FOH 8:0 (BioDeep_00000629771)
Secondary id: BioDeep_00000003253, BioDeep_00000004214, BioDeep_00000406241, BioDeep_00001867626, BioDeep_00001867656
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C8H18O (130.1357578)
中文名称: 4-甲基-2-庚醇, 2-辛醇, 仲辛醇, 6-甲基-3-庚醇, 正辛醇, 异辛醇
谱图信息:
最多检出来源 Chinese Herbal Medicine(otcml) 0.29%
分子结构信息
SMILES: C(O)C(CC)CCCC
InChI: InChI=1S/C8H18O/c1-2-3-4-5-6-7-8-9/h9H,2-8H2,1H3
描述信息
D012997 - Solvents
1-Octanol (Octanol), a saturated fatty alcohol, is a T-type calcium channels (T-channels) inhibitor with an IC50 of 4 μM for native T-currents[1]. 1-Octanol is a highly attractive biofuel with diesel-like properties[2].
1-Octanol (Octanol), a saturated fatty alcohol, is a T-type calcium channels (T-channels) inhibitor with an IC50 of 4 μM for native T-currents[1]. 1-Octanol is a highly attractive biofuel with diesel-like properties[2].
同义名列表
30 个代谢物同义名
xi-2-Ethyl-1-hexanol; 2-Ethylhexan-1-ol; 2-Ethylhexanol; FOH 8:0; 4-methyl-2-heptanol; 4-methylheptan-2-ol; Octan-2-ol; 2-OCTANOL; (S)-3-Octanol; octan-3-ol; (2xi,4xi)-2,4-Dimethyl-1-hexanol; 2,4-dimethylhexan-1-ol; (2S)-2-octanol;(S)-(+)-2-octanol;(S)-2-octanol;d-octan-2-ol; (2S)-octan-2-ol; (2R)-2-octanol;(R)-(-)-2-octanol;(R)-2-octanol;l-octan-2-ol; (2R)-octan-2-ol; Octan-3S-ol; Octan-3R-ol; 6-Methylheptan-3-ol; 6-methyl-3-heptanol; 3-Methylheptan-2-ol; 2-Methylheptan-4R-ol; (3S,4S)-4-Methylheptan-3-ol; 4S-Methylheptan-3S-ol; (3R,4S)-4-Methylheptan-3-ol; 4S-Methylheptan-3R-ol; Octan-1-ol; n-octanol; 1-octanol; Octanol
数据库引用编号
60 个数据库交叉引用编号
- ChEBI: CHEBI:16011
- ChEBI: CHEBI:165509
- ChEBI: CHEBI:37869
- ChEBI: CHEBI:186745
- ChEBI: CHEBI:137757
- ChEBI: CHEBI:16188
- KEGG: C02498
- KEGG: C00756
- PubChem: 7720
- PubChem: 143345
- PubChem: 20083
- PubChem: 14753148
- PubChem: 6999002
- PubChem: 445789
- PubChem: 86783
- PubChem: 35784
- PubChem: 12650794
- PubChem: 6993196
- PubChem: 6993195
- PubChem: 957
- DrugBank: DB12452
- ChEMBL: CHEMBL31637
- ChEMBL: CHEMBL510068
- ChEMBL: CHEMBL26215
- LipidMAPS: LMFA05000703
- LipidMAPS: LMFA05000630
- LipidMAPS: LMFA05000620
- LipidMAPS: LMFA05000568
- LipidMAPS: LMFA05000553
- LipidMAPS: LMFA05000551
- LipidMAPS: LMFA05000547
- LipidMAPS: LMFA05000492
- LipidMAPS: LMFA05000490
- LipidMAPS: LMFA05000482
- LipidMAPS: LMFA05000479
- LipidMAPS: LMFA05000476
- LipidMAPS: LMFA05000473
- LipidMAPS: LMFA05000472
- LipidMAPS: LMFA05000130
- MeSH: 1-Octanol
- CAS: 104-76-7
- CAS: 56298-90-9
- CAS: 25339-16-6
- CAS: 4128-31-8
- CAS: 4128-32-9
- CAS: 123-96-6
- CAS: 3965-59-1
- CAS: 18720-66-6
- CAS: 67700-96-3
- CAS: 68603-15-6
- CAS: 111-87-5
- PubChem: 4018
- KNApSAcK: C00001264
- PDB-CCD: OC9
- 3DMET: B00168
- NIKKAJI: J2.459G
- PubChem: 5510
- NIKKAJI: J3.604H
- RefMet: n-Octanol
- medchemexpress: HY-W032013
分类词条
相关代谢途径
Reactome(0)
BioCyc(3)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
113 个相关的物种来源信息
- 3625 - Actinidia chinensis: 10.1021/JF00069A050
- 4681 - Allium ampeloprasum: 10.1080/10412905.1991.9697935
- 82210 - Allium grayi: 10.1271/BBB1961.52.2383
