Stevioside (BioDeep_00000000005)
human metabolite PANOMIX_OTCML-2023 Endogenous
代谢物信息卡片
化学式: C38H60O18 (804.3779460000001)
中文名称: 甜菊苷, 甜菊糖
谱图信息:
最多检出来源 Viridiplantae(plant) 0.5%
Last reviewed on 2024-08-26.
Cite this Page
Stevioside. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/stevioside (retrieved
2024-09-08) (BioDeep RN: BioDeep_00000000005). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: C=C1CC23CCC4C(C)(C(=O)OC5OC(CO)C(O)C(O)C5O)CCCC4(C)C2CCC1(OC1OC(CO)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O)C3
InChI: InChI=1S/C38H60O18/c1-16-11-37-9-5-20-35(2,7-4-8-36(20,3)34(50)55-32-29(49)26(46)23(43)18(13-40)52-32)21(37)6-10-38(16,15-37)56-33-30(27(47)24(44)19(14-41)53-33)54-31-28(48)25(45)22(42)17(12-39)51-31/h17-33,39-49H,1,4-15H2,2-3H3/t17-,18-,19-,20+,21+,22-,23-,24-,25+,26+,27+,28-,29-,30-,31+,32+,33+,35-,36-,37-,38+/m1/s1
描述信息
Stevioside is a diterpene glycoside that is rubusoside in which the hydroxy group at position 2 of the allylic beta-D-glucoside has been converted to the corresponding beta-D-glucoside. It is a natural herbal sweetener that is 250-300 times sweeter than sucrose (though with a bitter aftertaste), extracted from the Stevia rebaudiana plant native to South America. It has a role as a sweetening agent, an antioxidant, an antineoplastic agent, a hypoglycemic agent, an anti-inflammatory agent and a plant metabolite. It is a diterpene glycoside, an ent-kaurane diterpenoid, a beta-D-glucoside, a tetracyclic diterpenoid and a bridged compound. It is functionally related to a steviol and a rubusoside.
Stevioside is a natural product found in Asteraceae, Stevia rebaudiana, and Bos taurus with data available.
See also: Stevia rebaudiuna Leaf (part of).
Stevioside is a constituent of Stevia rebaudiana (stevia). Sweetening agent which is 300 times sweeter than sucrose. Stevia rebaudiana is extensively cultivated in Japan, and Stevioside is a permitted sweetener in that country Rebaudioside B, D, and E may also be present in minute quantities; however, it is suspected that rebaudioside B is a byproduct of the isolation technique. The two majority compounds stevioside and rebaudioside, primarily responsible for the sweet taste of stevia leaves, were first isolated by two French chemists in 1931
A diterpene glycoside that is rubusoside in which the hydroxy group at position 2 of the allylic beta-D-glucoside has been converted to the corresponding beta-D-glucoside. It is a natural herbal sweetener that is 250-300 times sweeter than sucrose (though with a bitter aftertaste), extracted from the Stevia rebaudiana plant native to South America.
Constituent of Stevia rebaudiana (stevia). Sweetening agent which is 300 times sweeter than sucrose. Stevia rebaudiana is extensively cultivated in Japan, and Stevioside is a permitted sweetener in that country
D000074385 - Food Ingredients > D005503 - Food Additives
D010592 - Pharmaceutic Aids > D005421 - Flavoring Agents
Stevioside is a natural sweetener extracted from leaves of Stevia rebaudiana, with anticancer activity[1].
Stevioside is a natural sweetener extracted from leaves of Stevia rebaudiana, with anticancer activity[1].
