Crustecdysone (BioDeep_00000002779)

Secondary id: BioDeep_00000171790, BioDeep_00000407045, BioDeep_00000410545

human metabolite PANOMIX_OTCML-2023 Endogenous Marine Natural Products Volatile Flavor Compounds

代谢物信息卡片

(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-((2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl)-1,2,3,4,5,9,10,11,12,13,14,15,16,17-tetradecahydro-6H-cyclopenta[a]phenanthren-6-one

化学式: C27H44O7 (480.3086874)
中文名称: β-蜕皮激素, 蜕皮激素, β-蜕皮甾酮
谱图信息: 最多检出来源 Homo sapiens(feces) 0.02%

分子结构信息

SMILES: C1[C@H](O)[C@H](O)C[C@@]2([H])C(=O)C=C3[C@@](CC[C@]4([C@@]3(O)CC[C@]4([H])[C@](O)(C)[C@H](O)CCC(O)(C)C)C)([H])[C@]21C
InChI: InChI=1S/C27H44O7/c1-23(2,32)9-8-22(31)26(5,33)21-7-11-27(34)16-12-18(28)17-13-19(29)20(30)14-24(17,3)15(16)6-10-25(21,27)4/h12,15,17,19-22,29-34H,6-11,13-14H2,1-5H3/t15-,17-,19+,20-,21-,22+,24+,25+,26+,27+/m0/s1

描述信息

20-hydroxyecdysone is an ecdysteroid that is ecdysone substituted by a hydroxy group at position 20. It has a role as a plant metabolite and an animal metabolite. It is a 20-hydroxy steroid, an ecdysteroid, a 14alpha-hydroxy steroid, a 3beta-sterol, a 2beta-hydroxy steroid, a 22-hydroxy steroid, a 25-hydroxy steroid and a phytoecdysteroid. It is functionally related to an ecdysone.
20-Hydroxyecdysone is a natural product found in Asparagus filicinus, Trichobilharzia ocellata, and other organisms with data available.
A steroid hormone that regulates the processes of MOLTING or ecdysis in insects. Ecdysterone is the 20-hydroxylated ECDYSONE.
Crustecdysone is found in crustaceans. Crustecdysone is isolated from the marine crayfish Jasus lalandei in low yield (2 mg/ton
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
An ecdysteroid that is ecdysone substituted by a hydroxy group at position 20.
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Crustecdysone (20-Hydroxyecdysone) is a naturally occurring ecdysteroid hormone isolated from Serratula coronata which controls the ecdysis (moulting) and metamorphosis of arthropods, it inhibits caspase activity and induces autophagy via the 20E nuclear receptor complex, EcR-USP[1]. Crustecdysone exhibits regulatory or protective roles in the cardiovascular system[2]. Crustecdysone is an active metabolite of Ecdysone (HY-N0179)[3].
Crustecdysone (20-Hydroxyecdysone) is a naturally occurring ecdysteroid hormone isolated from Serratula coronata which controls the ecdysis (moulting) and metamorphosis of arthropods, it inhibits caspase activity and induces autophagy via the 20E nuclear receptor complex, EcR-USP[1]. Crustecdysone exhibits regulatory or protective roles in the cardiovascular system[2]. Crustecdysone is an active metabolite of Ecdysone (HY-N0179)[3].