- 91198 - Allium macrostemon: 10.1271/BBB1961.52.2383
- 518704 - Alpinia chinensis: 10.1080/10412905.1994.9699357
- 299928 - Alpinia latilabris: 10.1080/10412905.1994.9698447
- 589713 - Anthemis aciphylla: 10.1248/CPB.54.222
- 3702 - Arabidopsis thaliana: 10.1111/TPJ.14311
- 72348 - Artemisia monosperma: 10.3109/13880209009082827
- 155124 - Aspalathus linearis: 10.1021/JF00062A024
- 5059 - Aspergillus flavus: 10.1016/J.PHYTOCHEM.2005.09.029
- 385370 - Aster scaber: 10.1021/JF00034A033
- 76974 - Atalantia buxifolia: 10.1080/10412905.1994.9698400
- 146531 - Avena byzantina: 10.1021/JF00112A045
- 4498 - Avena sativa: 10.1021/JF00112A045
- 28974 - Averrhoa carambola: 10.1021/JF00062A009
- 3589 - Basella alba: 10.1016/0889-1575(91)90017-Z
- 41492 - Bellis perennis: 10.1016/0031-9422(95)00183-8
- 173701 - Boswellia sacra: 10.1055/S-2006-962745
- 4442 - Camellia sinensis: 10.1021/JF00034A031
- 3483 - Cannabis sativa: 10.1021/NP50008A001
- 79829 - Capillipedium parviflorum: 10.1016/J.PHYTOCHEM.2004.04.003
- 114816 - Castanopsis cuspidata: 10.1021/JF60224A025
- 260595 - Cedronella canariensis: 10.1016/0031-9422(95)00241-X
- 114280 - Cichorium endivia: 10.1021/JF00068A014
- 3654 - Citrullus lanatus: 10.1271/BBB1961.49.3145
- 2706 - Citrus: 10.1080/10412905.1993.9698179
- 558547 - Citrus deliciosa:
- 79217 - Citrus iyo: 10.1271/BBB1961.47.1841
- 85571 - Citrus reticulata:
- 85571 - Citrus reticulata Blanco: -
- 37690 - Citrus trifoliata: 10.3390/MOLECULES13061333
- 55188 - Citrus unshiu:
- 4047 - Coriandrum sativum: 10.1021/JF00029A021
- 136209 - Curcuma aromatica: 10.1016/J.JPBA.2005.07.050
- 136221 - Curcuma wenyujin: 10.1016/J.JPBA.2005.07.050
- 329675 - Daphne odora: 10.1271/BBB1961.47.483
- 2715869 - Daphne papyracea: 10.1271/BBB1961.47.483
- 270439 - Erica manipuliflora: 10.1080/10412905.2000.9712044
- 102770 - Eupatorium cannabinum: 10.1055/S-2007-969599
- 52153 - Festuca rubra: 10.1016/0031-9422(91)84185-U
- 48119 - Glehnia littoralis: 10.1021/JF010219C
- 4397 - Hamamelis virginiana: 10.1055/S-2006-957420
- 261800 - Helichrysum pendulum: 10.1055/S-2006-957552
- 360619 - Heracleum antasiaticum: 10.1080/10412905.1993.9698208
- 360621 - Heracleum persicum: 10.1055/S-2007-969621
- 185542 - Ilex paraguariensis: 10.1021/JF00025A023
- 16719 - Juglans nigra: 10.1080/10412905.1993.9698259
- 1231670 - Leiocarpa semicalva: 10.1055/S-2006-957552
- 5353 - Lentinula edodes:
- 4606 - Lolium arundinaceum: 10.1016/0031-9422(91)84185-U
- 105884 - Lonicera japonica: 10.1186/1471-2164-13-195
- 3750 - Malus domestica: 10.1002/FOOD.19810250610
- 283210 - Malus pumila: 10.1002/FOOD.19810250610
- 389206 - Mandragora autumnalis: 10.1080/10412905.1998.9700991
- 33117 - Mandragora officinarum: 10.1080/10412905.1998.9700991
- 3879 - Medicago sativa: 10.1016/S0031-9422(97)00119-2
- 38859 - Mentha longifolia: 10.1080/10412905.1991.9697909
- 29719 - Mentha spicata: 10.1080/10412905.1991.9697909
- 39350 - Ocimum basilicum: 10.1080/10412905.1995.9698501