Stevioside. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=57817-89-7 (retrieved 2024-08-26) (CAS RN: 57817-89-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
同义名列表
45 个代谢物同义名
(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (1R,4S,5R,9S,10R,13S)-13-{[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecane-5-carboxylate; [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl] [(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-tetrahydropyran-2-yl]oxy-dimethyl-methylene-[?]carboxylate; 1-O-{(5beta,8alpha,9beta,10alpha,13alpha)-13-[(2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy]-18-oxokaur-16-en-18-yl}-beta-D-glucopyranose; 1-O-{13alpha-[(2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy]-18-oxo-5beta,8alpha,9beta,10alpha-kaur-16-en-18-yl}-beta-D-glucopyranose; 1-O-(13alpha-((2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy)-18-oxo-5beta,8alpha,9beta,10alpha-kaur-16-en-18-yl)-beta-D-glucopyranose; KAUR-16-EN-18-OIC ACID, 13-((2-O-.BETA.-D-GLUCOPYRANOSYL-.BETA.-D-GLUCOPYRANOSYL)OXY)-, .BETA.-D-GLUCOPYRANOSYL ESTER, (4.ALPHA.)-; (4.ALPHA.)-13-((2-O-.BETA.-D-GLUCOPYRANOSYL-.BETA.-D-GLUCOPYRANOSYL)OXY)KAUR-16-EN-18-OIC ACID .BETA.-D-GLUCOPYRANOSYL ESTER; KAUR-16-EN-18-OIC ACID, 13-((2-O-beta-D-GLUCOPYRANOSYL-beta-D-GLUCOPYRANOSYL)OXY)-, beta-D-GLUCOPYRANOSYL ESTER, (4alpha)-; 13-[(2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy]-kaur-16-en-18-oic acid, (4alpha)-beta-D-glucopyranosyl ester; (4alpha)-13-((2-O-beta-D-GLUCOPYRANOSYL-beta-D-GLUCOPYRANOSYL)OXY)KAUR-16-EN-18-OIC ACID beta-D-GLUCOPYRANOSYL ESTER; 13-[(2-O-.beta.-D-Glucopyranosyl-.alpha.-D-glucopyranosyl)oxy]kaur-16-en-18-oic acid .beta.-D-glucopyranosyl ester; 13-((2-O-.beta.-D-Glucopyranosyl-.alpha.-D-glucopyranosyl)oxy)kaur-16-en-18-oic acid .beta.-D-glucopyranosyl ester; Kaur-16-en-18-oic acid, 13-((2-O-beta-D-glucopyranosyl-alpha-D-glucopyranosyl)oxy)-, beta-D-glucopyranosyl ester; 13-((2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy)kaur-16-en-18-oic acid beta-D-glucopyranosyl ester; 13-[(2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy]kaur-16-en-18-oic acid beta-D-glucopyranosyl ester; Kaur-16-en-18-oic acid,13-[(2-O-b-D-glucopyranosyl-b-D-glucopyranosyl)oxy]-,b-D-glucopyranosyl ester, (4a)-; (4alpha)-beta-D-Glucopyranosyl 13-((2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy)kaur-16-en-18-oate; 13-[(2-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy]kaur-16-en-18-Oate beta-D-glucopyranosyl ester; 13-[(2-O-Β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]kaur-16-en-18-Oic acid β-D-glucopyranosyl ester; 13-[(2-O-b-D-Glucopyranosyl-b-D-glucopyranosyl)oxy]kaur-16-en-18-Oic acid b-D-glucopyranosyl ester; 13-[(2-O-Β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]kaur-16-en-18-Oate β-D-glucopyranosyl ester; 13-[(2-O-b-D-Glucopyranosyl-b-D-glucopyranosyl)oxy]kaur-16-en-18-Oate b-D-glucopyranosyl ester; 4-17-00-03618 (Beilstein Handbook Reference); UEDUENGHJMELGK-HYDKPPNVSA-N; STEVIOSIDE (USP-RS); Diterpene glycoside; STEVIOSIDE [USP-RS]; STEVIOSIDE (MART.); STEVIOSIDE [MART.]; steviol glycoside; STEVIOSIDE [INCI]; UNII-0YON5MXJ9P; STEVIOSIDE [MI]; .ALPHA.-G-SWEET; (-)-STEVIOSIDE; 1,2-Stevioside; alpha-G-SWEET; STEVIBIOSIDE; 0YON5MXJ9P; STEVIAN 50; Stevioside; Eupatorin?; Steviosin; Rebaudin; Stevin?