同义名列表

74 个代谢物同义名

(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-((2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl)-1,2,3,4,5,9,10,11,12,13,14,15,16,17-tetradecahydro-6H-cyclopenta[a]phenanthren-6-one; (2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one; (2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(1R,2R)-1,2,5-trihydroxy-1,5-dimethyl-hexyl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one; (1R,2R,4S,5R,7R,11S,14S,15R)-4,5,11-trihydroxy-2,15-dimethyl-14-[(2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-8-one; 2,3,14-Trihydroxy-10,13-dimethyl-17-(1,2,5-trihydroxy-1,5-dimethyl-hexyl)-1,2,3,4,5,9,10,11,12,13,14,15,16,17-tetradecahydro-cyclopenta[a]phenanthren-6-one; Cholest-7-en-6-one, 2,3,14,20,22,25-hexahydroxy-, (2.beta.,3.beta.,5.beta.,22R)-; Cholest-7-en-6-one, 2,3,14,20,22,25-hexahydroxy-, (2-beta,3-beta,5-beta,22R)-; Cholest-7-en-6-one, 2,3,14,20,22,25-hexahydroxy-, (2beta,3beta,5beta,22R)-; 5-beta-Cholest-7-en-6-one, 2-beta,3-beta,14,20,22,25-hexahydroxy-, (22R)-; (2alpha,3alpha,5alpha,22R)-2,3,14,20,22,25-hexahydroxycholest-7-en-6-one; (22R)-2beta,3beta,14alpha,20,22,25-hexahydroxy-5beta-cholest-7-en-6-one; (2beta,3beta,5beta,22R)-2,3,14,20,22,25-hexahydroxycholest-7-en-6-one; 2beta,3beta,14alpha,20R,22R,25-hexahydroxy-5beta-cholest-7-en-6-one; 2beta,3beta,14alpha,20beta,22alpha,25-Hexahydroxycholest-7-en-6-one; 2beta,3beta,14alpha,20,22R,25-hexahydroxy-5beta-cholest-7-en-6-one; Cholest-7-en-6-one, 2,3,14,20,22,25-hexahydroxy-, (2b,3b,5b,22R)-; (2Beta,3beta,5beta)-2,3,14,20,22,25-hexahydroxycholest-7-en-6-one; 2-beta,3-beta,14,20,22,25-Hexahydroxy-5-beta-cholet-7-en-6- one; 2-beta,3-beta,14,20,22,25-Hexahydroxy-5-beta-cholet-7-en-6-one; (2b,3b,5b,22R)-2,3,14,20,22,25-Hexahydroxycholest-7-en-6-one; (2β,3β,5β,22R)-2,3,14,20,22,25-Hexahydroxycholest-7-en-6-one; 2β,3β,14α,20β,22α,25-Hexahydroxycholest-7-en-6-one; 20-Hydroxyecdysone, >=93\\% (HPLC), powder; 20-HYDROXY-.ALPHA.-ECDYSONE; 20-HYDROXYECDYSONE [WHO-DD]; NKDFYOWSKOHCCO-YPVLXUMRSA-N; 20-Hydroxy-alpha-ecdysone; 20-HYDROXYECDYSONE [MI]; B-ecdysone,Commisterone; (+)-20-Hydroxyecdysone; 20-Hydroxy-a-ecdysone; 20-Hydroxy-α-ecdysone; 20R-Hydroxyecdysone; 20 Hydroxyecdysone; 20-Hydroxyecdysone; 20-Hydroxyecdyson; .beta-Ecdysterone; beta-ECDYSTERONE; Isoinokosterone; Hydroxyecdysone; (+)-Ecdysterone; beta-Ecydisone; 20-OH ecdysone; beta-Ecdysone; b-Ecdysterone; Crustecdysone; beta-Ecdisone; Beta Ecdysone; Viticosterone; β-Ecdysterone; Crustecdyson; Commisterone; Polypodine A; Polypodine C; Polypodin C; Ecdysterone; Polypodin A; β-Ecydisone; ?- Ecdysone; ST 27:2;O7; b-Ecdysone; Edysterone; Ecdysteron; Β-ecdysone; AI3-44727; Ecdystene; Sarconeos; Ecdysten; Ekdisten; THE-7; 20-E; 20E; (2S,3R,5R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one; 20-Hydroxyecdysone

数据库引用编号

25 个数据库交叉引用编号

ChEBI: CHEBI:16587
KEGG: C02633
PubChem: 5459840
PubChem: 271605
PubChem: 439770
HMDB: HMDB0030180
DrugBank: DB16935
ChEMBL: CHEMBL224128
Wikipedia: 20-Hydroxyecdysone
LipidMAPS: LMST01010209
MeSH: Ecdysterone
ChemIDplus: 0005289747
MetaCyc: CPD-276
KNApSAcK: C00003654
KNApSAcK: C00048286
chemspider: 4573597
CAS: 5289-74-7
medchemexpress: HY-N6979
PMhub: MS000004946
MetaboLights: MTBLC16587
PubChem: 5613
PDB-CCD: 20E
3DMET: B04858
NIKKAJI: J13.425B
KNApSAcK: 16587

分类词条

代谢反应

1 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(1)

Molting Hormone Biosynthesis: Cholesterol + Hydrogen Ion + NADH + Oxygen ⟶ 7-Dehydrocholesterol + NAD + Water