- 84561 - Oecophylla smaragdina: 10.1271/BBB1961.54.3335
- 4146 - Olea europaea: 10.1016/S0031-9422(97)00730-9
- 145953 - Ophrys sphegodes: 10.1016/S0031-9422(00)81276-5
- 371859 - Opuntia ficus-indica: 10.1021/JF60218A053
- 1268187 - Origanum cordifolium: 10.1016/0378-8741(91)90063-J
- 39352 - Origanum vulgare: 10.1080/10412905.1993.9698253
- 1477654 - Pectis elongata var. floribunda: 10.1080/10412905.1999.9701062
- 158596 - Pelargonium endlicherianum: 10.1055/S-2006-960872
- 3435 - Persea americana: 10.1021/JF00019A020
- 3885 - Phaseolus vulgaris: 10.1021/JF60199A053
- 3528 - Phytolacca acinosa: 10.1007/S10600-019-02670-2
- 260139 - Pimenta racemosa: 10.1080/10412905.1995.9698553
- 204156 - Platostoma africanum: 10.1055/S-2006-962093
- 204187 - Plectranthus glabratus: 10.1080/10412905.1993.9698226
- 5322 - Pleurotus ostreatus: 10.1021/JF960876I
- 62097 - Plumeria rubra: 10.1002/FFJ.2730070108
- 174549 - Polygala senega: 10.1002/FFJ.2730100408
- 3755 - Prunus dulcis: 10.1021/JF60228A025
- 120290 - Psidium guajava: 10.1016/0031-9422(82)80138-6
- 242839 - Rhodiola crenulata:
- 203015 - Rhodiola rosea: 10.1016/S0031-9422(02)00004-3
- 933131 - Salvia dorisiana:
- 39367 - Salvia rosmarinus: 10.1111/J.1365-2621.1985.TB10476.X
- 49988 - Satureja montana: 10.1080/10412905.1991.9700495
- 375857 - Scolochloa festucacea: 10.1016/0031-9422(91)84185-U
- 138013 - Senegalia berlandieri: 10.1021/JF00120A008
- 155234 - Sideritis athoa: 10.1080/10412905.1993.9698303
- 155260 - Sideritis romana: 10.1076/1388-0209(200004)3821-1FT106
- 155267 - Sideritis tragoriganum: 10.1016/S0031-9422(00)80325-8
- 265416 - Solanum stuckertii: 10.1080/10412905.1997.9700728
- 80338 - Spondias mombin: 10.1080/10412905.1992.9698127
- 547782 - Symphyotrichum undulatum: 10.1021/JF00034A033
- 169607 - Tagetes minuta:
- 58860 - Tamarindus indica: 10.1080/10412905.1990.9697860
- 88032 - Taxus canadensis: 10.1080/10412905.1993.9698163
- 155022 - Terminalia chebula: 10.4103/0974-8490.112421
- 1194133 - Thymus longicaulis:
- 1132412 - Thymus zygioides: 10.1080/10412905.1996.9701028
- 489417 - Tordylium apulum: 10.1080/10412905.1993.9698167
- 40145 - Tricholoma matsutake:
- 4565 - Triticum aestivum: 10.1016/S0031-9422(00)82634-5
- 13750 - Vaccinium macrocarpon: 10.3891/ACTA.CHEM.SCAND.21-2076
- 180772 - Vaccinium vitis-idaea: 10.3891/ACTA.CHEM.SCAND.21-0945
- 103349 - Vitis rotundifolia: 10.1021/JF00112A014
- 29760 - Vitis vinifera:
- 29760 - Vitis vinifera: 10.3389/FMICB.2017.00457
- 36659 - Volvariella volvacea: 10.1021/JF9703314
- 328402 - Zanthoxylum simulans: 10.1021/JF950577D
- 4577 - Zea mays:
- 136225 - Zingiber mioga: 10.1271/BBB1961.55.1655
- 94328 - Zingiber officinale:
- 94328 - Zingiber officinale: 10.1021/JF00097A027
- 94328 - Zingiber Officinale Roscoe: -
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
- Pierre-Alain van Griethuysen, Kelly R Redeker, Stuart A MacFarlane, Roy Neilson, Sue E Hartley. Virus-induced changes in root volatiles attract soil nematode vectors to infected plants.
