Daucosterol (BioDeep_00000343673)

Main id: BioDeep_00000000575

 

natural product PANOMIX_OTCML-2023


代谢物信息卡片


(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

化学式: C35H60O6 (576.439)
中文名称: β-Sitosterol β-D-glucoside, 西托糖苷, 胡萝卜甙, 胡萝卜苷
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C
InChI: InChI=1S/C35H60O6/c1-7-22(20(2)3)9-8-21(4)26-12-13-27-25-11-10-23-18-24(14-16-34(23,5)28(25)15-17-35(26,27)6)40-33-32(39)31(38)30(37)29(19-36)41-33/h10,20-22,24-33,36-39H,7-9,11-19H2,1-6H3/t21-,22-,24+,25+,26-,27+,28+,29-,30-,31+,32-,33-,34+,35-/m1/s1

描述信息

Daucosterol is a steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. It has a role as a plant metabolite. It is a steroid saponin, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a sitosterol. It derives from a hydride of a stigmastane.
Sitogluside is a natural product found in Ophiopogon intermedius, Ophiopogon jaburan, and other organisms with data available.
A steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa.
C308 - Immunotherapeutic Agent
Daucosterol is a natural sterol compound.
Daucosterol is a natural sterol compound.

同义名列表

75 个代谢物同义名

(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; (2R,3R,4S,5S,6R)-2-((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; (2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(1R,4R)-4-ethyl-1,5-dimethyl-hexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol; (2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol; BETA-SITOSTEROL GLUCOSIDE (DAUCOSTEROL) (CONSTITUENT OF STINGING NETTLE) [DSC]; BETA-SITOSTEROL GLUCOSIDE (DAUCOSTEROL) (CONSTITUENT OF STINGING NETTLE); .beta.-D-Glucopyranoside, (3.beta.)-stigmast-5-en-3-yl; Stigmast-5-ene, 3-beta-(beta-D-glucopyranosyloxy)-; beta-D-Glucopyranoside, (3beta)-stigmast-5-en-3-yl; 3.BETA.-(.BETA.-D-GLUCOPYRANOSYLOXY)STIGMAST-5-ENE; (3-beta)-Stigmast-5-en-3-yl-beta-D-glucopyranoside; (3beta)-stigmast-5-en-3-yl beta-D-glucopyranoside; 3-beta-(beta-D-Glucopyranosyloxy)stigmast-5-ene; 3beta-(beta-D-Glucopyranosyloxy)stigmast-5-ene; beta-sitosterol 3-O-beta-D-glucopyranoside; (-)-beta-Sitosterol-beta-D-glucopyranoside; Eleutheroside A;-Sitosterol -D-glucoside; SITOSTEROL 3-O-.BETA.-D-GLUCOPYRANOSIDE; beta-sitosteryl-beta-D-glucopyranoside; beta-sitosterol-beta-D-glucopyranoside; beta-sitosterol 3-O-beta-D-glucoside; .BETA.-SITOSTEROL-.BETA.-D-GLUCOSIDE; 3-O-beta-D-glucosyl-beta-sitosterol; beta-sitosterol-beta-D-glycoside; beta-Sitosterol beta-D-Glucoside; Sitosterol-3-O-beta-D-glucoside; beta-Sitosterol monoglucoside; sitosteryl 3-beta-D-glucoside; .beta.-sitosterol-glucoside; NPJICTMALKLTFW-OFUAXYCQSA-N; beta-sitosterol glucutonide; beta-Sitosterol D-glucoside; sitosterol beta-D-glucoside; b-Sitosterol b-D-glucoside; O-glucosyl-beta-sitosterol; beta-sitosterol glucoside; beta-SITOSTEROL-GLUCOSIDE; beta-Sitosteryl glucoside; Sitoglusido [INN-Spanish]; Sitoglusidum [INN-Latin]; sitosterol glucuronide; Sitogluside [USAN:INN]; Sitosterol D-glucoside; Sitogluside (USAN/INN); Sitosteryl glycoside; SITOGLUSIDE [USAN]; SITOGLUSIDE [INN]; beta-Daucosterol; UNII-U45VN859W3; eleutheroside A; Coriandrinol; Sitoglusidum; Daucosterine; Daucosterol; Sitoglusido; Sitogluside; Daucosterin; Alexandrin; U45VN859W3; Doursterol; lyoniside; AC1NX3NW; Sterolin; BSS-G; AW 10; AW-10; BSSG; (2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(1R,4R)-4-ethyl-1,5-dimethylhexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol; (2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(1R,4R)-4-ethyl-1,5-dimethyl-hexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-methylol-tetrahydropyran-3,4,5-triol; (2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methyl-heptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol; Sitogluside (USAN); AIDS-014857; AIDS014857; 474-58-8; D05848