PharmGKB(0)

170 个相关的物种来源信息

240005 - Achyranthes aspera: 10.1007/PL00010306
384659 - Achyranthes bidentata: 10.1016/0040-4020(76)80160-3
384659 - Achyranthes bidentata Bl.: -
165205 - Afrocarpus gracilior: 10.1016/J.PHYTOL.2012.02.005
295252 - Agelas dispar:
295252 - Agelas dispar: 10.1021/NP970323H
1736745 - Ajuga chamaecistus: 10.1016/S0021-9673(01)88168-1
49984 - Ajuga chamaepitys: 10.1016/S0031-9422(00)84101-1
167911 - Ajuga decumbens: 10.1248/CPB.17.340
2026104 - Ajuga iva: 10.1016/S0031-9422(00)97527-7
984302 - Ajuga nipponensis: 10.1248/CPB.17.340
38596 - Ajuga reptans:
41472 - Amberboa moschata: 10.1016/S0305-1978(97)00018-5
470566 - Anemone alpina: 10.1016/S0305-1978(97)00042-2
387932 - Anemone montana: 10.1016/S0305-1978(97)00042-2
174168 - Anemone occidentalis: 10.1016/S0305-1978(97)00042-2
445234 - Anemone pulsatilla: 10.1016/S0305-1978(97)00042-2
7461 - Apis cerana: 10.1371/JOURNAL.PONE.0175573
72517 - Arilus cristatus: 10.1007/BF01946477
6252 - Ascaris lumbricoides: 10.1007/BF01923635
100515 - Asparagus filicinus: 10.1016/S0031-9422(99)00051-5
65704 - Athyrium yokoscense: 10.1016/0031-9422(95)00688-5
3553 - Atriplex nummularia: 10.1016/S0367-326X(99)00159-8
376799 - Atriplex portulacoides: 10.1016/J.BMCL.2015.03.028
464020 - Axyris amaranthoides: 10.1016/S0031-9422(98)00446-4
6526 - Biomphalaria glabrata: 10.1007/BF01959769
49702 - Blandfordia punicea: 10.1021/NP960377B
122298 - Blitum bonus-henricus: 10.1016/0031-9422(82)80057-5
7091 - Bombyx mori:
120713 - Brainea insignis: 10.1016/J.PHYTOCHEM.2010.03.002
41536 - Centaurea melitensis:
80839 - Charybdis japonica: 10.1073/PNAS.86.17.6826
46091 - Chenopodiastrum murale: 10.1002/(SICI)1520-6327(1999)41:1<18::AID-ARCH4>3.0.CO;2-T
3559 - Chenopodium album:
882375 - Chenopodium pallidicaule: 10.1016/0305-1978(96)00019-1
63459 - Chenopodium quinoa:
63459 - Chenopodium quinoa: 10.1021/JF0014462
79782 - Cimex lectularius: 10.1007/BF01946477
87754 - Cistanche phelypaea: 10.1248/CPB.38.1927
161397 - Cistanche tubulosa: 10.1248/CPB.38.1927
6535 - Cornu aspersum: 10.1007/BF01959769
1503182 - Cyanotis arachnoidea: 10.1080/10286020290019631
384660 - Cyathula officinalis Kuan: -
84614 - Cyrtomium falcatum: 10.1248/CPB.17.340
4164 - Digitalis purpurea: 10.1007/S10600-010-9551-3
152356 - Diploclisia: 10.1055/S-2007-969388
152357 - Diploclisia glaucescens:
191328 - Dysdercus cingulatus: 10.1007/BF01946477
527504 - Fibraurea chloroleuca: 10.1002/PTR.2650070406
461588 - Fibraurea tinctoria: 10.1002/PTR.2650070406
46114 - Froelichia floridana:
59080 - Gagea serotina: 10.1016/S0305-1978(01)00021-7
2528985 - Gomphrena affinis: 10.1016/S0305-1978(97)00106-3