数据库引用编号
22 个数据库交叉引用编号
- ChEBI: CHEBI:9271
- KEGG: C09189
- PubChem: 442089
- PubChem: 548198
- HMDB: HMDB0034945
- Metlin: METLIN67500
- DrugBank: DB16882
- ChEMBL: CHEMBL444122
- Wikipedia: Stevioside
- LipidMAPS: LMPR01040119
- MeSH: stevioside
- ChemIDplus: 0057817897
- MetaCyc: CPD-14504
- KNApSAcK: C00003485
- foodb: FDB013538
- chemspider: 390625
- CAS: 57817-89-7
- medchemexpress: HY-N0669
- PMhub: MS000002828
- MetaboLights: MTBLC9271
- 3DMET: B02755
- NIKKAJI: J27.441K
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
代谢反应
63 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(63)
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + stevioside ⟶ H+ + UDP + rebaudioside A
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + stevioside ⟶ H+ + UDP + rebaudioside A
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
19-O-β-glucopyranosyl-steviol + UDP-α-D-glucose ⟶ H+ + UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviol ⟶ H+ + UDP + steviolmonoside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + rubusoside ⟶ H+ + UDP + stevioside
- steviol glucoside biosynthesis (rebaudioside A biosynthesis):
UDP-α-D-glucose + steviolmonoside ⟶ UDP + rubusoside
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
53 个相关的物种来源信息
- 33090 甜叶菊: -
- 55670 Stevia rebaudiana:
- 4210 Asteraceae: 10.1002/JSFA.6287
- 55670 Stevia rebaudiana:
- 55670 Stevia rebaudiana:
- 4210 Asteraceae: 10.1002/JSFA.6287
- 55670 Stevia rebaudiana:
- 9606 Homo sapiens: -
- 205692 Forsythia koreana: 10.1016/S0031-9422(00)83456-1
- 205692 Forsythia koreana: 10.1016/S0031-9422(97)01134-5
- 205691 Forsythia viridissima: 10.1016/S0031-9422(00)83456-1
- 205691 Forsythia viridissima: 10.1016/S0031-9422(97)01134-5
- 126358 Abeliophyllum distichum: 10.1016/S0031-9422(97)01134-5
- 363423 Centaurea deflexa: 10.1016/J.EJMECH.2011.03.011
- 2753873 Daphne feddei: 10.1021/NP8004166
- 137893 Saussurea medusa: 10.1248/CPB.53.1416
- 137893 Saussurea medusa: 10.1016/S0304-3835(00)00499-7
- 137893 Saussurea medusa: 10.1016/S0031-9422(01)00429-0
- 205694 Forsythia ovata: 10.1248/CPB.36.3667
- 1486496 Centaurea arenaria: 10.1002/PTR.3187
- 2893703 Saussurea macrota: 10.1002/CHIN.200516160
- 196747 Onopordum acaulon: 10.1016/0031-9422(92)83742-H
- 297478 Onopordum illyricum: 10.1021/NP990098Z
- 254913 Saussurea laniceps: 10.1016/S1875-5364(11)60016-2
- 254913 Saussurea laniceps: 10.1002/HLCA.200790096
- 276781 Trachelospermum asiaticum: 10.1016/0031-9422(72)80115-8
- 276781 Trachelospermum asiaticum: 10.1248/CPB.34.4340
- 373155 Gaillardia aestivalis: 10.1016/S0031-9422(00)95216-6
- 75648 Centaurea imperialis: 10.1016/0031-9422(81)85287-9
- 200489 Saussurea involucrata: 10.1080/10286020.2010.499856
- 4217 Arctium lappa: 10.1248/CPB.44.2300
- 4217 Arctium lappa: 10.1248/BPB.19.1515
- 4217 Arctium lappa: 10.1016/S0031-9422(00)89550-3
- 4217 Arctium lappa: 10.1007/978-1-4613-1855-2_22
- 4217 Arctium lappa: 10.1016/J.PHYMED.2009.04.005
- 4217 Arctium lappa: 10.1007/978-3-540-71095-0_1382
- 4217 Arctium lappa: 10.1016/J.JPBA.2009.03.018
- 429296 Trachelospermum axillare: 10.1016/0031-9422(93)85183-R
- 126418 Forsythia suspensa: 10.1002/RCM.2875
- 947960 Trachelospermum gracilipes: 10.1016/0031-9422(72)80115-8
- 50189 Torreya nucifera: 10.1055/S-2001-15804
- 41536 Centaurea melitensis: 10.1016/J.PHYTOCHEM.2006.08.012
- 41536 Centaurea melitensis: 10.1016/S0305-1978(01)00062-X
- 41506 Plectocephalus americanus: 10.1016/J.PHYTOCHEM.2006.08.012
- 41506 Plectocephalus americanus: 10.1016/S0305-1978(01)00062-X
- 446849 Saussurea salicifolia: 10.1016/J.FCT.2010.05.056
- 75633 Centaurea nigra: 10.1016/S0305-1978(02)00227-2
- 363450 Centaurea sclerolepis: 10.1177/1934578X0600100403
- 145513 Centaurea raphanina: 10.1590/S0102-695X2007000200003
- 69389 Trachelospermum jasminoides: 10.1248/YAKUSHI1947.93.4_539
- 276781 Trachelospermum asiaticum: 10.1248/YAKUSHI1947.93.4_539
- 35608 Artemisia Annua L.: -
- 33090 Plants: -
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
- Joanna Śniegowska, Anita Biesiada, Alan Gasiński. Influence of the Nitrogen Fertilization on the Yield, Biometric Characteristics and Chemical Composition of Stevia rebaudiana Bertoni Grown in Poland.
