euphorbia aleppica: 10.1016/0031-9422(95)00889-6
- 334664 - Euphorbia antiquorum: 10.1016/0031-9422(90)80134-3
- 1091613 - Euphorbia boetica: 10.1016/0031-9422(88)83136-4
- 38844 - Euphorbia cyparissias: 10.1055/S-2006-959586
- 526193 - Euphorbia ebracteolata: 10.1248/CPB.18.1276
- 3993 - Euphorbia esula: 10.1002/JPS.2600570604
- 1138347 - Euphorbia guyoniana: 10.1016/J.PHYTOCHEM.2007.01.017
- 756620 - Euphorbia heteradena: 10.1016/S0031-9422(99)00169-7
- 756622 - Euphorbia iberica: 10.1055/S-2006-960819
- 239687 - Euphorbia kansui: 10.1211/0022357001773607
- 1138348 - Euphorbia lactea: 10.4268/CJCMM20142015
- 212925 - Euphorbia lathyris: 10.3390/MOLECULES24234322
- 212941 - Euphorbia myrsinites: 10.1016/0031-9422(94)00806-5
- 1087772 - Euphorbia nicaeensis: 10.1055/S-2006-959736
- 1091639 - Euphorbia oxyphylla: 10.1016/S0031-9422(00)82286-4
- 38846 - Euphorbia peplus:
- 154995 - Euphorbia piscatoria: 10.1055/S-2006-959579
- 1091645 - Euphorbia retusa:
- 756632 - Euphorbia rigida: 10.1515/ZNB-1985-0420
- 38847 - Euphorbia segetalis: 10.1016/S0031-9422(97)01011-X
- 756633 - Euphorbia seguieriana: 10.1016/0031-9422(95)00514-8
- 1091647 - Euphorbia sulcata:
- 3494 - Ficus carica:
- 309341 - Ficus fistulosa: 10.1016/S0031-9422(98)00578-0
- 3274 - Gleichenia japonica: 10.1248/CPB.41.624
- 3847 - Glycine max: 10.1016/S0031-9422(00)94844-1
- 126678 - Goniophlebium formosanum: 10.1016/0031-9422(92)80289-Q
- 4232 - Helianthus annuus:
- 73282 - Helianthus debilis: 10.1016/S0031-9422(96)00343-3
- 193516 - Hippophae rhamnoides:
- 9606 - Homo sapiens: -
- 141487 - Hoya australis: 10.1055/S-0028-1097228
- 318058 - Ixeris chinensis: 10.1248/CPB.44.509
- 122810 - Lagerstroemia speciosa: 10.1080/10286020310001596024
- 123599 - Larix gmelinii: 10.1007/BF00574580
- 54800 - Larix kaempferi: 10.1016/S0031-9422(98)00302-1
- 3860 - Lathyrus sativus: 10.1016/S0031-9422(00)94844-1
- 3864 - Lens culinaris: 10.1016/S0031-9422(00)94844-1
- 73751 - Lophostemon confertus: 10.1071/CH9610471
- 29780 - Mangifera indica:
- 883867 - Matricaria discoidea: 10.1016/S0031-9422(96)00343-3
- 56017 - Matricaria matricarioides: 10.1016/S0031-9422(96)00343-3
- 155640 - Melia azedarach: 10.1055/S-0028-1097188
- 128655 - Neolitsea sericea: 10.1016/0031-9422(92)83139-P
- 4097 - Nicotiana tabacum: 10.1007/BF02660305
- 555479 - Nigella sativa: 10.1016/0031-9422(86)88046-3
- 4146 - Olea europaea: 10.1007/BF02541591
- 200954 - Ononis natrix:
- 4530 - Oryza sativa:
- 40708 - Paeonia emodi: 10.1007/BF02679791
- 4054 - Panax ginseng: 10.1007/BF02645749
- 44588 - Panax quinquefolius:
- 1035881 - Pandanus boninensis: 10.1016/J.PHYTOCHEM.2005.08.019
- 3527 - Phytolacca americana: 10.1007/BF02534064
- 3888 - Pisum sativum: 10.1016/S0031-9422(00)94844-1
- 3693 - Populus tremuloides: 10.1139/V63-343
- 3240 - Psilotum nudum: 10.1007/BF02637687
- 49215 - Salvia nemorosa: 10.1016/S0031-9422(00)90672-1
- 4202 - Sambucus nigra:
- 1383557 - Scutellaria discolor: 10.1248/CPB.44.1540
- 300844 - Sesamum alatum: 10.1002/JSFA.2740590309
- 4182 - Sesamum indicum: 10.1002/JSFA.2740590309
- 300843 - Sesamum radiatum: 10.1002/JSFA.2740590309
- 403019 - Sideritis discolor: 10.1016/J.PHYTOCHEM.2009.05.011
- 92921 - Silybum marianum: 10.1016/S0031-9422(96)00343-3
- 4111 - Solanum melongena: 10.1007/BF02537347
- 35871 - Sparganium eurycarpum: 10.1007/S12272-010-0404-1
- 203643 - Sparganium stoloniferum: 10.1007/S12272-010-0404-1