2528987 - Gomphrena canescens: 10.1016/S0305-1978(97)00106-3
2528988 - Gomphrena cunninghamii: 10.1016/S0305-1978(97)00106-3
221775 - Gomphrena globosa: 10.1016/S0305-1978(97)00106-3
240061 - Gomphrena haageana: 10.1016/S0305-1978(97)00106-3
221778 - Gomphrena serrata: 10.1016/S0305-1978(97)00106-3
2873767 - Haematocarpus subpeltatus: 10.1002/PTR.2650070406
171888 - Helleborus cyclophyllus: 10.1016/J.JEP.2020.112954
171897 - Helleborus odorus:
171898 - Helleborus orientalis: 10.1016/J.PHYTOCHEM.2007.11.007
171899 - Helleborus purpurascens:
171901 - Helleborus torquatus: 10.1016/J.PHYTOCHEM.2007.11.007
171901 - Helleborus torquatus: 10.1016/S0031-9422(01)00070-X
171903 - Helleborus viridis: 10.3109/13880209009082817
9606 - Homo sapiens: -
283497 - Iotrochota birotulata: 10.1016/S0039-128X(99)00096-3
82527 - Ipheion uniflorum: 10.1248/CPB.42.1116
305367 - Klasea centauroides: 10.1007/BF00574363
305371 - Klasea erucifolia:
354313 - Klasea marginata: 10.1007/BF00574363
354317 - Klasea procumbens: 10.1007/BF00574363
305379 - Klasea quinquefolia: 10.1007/BF00574363
354320 - Klasea sogdiana: 10.1007/BF00574363
224738 - Lepidothamnus intermedius: 10.1071/CH9721935
699700 - Lepisorus ussuriensis: 10.1016/S0031-9422(99)00056-4
42439 - Limnanthes alba: 10.1515/ZNC-2001-11-1214
28973 - Limnanthes douglasii: 10.1016/S0031-9422(96)00591-2
13824 - Lygodium japonicum: 10.1007/S11418-009-0376-Y
13123 - Lymantria dispar: 10.1002/ARCH.940010404
6523 - Lymnaea stagnalis: 10.1007/BF01959769
7130 - Manduca sexta:
3498 - Morus alba L.: -
253767 - Neocheiropteris palmatopedata: 10.1007/S10600-010-9560-2
85310 - Nezara viridula: 10.1007/BF01946477
144308 - Nierembergia hippomanica: 10.1016/0031-9422(95)00731-8
274375 - Nierembergia linariifolia: 10.1016/0031-9422(95)00731-8
7536 - Oncopeltus fasciatus: 10.1007/BF01946477
292312 - Ourisia caespitosa: 10.1016/S0305-1978(96)00083-X
292327 - Ourisia macrocarpa: 10.1016/S0305-1978(96)00083-X
292330 - Ourisia macrophylla: 10.1016/S0305-1978(96)00083-X
86596 - Palythoa: 10.1007/BF00598556
44685 - Panax japonicus: 10.1002/HLCA.201100085
44924 - Parazoanthus:
49666 - Paris polyphylla:
49666 - Paris polyphylla: 10.1016/J.FITOTE.2008.09.010
221254 - Paris polyphylla var. chinensis:
231488 - Paris quadrifolia: 10.1007/BF00574363
2708930 - Penianthus zenkeri: 10.1016/0031-9422(91)85047-4
265172 - Penstemon venustus: 10.1016/0031-9422(94)00948-S
221785 - Pfaffia glomerata:
451963 - Pfaffia iresinoides:
41506 - Plectocephalus americanus:
90697 - Plenasium banksiifolium: 10.1055/S-0028-1097493
29025 - Podisus maculiventris: 10.1007/BF01946477
38391 - Polypodium fauriei: 10.1248/CPB.17.340
872808 - Polypodium virginianum:
58048 - Polypodium vulgare:
1729754 - Poranopsis discifera: 10.1016/0039-128X(76)90006-4
32101 - Pteridium aquilinum: 10.1016/S0031-9422(00)89065-2
261975 - Pycnogonum litorale: 10.1515/ZNC-1994-5-615
362630 - Rhaponticum carthamoides:
362636 - Rhaponticum integrifolium:
362639 - Rhaponticum lyratum: 10.1007/BF00574363
362646 - Rhaponticum uniflorum:
362646 - Rhaponticum uniflorum: 10.1016/J.PHYTOCHEM.2009.04.008
13249 - Rhodnius prolixus: 10.1007/BF01946477
254022 - Sagina japonica: 10.1007/S10600-010-9729-8
7010 - Schistocerca gregaria: 10.1039/C39810000418
65004 - Serratula tinctoria:
65004 - Serratula tinctoria: 10.1016/S0031-9422(01)00308-9
108380 - Sida spinosa: 10.1016/S0031-9422(03)00021-9
1930050 - Sida szechuensis: 10.14233/AJCHEM.2014.15427
1137874 - Silene banksia: 10.1007/BF00574584
1137874 - Silene banksia: 10.1007/BF00598381
1937749 - Silene brahuica:
39855 - Silene chalcedonica:
39855 - Silene chalcedonica: 10.1007/BF00636590
411984 - Silene fortunei: 10.1007/BF00574584
1080098 - Silene indica:
42037 - Silene italica: 10.1021/NP0205194
37657 - Silene latifolia: 10.1007/BF00574363
39891 - Silene linicola:
39894 - Silene nemoralis: 10.1007/BF00574584
39894 - Silene nemoralis: 10.1021/NP0205194
42038 - Silene nutans:
42039 - Silene otites:
2039599 - Silene spergulifolia: 10.1007/BF02254804
1309628 - Silene supina: 10.1007/BF02254804
39917 - Silene tatarica:
663359 - Silene turkestanica:
335148 - Silene viridiflora:
2082040 - Silene wallichiana:
1850527 - Silene wilfordii: 10.1007/BF00636589
3562 - Spinacia oleracea:
167472 - Stachyurus himalaicus: 10.3390/12030536
85277 - Stachyurus praecox: 10.1248/CPB.17.340
72122 - Tapinella atrotomentosa:
80604 - Tapinella panuoides: 10.1016/S0031-9422(98)00448-8
46220 - Taxus brevifolia: 10.1016/0031-9422(95)00672-9
99806 - Taxus cuspidata:
285590 - Tinospora cordifolia:
100602 - Trichobilharzia ocellata: 10.1016/0166-6851(91)90139-W
49675 - Trillium camschatcense: 10.1248/CPB.55.551
50545 - Trillium erectum: 10.1016/J.PHYTOCHEM.2008.10.019
82499 - Trillium smallii: 10.1248/CPB.17.340
82502 - Trillium tschonoskii: 10.1248/CPB.17.340
87477 - Trisetum flavescens: 10.1016/S0305-1978(97)00087-2
413480 - Vitex canescens:
2364071 - Vitex cymosa: 10.1016/S0367-326X(00)00304-X
413482 - Vitex glabrata: 10.1021/NP50044A041
1899206 - Vitex madiensis:
1365883 - Vitex megapotamica: 10.1002/ARDP.19723051007
548852 - Vitex pinnata: 10.1016/S0031-9422(00)94985-9
2709034 - Vitex thyrsiflora: 10.1016/S0021-9673(01)90442-X
548845 - Vitex tripinnata: 10.1016/S0031-9422(98)00411-7
86683 - Woodwardia orientalis: 10.1248/CPB.41.1803
105401 - Zoanthus: 10.1021/NP010645S
33090 - 珍珠露水草: -