The New phytologist.
2024 Mar; 241(5):2275-2286. doi:
10.1111/nph.19518
. [PMID: 38327027] - Qian Zhao, Jianmin Cao, Xianjie Cai, Jie Wang, Fanyu Kong, Dongkun Wang, Jing Wang. Antagonistic Activity of Volatile Organic Compounds Produced by Acid-Tolerant Pseudomonas protegens CLP-6 as Biological Fumigants To Control Tobacco Bacterial Wilt Caused by Ralstonia solanacearum.
Applied and environmental microbiology.
2023 Feb; ?(?):e0189222. doi:
10.1128/aem.01892-22
. [PMID: 36722969] - Wen Ouyang, Yaya Yu, Huajie Wang, Yongwen Jiang, Jinjie Hua, Jingming Ning, Haibo Yuan. Analysis of volatile metabolite variations in strip green tea during processing and effect of rubbing degree using untargeted and targeted metabolomics.
Food research international (Ottawa, Ont.).
2022 12; 162(Pt B):112099. doi:
10.1016/j.foodres.2022.112099
. [PMID: 36461339] - Ursula Perez-Salas, Lionel Porcar, Sumit Garg, Manuela A A Ayee, Irena Levitan. Effective Parameters Controlling Sterol Transfer: A Time-Resolved Small-Angle Neutron Scattering Study.
The Journal of membrane biology.
2022 10; 255(4-5):423-435. doi:
10.1007/s00232-022-00231-3
. [PMID: 35467109] - Rodrigo Maia de Pádua, Jadel Müller Kratz, Jennifer Munkert, Jéssica Wildgrube Bertol, Caroline Rigotto, Daniela Schuster, Vinícius Gonçalves Maltarollo, Wolfgang Kreis, Cláudia Maria Oliveira Simões, Fernão Castro Braga. Effects of Lipophilicity and Structural Features on the Antiherpes Activity of Digitalis Cardenolides and Derivatives.
Chemistry & biodiversity.
2022 Oct; 19(10):e202200411. doi:
10.1002/cbdv.202200411
. [PMID: 36085355] - Vivek Kempraj, Soo Jean Park, Donald N S Cameron, Phillip W Taylor. 1-Octanol emitted by Oecophylla smaragdina weaver ants repels and deters oviposition in Queensland fruit fly.
Scientific reports.
2022 09; 12(1):15768. doi:
10.1038/s41598-022-20102-0
. [PMID: 36130986] - Gang-Gang Chong, Liang-Yi Ding, Yan-Yan Qiu, Xiao-Long Qian, Ya-Li Dong, Chun-Xiu Li, Aitao Li, Jiang Pan, Jian-He Xu. Building Flexible Escherichia coli Modules for Bifunctionalizing n-Octanol: The Byproduct of Oleic Acid Biorefinery.
Journal of agricultural and food chemistry.
2022 Aug; 70(34):10543-10551. doi:
10.1021/acs.jafc.2c04329
. [PMID: 35997264] - Yu-Liang Qin, Shuai-Bing Zhang, Yang-Yong Lv, Huan-Chen Zhai, Yuan-Sen Hu, Jing-Ping Cai. The antifungal mechanisms of plant volatile compound 1-octanol against Aspergillus flavus growth.
Applied microbiology and biotechnology.