- 41788 - Stauntonia hexaphylla: 10.1021/NP50063A024
- 13702 - Symphoricarpos albus: 10.1016/S0031-9422(00)80074-6
- 50225 - Taraxacum officinale: 10.1016/S0031-9422(96)00343-3
- 170727 - Taraxacum platycarpum: 10.1016/S0031-9422(96)00343-3
- 588385 - Tillandsia recurvata: 10.1021/NP50126A020
- 49541 - Tillandsia usneoides: 10.1021/NP960075+
- 1640458 - Trichilia claussenii: 10.1016/0031-9422(95)00969-8
- 3116 - Ulva intestinalis: 10.1016/S0031-9422(00)82185-8
- 63410 - Ulva lactuca: 10.1016/S0031-9422(00)82185-8
- 23278 - Vahlia capensis: 10.1016/0031-9422(94)00710-B
- 3914 - Vigna angularis: 10.1271/NOGEIKAGAKU1924.59.895
- 3915 - Vigna mungo: 10.1016/S0031-9422(00)94844-1
- 99658 - Xanthoceras sorbifolium: 10.1021/NP9902441
- 69721 - Zantedeschia aethiopica: 10.1016/S0031-9422(98)00092-2
- 4577 - Zea mays: 10.1016/0031-9422(84)83081-2
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Vanessa Suaza-Gaviria, Ana María Mesa-Vanegas, Omar Ocampo-Jiménez, Zulma Isabel Monsalve-Fonnegra. Antioxidant Activity and Phytopathogenic Control of Extracts and Fraction from Struthanthus calophyllus A.C.Sm. (Loranthaceae).
Chemistry & biodiversity.
2023 Feb; 20(2):e202200830. doi:
10.1002/cbdv.202200830
. [PMID: 36650106] - Fumiaki Okahara, Junko Suzuki, Kohjiro Hashizume, Noriko Osaki, Akira Shimotoyodome. Triterpene alcohols and sterols from rice bran reduce postprandial hyperglycemia in rodents and humans.
Molecular nutrition & food research.
2016 07; 60(7):1521-31. doi:
10.1002/mnfr.201500897
. [PMID: 26935127] - Faouzi Sakouhi, Christelle Absalon, Guido Flamini, Pier Luigi Cioni, Habib Kallel, Sadok Boukhchina. Lipid components of olive oil from Tunisian Cv. Sayali: characterization and authenticity.
Comptes rendus biologies.
2010 Sep; 333(9):642-8. doi:
10.1016/j.crvi.2010.05.001
. [PMID: 20816644] - Wahid Herchi, Saoussem Harrabi, Khaled Sebei, Sophie Rochut, Sadok Boukhchina, Claude Pepe, Habib Kallel. Phytosterols accumulation in the seeds of Linum usitatissimum L.
Plant physiology and biochemistry : PPB.
2009 Oct; 47(10):880-5. doi:
10.1016/j.plaphy.2009.07.001
. [PMID: 19616960] - Patricia Walter Rosa, Marina da Silva Machado, Fátima de Campos-Buzzi, Rivaldo Niero, Franco Delle Monache, Valdir Cechinel Filho. Seasonal and biological variations of Epidendrum mosenii: quantification of 24-methylenecycloartanol using gas chromatography.
Natural product research.
2007 Sep; 21(11):975-81. doi:
10.1080/14786410701371553
. [PMID: 17691046] - Shun Yao, Renming Liu, Xuefeng Huang, Lingyi Kong. Preparative isolation and purification of chemical constituents from the root of Adenophora tetraphlla by high-speed counter-current chromatography with evaporative light scattering detection.
Journal of chromatography. A.
2007 Jan; 1139(2):254-62. doi:
10.1016/j.chroma.2006.11.056
. [PMID: 17150224] - C Ma, N Nakamura, M Hattori, H Kakuda, J Qiao, H Yu. Inhibitory effects on HIV-1 protease of constituents from the wood of Xanthoceras sorbifolia.
Journal of natural products.
2000 Feb; 63(2):238-42. doi:
10.1021/np9902441
. [PMID: 10691716] - S Pascal, M Taton, A Rahier. Oxidative C4-demethylation of 24-methylene cycloartanol by a cyanide-sensitive enzymatic system from higher plant microsomes.
Biochemical and biophysical research communications.
1990 Oct; 172(1):98-106. doi:
10.1016/s0006-291x(05)80178-0
. [PMID: 2222486]