数据库引用编号

16 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

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)

1103 个相关的物种来源信息

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
Cytoplasm 13 AKT1, ALB, BCL2, CASP3, CAT, G6PD, GPI, HPGDS, PIK3CA, SNCA, TH, TP53, VEGFA
Peripheral membrane protein 2 ACHE, G6PD
Endoplasmic reticulum membrane 2 BCL2, CD4
Nucleus 9 ACHE, AKT1, ALB, BCL2, CASP3, SNCA, TH, TP53, VEGFA
cytosol 13 AKT1, ALB, BCL2, CASP3, CAT, G6PD, GPI, GPT, HPGDS, PIK3CA, SNCA, TH, TP53
dendrite 1 TH
centrosome 2 ALB, TP53
nucleoplasm 4 AKT1, CASP3, HPGDS, TP53
Cell membrane 4 ACHE, AKT1, CD4, TNF
lamellipodium 2 AKT1, PIK3CA
Cell projection, axon 2 SNCA, TH
Synapse 2 ACHE, SNCA
cell cortex 2 AKT1, SNCA
cell surface 3 ACHE, TNF, VEGFA
glutamatergic synapse 2 AKT1, CASP3
Golgi apparatus 3 ACHE, ALB, VEGFA
Golgi membrane 1 INS
growth cone 1 SNCA
neuromuscular junction 1 ACHE
neuronal cell body 3 CASP3, SNCA, TNF
postsynapse 2 AKT1, SNCA
smooth endoplasmic reticulum 1 TH
synaptic vesicle 1 TH
Cytoplasm, cytosol 1 G6PD
Lysosome 1 SNCA
plasma membrane 6 ACHE, AKT1, CD4, PIK3CA, SNCA, TNF
synaptic vesicle membrane 1 SNCA
terminal bouton 1 TH
Membrane 9 ACHE, AKT1, BCL2, CAT, G6PD, GPI, SNCA, TP53, VEGFA
axon 2 SNCA, TH
extracellular exosome 5 ALB, CAT, G6PD, GPI, GPT
endoplasmic reticulum 4 ALB, BCL2, TP53, VEGFA
extracellular space 9 ACHE, ALB, GPI, IL2, IL4, INS, SNCA, TNF, VEGFA
perinuclear region of cytoplasm 4 ACHE, PIK3CA, SNCA, TH
adherens junction 1 VEGFA
intercalated disc 1 PIK3CA
mitochondrion 5 BCL2, CAT, SNCA, TH, TP53
protein-containing complex 6 AKT1, ALB, BCL2, CAT, SNCA, TP53
intracellular membrane-bounded organelle 3 CAT, G6PD, HPGDS
postsynaptic density 1 CASP3
Single-pass type I membrane protein 1 CD4
Secreted 8 ACHE, ALB, GPI, IL2, IL4, INS, SNCA, VEGFA
extracellular region 10 ACHE, ALB, CAT, GPI, IL2, IL4, INS, SNCA, TNF, VEGFA
cytoplasmic side of plasma membrane 2 G6PD, TH
Mitochondrion outer membrane 1 BCL2
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 1 BCL2
Mitochondrion matrix 1 TP53
mitochondrial matrix 2 CAT, TP53
Extracellular side 1 ACHE
anchoring junction 1 ALB
transcription regulator complex 1 TP53
centriolar satellite 1 G6PD
ciliary membrane 1 GPI
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 1 TP53
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 1 BCL2
external side of plasma membrane 2 CD4, TNF
Secreted, extracellular space, extracellular matrix 1 VEGFA
actin cytoskeleton 1 SNCA
perikaryon 1 TH
cytoplasmic vesicle 1 TH
microtubule cytoskeleton 1 AKT1
nucleolus 1 TP53
Melanosome membrane 1 TH
Early endosome 1 CD4
cell-cell junction 1 AKT1
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
vesicle 1 AKT1
Cytoplasm, perinuclear region 1 TH
Membrane raft 2 CD4, TNF
pore complex 1 BCL2
Cytoplasm, cytoskeleton 1 TP53
focal adhesion 1 CAT
spindle 1 AKT1
extracellular matrix 1 VEGFA
Peroxisome 1 CAT
basement membrane 1 ACHE
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
Nucleus, PML body 1 TP53
PML body 1 TP53
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 1 AKT1
secretory granule 1 VEGFA
neuron projection 1 TH
ciliary basal body 2 AKT1, ALB
chromatin 1 TP53
phagocytic cup 1 TNF