2022 Jul; ?(?):. doi:
10.1007/s00253-022-12049-z
. [PMID: 35779097] - Richard Wibel, Patrick Knoll, Bao Le-Vinh, Gergely Kali, Andreas Bernkop-Schnürch. Synthesis and evaluation of sulfosuccinate-based surfactants as counterions for hydrophobic ion pairing.
Acta biomaterialia.
2022 05; 144(?):54-66. doi:
10.1016/j.actbio.2022.03.013
. [PMID: 35292415] - Anh T Ngoc Do, Yoonsub Kim, Yeonjeong Ha, Jung-Hwan Kwon. Estimating the Bioaccumulation Potential of Hydrophobic Ultraviolet Stabilizers Using Experimental Partitioning Properties.
International journal of environmental research and public health.
2022 03; 19(7):. doi:
10.3390/ijerph19073989
. [PMID: 35409673] - Takanari Wakayama, Yuki Ito, Mio Miyake, Karin Nomasa, Kiyoshi Sakai, Naoko Oya, Hirotaka Sato, Hiroyuki Ohno, Michihiro Kamijima. Inhalation exposure to 2-ethyl-1-hexanol causes hepatomegaly and transient lipid accumulation without induction of peroxisome proliferator-activated receptor alpha in mice.
Industrial health.
2021 Nov; 59(6):383-392. doi:
10.2486/indhealth.2020-0252
. [PMID: 34588381] - Nam Ah Kim, Hyun Woo Yu, Ga Yeon Noh, Sang-Koo Park, Wonku Kang, Seong Hoon Jeong. Protein microbeadification to achieve highly concentrated protein formulation with reversible properties and in vivo pharmacokinetics after reconstitution.
International journal of biological macromolecules.
2021 Aug; 185(?):935-948. doi:
10.1016/j.ijbiomac.2021.07.012
. [PMID: 34237365] - Ian Sofian Yunus, Zhixuan Wang, Pachara Sattayawat, Jonathan Muller, Fessehaye W Zemichael, Klaus Hellgardt, Patrik R Jones. Improved Bioproduction of 1-Octanol Using Engineered Synechocystis sp. PCC 6803.
ACS synthetic biology.
2021 06; 10(6):1417-1428. doi:
10.1021/acssynbio.1c00029
. [PMID: 34003632] - Christopher M Ranger, Marek Dzurenko, Jenny Barnett, Ruchika Geedi, Louela Castrillo, Matthew Ethington, Matthew Ginzel, Karla Addesso, Michael E Reding. Electrophysiological and Behavioral Responses of an Ambrosia Beetle to Volatiles of its Nutritional Fungal Symbiont.
Journal of chemical ecology.
2021 May; 47(4-5):463-475. doi:
10.1007/s10886-021-01263-0
. [PMID: 33761047] - David R Hall, Steven J Harte, Daniel P Bray, Dudley I Farman, Rob James, Celine X Silva, Michelle T Fountain. Hero Turned Villain: Identification of Components of the Sex Pheromone of the Tomato Bug, Nesidiocoris tenuis.
Journal of chemical ecology.
2021 May; 47(4-5):394-405. doi:
10.1007/s10886-021-01270-1
. [PMID: 33844148] - Poovarasan Neelakandan, Chiu-Chung Young, Asif Hameed, Yu-Ning Wang, Kui-Nuo Chen, Fo-Ting Shen. Volatile 1-octanol of tea (Camellia sinensis L.) fuels cell division and indole-3-acetic acid production in phylloplane isolate Pseudomonas sp. NEEL19.
Scientific reports.
2021 02; 11(1):2788. doi:
10.1038/s41598-021-82442-7
. [PMID: 33531600] - Sascha R A Alles, Max A Odem, Van B Lu, Ryan M Cassidy, Peter A Smith. Chronic BDNF simultaneously inhibits and unmasks superficial dorsal horn neuronal activity.
Scientific reports.
2021 01; 11(1):2249. doi:
10.1038/s41598-021-81269-6
. [PMID: 33500423] - Delin Sun, Thasin A Peyear, W F Drew Bennett, Matthew Holcomb, Stewart He, Fangqiang Zhu, Felice C Lightstone, Olaf S Andersen, Helgi I Ingólfsson. Assessing the Perturbing Effects of Drugs on Lipid Bilayers Using Gramicidin Channel-Based In Silico and In Vitro Assays.
