(-)-beta-Phellandrene (BioDeep_00000014760)
Secondary id: BioDeep_00000624507, BioDeep_00000859506, BioDeep_00001872140
human metabolite PANOMIX_OTCML-2023 Endogenous natural product
代谢物信息卡片
化学式: C10H16 (136.1252)
中文名称:
谱图信息:
最多检出来源 Homo sapiens(feces) 14.88%
分子结构信息
SMILES: C1=C[C@@H](CCC1=C)C(C)C
InChI: InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,6,8,10H,3,5,7H2,1-2H3/t10-/m0/s1
描述信息
(-)-beta-Phellandrene is found in pine nut. Phellandrene is the name for a pair of organic compounds that have a similar molecular structure and similar chemical properties. alpha-Phellandrene and beta-phellandrene are cyclic monoterpenes and are double-bond isomers. The phellandrenes are used in fragrances because of their pleasing aromas. (Wikipedia).
同义名列表
22 个代谢物同义名
(6R)-3-methylidene-6-(propan-2-yl)cyclohex-1-ene; (6R)-3-Methylene-6-(1-methylethyl)cyclohexene; (-)-3-Methylene-6-(1-methylethyl)cyclohexene; 3-methylene-6-(1-methylethyl)cyclohexene; (3R)-3-Isopropyl-6-methylenecyclohexene; (R)-3-Isopropyl-6-methylenecyclohexene; 4-Isopropyl-1-methylene-2-cyclohexene; 3-Isopropyl-6-methylene-1-cyclohexene; (-)-p-Mentha-1(7),2-diene; beta-Phellandrene L-form; (±)-beta-phellandrene; Β-phellandrene L-form; p-Mentha-1(7),2-diene; b-Phellandrene L-form; (-)-beta-Phellandrene; L-beta-Phellandrene; (-)-b-Phellandrene; (±)-β-phellandrene; (-)-Β-phellandrene; Beta-Phellandrene; L-Β-phellandrene; (-)-beta-Phellandrene
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
14 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(2)
- oleoresin monoterpene volatiles biosynthesis:
geranyl diphosphate ⟶ β-myrcene + diphosphate
- superpathway of oleoresin turpentine biosynthesis:
(2E,6E)-farnesyl diphosphate ⟶ (E)-α-bisabolene + diphosphate
WikiPathways(0)
Plant Reactome(3)
- Metabolism and regulation:
ATP + CoA + propionate ⟶ AMP + PPi + PROP-CoA
- Secondary metabolism:
GPP + H2O ⟶ PPi + geraniol
- Oleoresin monoterpene volatiles biosynthesis:
GPP ⟶ (+)-3-carene + PPi
INOH(0)
PlantCyc(9)
- trichome monoterpenes biosynthesis:
neryl diphosphate ⟶ α-phellandrene + diphosphate
- trichome monoterpenes biosynthesis:
neryl diphosphate ⟶ α-phellandrene + diphosphate
- trichome monoterpenes biosynthesis:
neryl diphosphate ⟶ β-phellandrene + diphosphate
- oleoresin monoterpene volatiles biosynthesis:
geranyl diphosphate ⟶ β-myrcene + diphosphate
- superpathway of oleoresin turpentine biosynthesis:
(2E,6E)-farnesyl diphosphate ⟶ (E)-α-bisabolene + diphosphate
- trichome monoterpenes biosynthesis:
neryl diphosphate ⟶ α-phellandrene + diphosphate
- trichome monoterpenes biosynthesis:
neryl diphosphate ⟶ α-phellandrene + diphosphate
- trichome monoterpenes biosynthesis:
neryl diphosphate ⟶ α-phellandrene + diphosphate
- trichome monoterpenes biosynthesis:
neryl diphosphate ⟶ α-phellandrene + diphosphate
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
77 个相关的物种来源信息
- 3319 - Abies: LTS0063520
- 45372 - Abies alba: 10.1002/JPS.3080220408
- 45372 - Abies alba: LTS0063520
- 97175 - Abies procera: 10.1002/JPS.3080220408
- 97175 - Abies procera: LTS0063520
- 4011 - Anacardiaceae: LTS0063520
- 99027 - Anthemis: LTS0063520
- 589713 - Anthemis aciphylla: 10.1248/CPB.54.222
- 589713 - Anthemis aciphylla: LTS0063520