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

Susana Tavares Cotrim Ribeiro, Naiara Cássia Gancedo, Arildo José Braz de Oliveira, Regina Aparecida Correia Gonçalves. A comprehensive review of Pfaffia glomerata botany, ethnopharmacology, phytochemistry, biological activities, and biotechnology. Journal of ethnopharmacology. 2024 Jun; 328(?):118003. doi: 10.1016/j.jep.2024.118003. [PMID: 38484957]
Hai-Chao Wang, Ling Li, Jing-Hang Zhang, Zhi-Han Yao, Bao-Ping Pang. MicroRNA miR-7-5p targets MARK2 to control metamorphosis in Galeruca daurica. Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology. 2024 Jun; 272(?):110967. doi: 10.1016/j.cbpb.2024.110967. [PMID: 38521445]
Velislava Todorova, Stanislava Ivanova, Dzhevdet Chakarov, Krasimir Kraev, Kalin Ivanov. Ecdysterone and Turkesterone-Compounds with Prominent Potential in Sport and Healthy Nutrition. Nutrients. 2024 May; 16(9):. doi: 10.3390/nu16091382. [PMID: 38732627]
Yu-Xing Zhang, Qiao Tan, Lin Jin, Guo-Qing Li. Molecular characterization of the cytochrome P450 enzyme CYP18A1 in Henosepilachna vigintioctopunctata. Archives of insect biochemistry and physiology. 2024 Apr; 115(4):e22111. doi: 10.1002/arch.22111. [PMID: 38628055]
Haihui Xing, Guohua Chen, Faisal Raza, Hajra Zafar, Lei Xing, Qiaoyun Li, Ran Li, Shanshan Xu, Dan Chen. The Protective Effects of Ecdysterone on Cognitive Impairment through Regulating Akt/GSK-3β/Nrf2 Signaling Pathway and Oxidative Stress in Cognitive Mice Model and Aβ-Induced Cell Neurotoxicity. Frontiers in bioscience (Landmark edition). 2024 Mar; 29(3):109. doi: 10.31083/j.fbl2903109. [PMID: 38538266]
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Jia Wang, Li-Lin Ran, Ying Li, Ying-Hong Liu. Comparative proteomics provides insights into diapause program of Bactrocera minax (Diptera: Tephritidae). PloS one. 2020; 15(12):e0244493. doi: 10.1371/journal.pone.0244493. [PMID: 33382763]
Pengfei Han, Jiao Han, Min Zhang, Jiqiao Fan, Qitian Gong, Enbo Ma, Jianzhen Zhang. 20-Hydroxyecdysone enhances Immulectin-1 mediated immune response against entomogenous fungus in Locusta migratoria. Pest management science. 2020 Jan; 76(1):304-313. doi: 10.1002/ps.5515. [PMID: 31207079]
Jia Zeng, Xianchao Shang, Peng Zhang, Hongwei Wang, Yanlong Gu, Jia-Neng Tan. Combined Use of Deep Eutectic Solvents, Macroporous Resins, and Preparative Liquid Chromatography for the Isolation and Purification of Flavonoids and 20-Hydroxyecdysone from Chenopodium quinoa Willd. Biomolecules. 2019 11; 9(12):. doi: 10.3390/biom9120776. [PMID: 31775374]
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Ayoub Ajaha, Noureddin Bouayad, Ahmed Aarab, Kacem Rharrabe. Effect of 20-Hydroxyecdysone, a Phytoecdysteroid, on Development, Digestive, and Detoxification Enzyme Activities of Tribolium castaneum (Coleoptera: Tenebrionidae). Journal of insect science (Online). 2019 Sep; 19(5):. doi: 10.1093/jisesa/iez097. [PMID: 31639190]
Niramaya S Muchate, Nilima S Rajurkar, Penna Suprasanna, Tukaram D Nikam. NaCl induced salt adaptive changes and enhanced accumulation of 20-hydroxyecdysone in the in vitro shoot cultures of Spinacia oleracea (L.). Scientific reports. 2019 08; 9(1):12522. doi: 10.1038/s41598-019-48737-6. [PMID: 31467324]
Li-Wei Lin, Fan-Hsuan Tsai, Wan-Cheng Lan, Yih-Dih Cheng, Sheng-Chi Lee, Chi-Rei Wu. Steroid-Enriched Fraction of Achyranthes bidentata Protects Amyloid β Peptide 1-40-Induced Cognitive Dysfunction and Neuroinflammation in Rats. Molecular neurobiology. 2019 Aug; 56(8):5671-5688. doi: 10.1007/s12035-018-1436-7. [PMID: 30666561]
Md Abdullah Al Baki, Dae-Weon Lee, Jin Kyo Jung, Yonggyun Kim. Insulin signaling mediates previtellogenic development and enhances juvenile hormone-mediated vitellogenesis in a lepidopteran insect, Maruca vitrata. BMC developmental biology. 2019 07; 19(1):14. doi: 10.1186/s12861-019-0194-8. [PMID: 31277577]