supramolecular fiber 1 SNCA
centriole 1 ALB
spindle pole 1 ALB
blood microparticle 1 ALB
Lipid-anchor, GPI-anchor 1 ACHE
site of double-strand break 1 TP53
endosome lumen 1 INS
side of membrane 1 ACHE
germ cell nucleus 1 TP53
replication fork 1 TP53
myelin sheath 1 BCL2
ficolin-1-rich granule lumen 2 CAT, GPI
secretory granule lumen 3 CAT, GPI, INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 3 ALB, CD4, INS
nuclear matrix 1 TP53
transcription repressor complex 1 TP53
platelet alpha granule lumen 2 ALB, VEGFA
axon terminus 1 SNCA
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
clathrin-coated endocytic vesicle membrane 1 CD4
[Isoform 1]: Nucleus 1 TP53
synaptic cleft 1 ACHE
death-inducing signaling complex 1 CASP3
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
T cell receptor complex 1 CD4
catalase complex 1 CAT
inclusion body 1 SNCA
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle 1 TH
BAD-BCL-2 complex 1 BCL2
[N-VEGF]: Cytoplasm 1 VEGFA
[VEGFA]: Secreted 1 VEGFA
[Isoform L-VEGF189]: Endoplasmic reticulum 1 VEGFA
[Isoform VEGF121]: Secreted 1 VEGFA
[Isoform VEGF165]: Secreted 1 VEGFA
VEGF-A complex 1 VEGFA
[Isoform H]: Cell membrane 1 ACHE
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA
ciliary transition fiber 1 ALB
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Sumin Lee, Jae-Hyun Kim, Minsun Kim, Sooyeon Hong, Hoyeon Park, Eom Ji Kim, Eun-Young Kim, Chungho Lee, Youngjoo Sohn, Hyuk Sang Jung. Exploring the Anti-Osteoporotic Potential of Daucosterol: Impact on Osteoclast and Osteoblast Activities. International journal of molecular sciences. 2023 Nov; 24(22):. doi: 10.3390/ijms242216465. [PMID: 38003654]
  • Feng Zhang, Mengyao Wang, Yang Zha, Jie Zhou, Jihong Han, Shuang Zhang. Daucosterol Alleviates Alcohol-Induced Hepatic Injury and Inflammation through P38/NF-κB/NLRP3 Inflammasome Pathway. Nutrients. 2023 Jan; 15(1):. doi: 10.3390/nu15010223. [PMID: 36615880]
  • Haoran Guo, Hongliang Zeng, Chuhan Fu, Jinhua Huang, Jianyun Lu, Yibo Hu, Ying Zhou, Liping Luo, Yushan Zhang, Lan Zhang, Jing Chen, Qinghai Zeng. Identification of Sitogluside as a Potential Skin-Pigmentation-Reducing Agent through Network Pharmacology. Oxidative medicine and cellular longevity. 2021; 2021(?):4883398. doi: 10.1155/2021/4883398. [PMID: 34603597]
  • Trang T T Nguyen, Ha V H Nguyen. Effects of Fermentation Conditions Using Lactobacillus plantarum on the Charantin, Stigmasterol Glucoside and β-sitosterol Glucoside Contents of Bitter Gourd (Momordica charantia L.) Juice. Plant foods for human nutrition (Dordrecht, Netherlands). 2020 Dec; 75(4):656-658. doi: 10.1007/s11130-020-00860-w. [PMID: 33009632]
  • Merline Ymele Nguedia, Alain Brice Tueche, Abel Joël Gbaweng Yaya, Vincent Yadji, Derek Tantoh Ndinteh, Dieudonné Njamen, Stéphane Zingue. Daucosterol from Crateva adansonii DC (Capparaceae) reduces 7,12-dimethylbenz(a)anthracene-induced mammary tumors in Wistar rats. Environmental toxicology. 2020 Oct; 35(10):1125-1136. doi: 10.1002/tox.22948. [PMID: 32449848]
  • Huiyuan Zhang, Yamin Song, Cong Feng. Improvement of cerebral ischemia/reperfusion injury by daucosterol palmitate-induced neuronal apoptosis inhibition via PI3K/Akt/mTOR signaling pathway. Metabolic brain disease. 2020 08; 35(6):1035-1044. doi: 10.1007/s11011-020-00575-6. [PMID: 32363473]