- 4890 - Ascomycota: LTS0063520
- 1131492 - Aspergillaceae: LTS0063520
- 5052 - Aspergillus: LTS0063520
- 41067 - Aspergillus candidus: 10.1016/S0045-6535(99)00015-6
- 41067 - Aspergillus candidus: LTS0063520
- 4210 - Asteraceae: LTS0063520
- 4200 - Caprifoliaceae: LTS0063520
- 3321 - Cedrus: LTS0063520
- 93692 - Cedrus libani: 10.1016/J.PHYMED.2007.03.013
- 93692 - Cedrus libani: LTS0063520
- 558547 - Citrus deliciosa: 10.3390/MOLECULES21060814
- 37334 - Citrus maxima: 10.3390/MOLECULES21060814
- 171251 - Citrus medica: 10.3390/MOLECULES21060814
- 85571 - Citrus reticulata: 10.3390/MOLECULES21060814
- 237574 - Citrus sunki: 10.3390/MOLECULES21060814
- 37690 - Citrus trifoliata: 10.3390/MOLECULES21060814
- 3781 - Crassulaceae: LTS0063520
- 3932 - Eucalyptus: LTS0063520
- 1711222 - Eucalyptus cneorifolia: 10.1039/JR9370000986
- 1711222 - Eucalyptus cneorifolia: LTS0063520
- 2759 - Eukaryota: LTS0063520
- 147545 - Eurotiomycetes: LTS0063520
- 4751 - Fungi: LTS0063520
- 9606 - Homo sapiens: -
- 186771 - Jungermanniopsida: LTS0063520
- 4136 - Lamiaceae: LTS0063520
- 3398 - Magnoliopsida: LTS0063520
- 3195 - Marchantiophyta: LTS0063520
- 3931 - Myrtaceae: LTS0063520
- 3328 - Picea: LTS0063520
- 3329 - Picea abies: 10.1016/0031-9422(93)85508-O
- 3329 - Picea abies: LTS0063520
- 3332 - Picea sitchensis: 10.1002/JPS.3080200111
- 3332 - Picea sitchensis: LTS0063520
- 3318 - Pinaceae: LTS0063520
- 58019 - Pinopsida: LTS0063520
- 3337 - Pinus: LTS0063520
- 3345 - Pinus monticola: 10.1002/JPS.3080191108
- 3345 - Pinus monticola: LTS0063520
- 13215 - Piper: LTS0063520
- 130381 - Piper arboreum: 10.1016/S0031-9422(97)00762-0
- 130381 - Piper arboreum: LTS0063520
- 425151 - Piper fimbriulatum: 10.1016/S0031-9422(97)00762-0
- 425151 - Piper fimbriulatum: LTS0063520
- 13216 - Piper nigrum: 10.3390/MOLECULES24234244
- 16739 - Piperaceae: LTS0063520
- 53018 - Plagiochila: LTS0063520
- 173485 - Plagiochila rutilans: LTS0063520
- 283744 - Plagiochila rutilans var. standleyi: 10.1016/S0031-9422(01)00056-5
- 283744 - Plagiochila rutilans var. standleyi: LTS0063520
- 53016 - Plagiochilaceae: LTS0063520
- 202994 - Rhodiola: LTS0063520
- 203015 - Rhodiola rosea: 10.1016/S0031-9422(02)00004-3
- 203015 - Rhodiola rosea: LTS0063520
- 43850 - Schinus: 10.1016/S0031-9422(00)94384-X
- 43850 - Schinus: LTS0063520
- 155231 - Sideritis: LTS0063520
- 35493 - Streptophyta: LTS0063520
- 58023 - Tracheophyta: LTS0063520
- 28568 - Trichocomaceae: LTS0063520
- 3358 - Tsuga: LTS0063520
- 3359 - Tsuga heterophylla: 10.1002/JPS.3080191208
- 3359 - Tsuga heterophylla: LTS0063520
- 19952 - Valeriana: LTS0063520
- 19953 - Valeriana officinalis: 10.1135/CCCC19661113
- 19953 - Valeriana officinalis: LTS0063520
- 19944 - Valerianaceae: LTS0063520
- 33090 - Viridiplantae: LTS0063520
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。
亚细胞结构定位 | 关联基因列表 |
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文献列表
- J Bohlmann, M Phillips, V Ramachandiran, S Katoh, R Croteau. cDNA cloning, characterization, and functional expression of four new monoterpene synthase members of the Tpsd gene family from grand fir (Abies grandis).
Archives of biochemistry and biophysics.
1999 Aug; 368(2):232-43. doi:
10.1006/abbi.1999.1332
. [PMID: 10441373]