Eduard Isenmann, Gabriella Ambrosio, Jan Felix Joseph, Monica Mazzarino, Xavier de la Torre, Philipp Zimmer, Rymantas Kazlauskas, Catrin Goebel, Francesco Botrè, Patrick Diel, Maria Kristina Parr. Ecdysteroids as non-conventional anabolic agent: performance enhancement by ecdysterone supplementation in humans. Archives of toxicology. 2019 07; 93(7):1807-1816. doi: 10.1007/s00204-019-02490-x. [PMID: 31123801]
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X Liu, S Zhang, Z J Shen, Y Liu, Z Li, X Liu. Vrille is required for larval moulting and metamorphosis of Helicoverpa armigera (Lepidoptera: Noctuidae). Insect molecular biology. 2019 06; 28(3):355-371. doi: 10.1111/imb.12557. [PMID: 30485565]
Xinhai Ye, Le Xu, Xiang Li, Kang He, Hongxia Hua, Zhenghong Cao, Jiadan Xu, Wanyi Ye, Jiao Zhang, Zhuting Yuan, Fei Li. miR-34 modulates wing polyphenism in planthopper. PLoS genetics. 2019 06; 15(6):e1008235. doi: 10.1371/journal.pgen.1008235. [PMID: 31242182]
Dong Wei, Ying-Xin Zhang, Yu-Wei Liu, Wei-Jun Li, Zhi-Xian Chen, Guy Smagghe, Jin-Jun Wang. Gene expression profiling of ovary identified eggshell proteins regulated by 20-hydroxyecdysone in Bactrocera dorsalis. Comparative biochemistry and physiology. Part D, Genomics & proteomics. 2019 06; 30(?):206-216. doi: 10.1016/j.cbd.2019.03.006. [PMID: 30909163]
Diego Silva Batista, Andréa Dias Koehler, Elisson Romanel, Vinícius Cairus de Souza, Tatiane Dulcineia Silva, Maíra Carolina Almeida, Talles Elisson F Maciel, Perácio Rafael Bueno Ferreira, Sérgio Heitor Sousa Felipe, Cleber Witt Saldanha, Joseila Maldaner, Leonardo Lucas Carnevalli Dias, Reginaldo Alves Festucci-Buselli, Wagner Campos Otoni. De novo assembly and transcriptome of Pfaffia glomerata uncovers the role of photoautotrophy and the P450 family genes in 20-hydroxyecdysone production. Protoplasma. 2019 May; 256(3):601-614. doi: 10.1007/s00709-018-1322-1. [PMID: 30357479]
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Renata Vardanega, Aline F V Muzio, Eric Keven Silva, Ana Silvia Prata, M Angela A Meireles. Obtaining functional powder tea from Brazilian ginseng roots: Effects of freeze and spray drying processes on chemical and nutritional quality, morphological and redispersion properties. Food research international (Ottawa, Ont.). 2019 02; 116(?):932-941. doi: 10.1016/j.foodres.2018.09.030. [PMID: 30717026]
J-J Wu, Z-C Chen, Y-W Wang, K-Y Fu, W-C Guo, G-Q Li. Silencing chitin deacetylase 2 impairs larval-pupal and pupal-adult molts in Leptinotarsa decemlineata. Insect molecular biology. 2019 02; 28(1):52-64. doi: 10.1111/imb.12524. [PMID: 30058750]
Hongwei Wang, Jianeng Tan, Xianchao Shang, Xuan Zheng, Xinmin Liu, Jing Wang, Xiaodong Hou, Yongmei Du. Porous organic cage incorporated monoliths for solid-phase extraction coupled with liquid chromatography-mass spectrometry for identification of ecdysteroids from Chenopodium quinoa Willd. Journal of chromatography. A. 2019 Jan; 1583(?):55-62. doi: 10.1016/j.chroma.2018.11.019. [PMID: 30477713]
Qing-Wei Meng, Qing-Yu Xu, Tao-Tao Zhu, Lin Jin, Kai-Yun Fu, Wen-Chao Guo, Guo-Qing Li. Hormonal signaling cascades required for phototaxis switch in wandering Leptinotarsa decemlineata larvae. PLoS genetics. 2019 01; 15(1):e1007423. doi: 10.1371/journal.pgen.1007423. [PMID: 30615614]
Pan Deng, Qing-Yu Xu, Kai-Yun Fu, Wen-Chao Guo, Guo-Qing Li. RNA interference against the putative insulin receptor substrate gene chico affects metamorphosis in Leptinotarsa decemlineata. Insect biochemistry and molecular biology. 2018 12; 103(?):1-11. doi: 10.1016/j.ibmb.2018.10.001. [PMID: 30296480]
N S Muchate, N S Rajurkar, P Suprasanna, T D Nikam. Evaluation of Spinacia oleracea (L.) for phytodesalination and augmented production of bioactive metabolite, 20-hydroxyecdysone. International journal of phytoremediation. 2018 Aug; 20(10):981-994. doi: 10.1080/15226514.2018.1452184. [PMID: 30095306]