  • Bing Han, Lingmin Jiang, Pu Jiang, Deqi Zhou, Xiaoxin Jia, Xuegang Li, Xiaoli Ye. Daucosterol linolenate from Sweet Potato Suppresses MCF7-Xenograft-Tumor Growth through Regulating PI3K/AKT Pathway. Planta medica. 2020 Jul; 86(11):767-775. doi: 10.1055/a-1176-1884. [PMID: 32512614]
  • Stéphane Zingue, Abel Joël Gbaweng Yaya, Thomas Michel, Derek Tantoh Ndinteh, Jochen Rutz, Florence Auberon, Sebastian Maxeiner, Felix K-H Chun, Alembert Tiabou Tchinda, Dieudonné Njamen, Roman A Blaheta. Bioguided identification of daucosterol, a compound that contributes to the cytotoxicity effects of Crateva adansonii DC (capparaceae) to prostate cancer cells. Journal of ethnopharmacology. 2020 Jan; 247(?):112251. doi: 10.1016/j.jep.2019.112251. [PMID: 31560992]
  • Claudia Luna-Herrera, Irma A Martínez-Dávila, Luis O Soto-Rojas, Yazmin M Flores-Martinez, Manuel A Fernandez-Parrilla, Jose Ayala-Davila, Bertha A León-Chavez, Guadalupe Soto-Rodriguez, Victor M Blanco-Alvarez, Francisco E Lopez-Salas, Maria E Gutierrez-Castillo, Bismark Gatica-Garcia, America Padilla-Viveros, Cecilia Bañuelos, David Reyes-Corona, Armando J Espadas-Alvarez, Linda Garcés-Ramírez, Oriana Hidalgo-Alegria, Fidel De La Cruz-López, Daniel Martinez-Fong. Intranigral Administration of β-Sitosterol-β-D-Glucoside Elicits Neurotoxic A1 Astrocyte Reactivity and Chronic Neuroinflammation in the Rat Substantia Nigra. Journal of immunology research. 2020; 2020(?):5907591. doi: 10.1155/2020/5907591. [PMID: 33282962]
  • Samia Baatouche, Thamere Cheriet, Djamel Sarri, Ratiba Mekkiou, Ouahiba Boumaza, Samir Benayache, Fadila Benayache, Ignacio Brouard, Francisco León, Ramdane Seghiri. Centaurea microcarpa Coss. & Dur. (Asteraceae) extracts: New cyanogenic glucoside and other constituents. Natural product research. 2019 Nov; 33(21):3070-3076. doi: 10.1080/14786419.2018.1517343. [PMID: 30445872]
  • Herminia López-Salazar, Brenda Hildeliza Camacho-Díaz, Sandra Victoria Ávila-Reyes, Ma Dolores Pérez-García, Manases González-Cortazar, Martha L Arenas Ocampo, Antonio R Jiménez-Aparicio. Identification and Quantification of β-Sitosterol β-d-Glucoside of an Ethanolic Extract Obtained by Microwave-Assisted Extraction from Agave angustifolia Haw. Molecules (Basel, Switzerland). 2019 Oct; 24(21):. doi: 10.3390/molecules24213926. [PMID: 31683500]
  • Navneet Kishore, Pradeep Kumar, Karuna Shanker, Akhilesh Kumar Verma. Human disorders associated with inflammation and the evolving role of natural products to overcome. European journal of medicinal chemistry. 2019 Oct; 179(?):272-309. doi: 10.1016/j.ejmech.2019.06.034. [PMID: 31255927]
  • Tamilselvam Rajavel, Gunasekeran Banu Priya, Venkatesan Suryanarayanan, Sanjeev Kumar Singh, Kasi Pandima Devi. Daucosterol disturbs redox homeostasis and elicits oxidative-stress mediated apoptosis in A549 cells via targeting thioredoxin reductase by a p53 dependent mechanism. European journal of pharmacology. 2019 Jul; 855(?):112-123. doi: 10.1016/j.ejphar.2019.04.051. [PMID: 31059712]
  • Ali M El-Halawany, Samir M Osman, Hossam M Abdallah. Cytotoxic constituents from Vicia monantha subsp. monantha seeds. Natural product research. 2019 Jun; 33(12):1783-1786. doi: 10.1080/14786419.2018.1434638. [PMID: 29411647]