Journal of medicinal chemistry.
2020 10; 63(20):11809-11818. doi:
10.1021/acs.jmedchem.0c00958
. [PMID: 32945672] - Néstor J Hernández Lozada, Trevor R Simmons, Ke Xu, Michael A Jindra, Brian F Pfleger. Production of 1-octanol in Escherichia coli by a high flux thioesterase route.
Metabolic engineering.
2020 09; 61(?):352-359. doi:
10.1016/j.ymben.2020.07.004
. [PMID: 32707169] - Taísa Busaranho Franchin, Bruna Cristina Ulian Silva, Rone Aparecido DeGrandis, Michelle Fidelis Corrêa, Cecília Maria Simões de Queiroz Aranha, Joáo Paulo S Fernandes, Michel Leandro Campos, Rosângela Gonçalves Peccinini. Assessment of the Physicochemical Properties and Stability for Pharmacokinetic Prediction of Pyrazinoic Acid Derivatives.
Current drug metabolism.
2020; 21(9):714-721. doi:
10.2174/1389200221666200907145722
. [PMID: 32895039] - Nazanin Pirooznia, Khosrou Abdi, Davood Beiki, Farshad Emami, Seyed Shahriar Arab, Omid Sabzevari, Zahra Pakdin-Parizi, Parham Geramifar. Radiosynthesis, Biological Evaluation, and Preclinical Study of a 68Ga-Labeled Cyclic RGD Peptide as an Early Diagnostic Agent for Overexpressed α v β 3 Integrin Receptors in Non-Small-Cell Lung Cancer.
Contrast media & molecular imaging.
2020; 2020(?):8421657. doi:
10.1155/2020/8421657
. [PMID: 32292304] - Xiaofei Han, Juan Chen, Hongdeng Qiu, Yan-Ping Shi. Solid/liquid phase microextraction of five bisphenol-type endocrine disrupting chemicals by using a hollow fiber reinforced with graphene oxide nanoribbons, and determination by HPLC-PDA.
Mikrochimica acta.
2019 05; 186(6):375. doi:
10.1007/s00604-019-3498-2
. [PMID: 31127364] - Saied Saeed Hosseiny Davarani, Ahmad Pourahadi, Peivand Ghasemzadeh. Quantification of controlled release leuprolide and triptorelin in rabbit plasma using electromembrane extraction coupled with HPLC-UV.
Electrophoresis.
2019 04; 40(7):1074-1081. doi:
10.1002/elps.201800481
. [PMID: 30653693] - Chan Wu, Yang Zhang, Daoqiu Yang, Jinfeng Zhang, Juanjuan Ma, Dan Cheng, Jianming Chen, Li Deng. Novel SN38 derivative-based liposome as anticancer prodrug: an in vitro and in vivo study.
International journal of nanomedicine.
2019; 14(?):75-85. doi:
10.2147/ijn.s187906
. [PMID: 30587986] - Atyeh Rahimi, Saeed Nojavan. Electromembrane extraction of verapamil and riluzole from urine and wastewater samples using a mixture of organic solvents as a supported liquid membrane: Study on electric current variations.
Journal of separation science.
2019 Jan; 42(2):566-573. doi:
10.1002/jssc.201800741
. [PMID: 30371989] - Timothy R Fennell, James M Mathews, Rodney W Snyder, Yan Hong, Scott L Watson, Sherry R Black, Barry S McIntyre, Suramya Waidyanatha. Metabolism and disposition of 2-ethylhexyl-p-methoxycinnamate following oral gavage and dermal exposure in Harlan Sprague Dawley rats and B6C3F1/N mice and in hepatocytes in vitro.
Xenobiotica; the fate of foreign compounds in biological systems.
2018 Nov; 48(11):1142-1156. doi:
10.1080/00498254.2017.1400129
. [PMID: 29111853] - G Ermondi, M Vallaro, M P Camacho-Leal, T Potter, S Visentin, G Caron. Charged cyclic hexapeptides: Updating molecular descriptors for permeability purposes.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
2018 Sep; 122(?):85-93. doi:
10.1016/j.ejps.2018.06.021
. [PMID: 29935350] - Yvonne Connolly Martin. How medicinal chemists learned about log P.
Journal of computer-aided molecular design.
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