  • Jian-Hua Shao, Jia Chen, Xiao-Qing Xu, Chun-Chao Zhao, Zi-Ling Dong, Wen-Yan Liu, Jie Shen. Chemical constituents and biological activities of Viburnum macrocephalum f. keteleeri. Natural product research. 2019 Jun; 33(11):1612-1616. doi: 10.1080/14786419.2018.1428593. [PMID: 29368956]
  • Ping Gao, Xiaopeng Huang, Tingting Liao, Guangsen Li, Xujun Yu, Yaodong You, Yuxing Huang. Daucosterol induces autophagic-dependent apoptosis in prostate cancer via JNK activation. Bioscience trends. 2019 May; 13(2):160-167. doi: 10.5582/bst.2018.01293. [PMID: 30944266]
  • Abdelaaty A Shahat, Syed Hidayathulla, Azmat A Khan, Amer M Alanazi, Osaid T Al Meanazel, Ali S Alqahtani, Mansour S Alsaid, Ahmed A Hussein. Phytochemical profiling, antioxidant and anticancer activities of Gastrocotyle hispida growing in Saudi Arabia. Acta tropica. 2019 Mar; 191(?):243-247. doi: 10.1016/j.actatropica.2019.01.013. [PMID: 30659804]
  • Nuan Ma, Qin Tang, Wan-Ting Wu, Xin-An Huang, Qin Xu, Guang-Li Rong, Song Chen, Jian-Ping Song. Three Constituents of Moringa oleifera Seeds Regulate Expression of Th17-Relevant Cytokines and Ameliorate TPA-Induced Psoriasis-Like Skin Lesions in Mice. Molecules (Basel, Switzerland). 2018 Dec; 23(12):. doi: 10.3390/molecules23123256. [PMID: 30544700]
  • Bing Han, Pu Jiang, Wuyang Liu, Heshan Xu, Yuanfeng Li, Zhaoxing Li, Hang Ma, Yang Yu, Xuegang Li, Xiaoli Ye. Role of Daucosterol Linoleate on Breast Cancer: Studies on Apoptosis and Metastasis. Journal of agricultural and food chemistry. 2018 Jun; 66(24):6031-6041. doi: 10.1021/acs.jafc.8b01387. [PMID: 29878766]
  • Dinara Satmbekova, Radhakrishnan Srivedavyasasri, Yerkebulan Orazbekov, Roza Omarova, Ubaidilla Datkhayev, Samir A Ross. Chemical and biological studies on Cichorium intybus L. Natural product research. 2018 Jun; 32(11):1343-1347. doi: 10.1080/14786419.2017.1343319. [PMID: 28629227]
  • Lashyn Kiyekbayeva, Nesma M Mohamed, Orazbekov Yerkebulan, Enas I Mohamed, Datkhayev Ubaidilla, Akhtayeva Nursulu, Mamurova Assem, Radhakrishnan Srivedavyasasri, Samir A Ross. Phytochemical constituents and antioxidant activity of Echinops albicaulis. Natural product research. 2018 May; 32(10):1203-1207. doi: 10.1080/14786419.2017.1323213. [PMID: 28475371]
  • Radhakrishnan Srivedavyasasri, Miriah B White, Tatyana S Kustova, Nadezhda G Gemejiyeva, Charles L Cantrell, Samir A Ross. New tetranorlabdanoic acid from aerial parts of Salvia aethiopis. Natural product research. 2018 Jan; 32(1):14-17. doi: 10.1080/14786419.2017.1324961. [PMID: 28475363]
  • Shikha Mishra, Vidhu Aeri. Biotransformation of lignan glycoside to its aglycone by Woodfordia fruticosa flowers: quantification of compounds using a validated HPTLC method. Pharmaceutical biology. 2017 Dec; 55(1):360-366. doi: 10.1080/13880209.2016.1238948. [PMID: 27931157]
  • Jerald J Nair, Anke Wilhelm, Susanna L Bonnet, Johannes van Staden. Antibacterial constituents of the plant family Amaryllidaceae. Bioorganic & medicinal chemistry letters. 2017 11; 27(22):4943-4951. doi: 10.1016/j.bmcl.2017.09.052. [PMID: 29033234]
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