Molecules (Basel, Switzerland).
2024 Apr; 29(8):. doi:
10.3390/molecules29081865
. [PMID: 38675686] - Shan Li, Shuangshuang Luo, Xingying Zhao, Song Gao, Xiaoyu Shan, Jian Lu, Jingwen Zhou. Efficient Conversion of Stevioside to Rebaudioside M in Saccharomyces cerevisiae by a Engineering Hydrolase System and Prolonging the Growth Cycle.
Journal of agricultural and food chemistry.
2024 Apr; 72(14):8140-8148. doi:
10.1021/acs.jafc.4c01483
. [PMID: 38563232] - Mei-Li Xu, Yuanxin Cheng, Mo Feng, Qingguo Lu, Yunhe Lian. Identifying Potential Sources of Phthalate Contamination in the Leaves of Stevia Rebaudiana (Bertoni) and the Development of Removal Technology.
Molecules (Basel, Switzerland).
2024 Apr; 29(7):. doi:
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International journal of molecular sciences.
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Plant physiology and biochemistry : PPB.
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Plant physiology and biochemistry : PPB.
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Environmental science and pollution research international.
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Preparative biochemistry & biotechnology.
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IUBMB life.
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Cells.
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Molecules (Basel, Switzerland).
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Journal of the science of food and agriculture.
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Journal of pharmaceutical and biomedical analysis.
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Obesity research & clinical practice.
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Enzyme and microbial technology.
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Drug and chemical toxicology.
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Molecules (Basel, Switzerland).
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Molecules (Basel, Switzerland).
2021 Dec; 26(24):. doi:
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Journal of the science of food and agriculture.
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Molecules (Basel, Switzerland).
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Plant cell reports.
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Molecules (Basel, Switzerland).
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Molecular biology reports.
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Drug development research.
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BioMed research international.
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Nutrients.
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Journal of food biochemistry.
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Inflammopharmacology.
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Ultrasonics sonochemistry.
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Food chemistry.
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Molecules (Basel, Switzerland).
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Journal of agricultural and food chemistry.
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Molecular biology reports.
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Scientific reports.
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Analytical and bioanalytical chemistry.
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Journal of the science of food and agriculture.
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Food chemistry.
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Applied microbiology and biotechnology.
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Molecules (Basel, Switzerland).
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Molecules (Basel, Switzerland).
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Food chemistry.
2020 Mar; 308(?):125569. doi:
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Journal of agricultural and food chemistry.
2020 Feb; 68(6):1579-1587. doi:
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Journal of theoretical biology.
2020 02; 486(?):110094. doi:
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Toxicology in vitro : an international journal published in association with BIBRA.
2020 Feb; 62(?):104694. doi:
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PloS one.
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World journal of microbiology & biotechnology.
2019 Dec; 36(1):8. doi:
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Food & function.
2019 Dec; 10(12):7967-7972. doi:
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BMC plant biology.
2019 Oct; 19(1):436. doi:
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Food chemistry.
2019 Oct; 295(?):563-568. doi:
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Plant physiology and biochemistry : PPB.
2019 Oct; 143(?):154-164. doi:
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Clinical nutrition ESPEN.
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Functional plant biology : FPB.
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Nature communications.
2019 07; 10(1):3214. doi:
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BMC plant biology.
2019 Jun; 19(1):274. doi:
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Basic & clinical pharmacology & toxicology.
2019 Jun; 124(6):670-680. doi:
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Plant biotechnology journal.
2019 06; 17(6):1037-1047. doi:
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Food & function.
2019 May; 10(5):2340-2346. doi:
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Life sciences.
2019 May; 224(?):187-196. doi:
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Plant physiology and biochemistry : PPB.
2019 Apr; 137(?):154-161. doi:
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Journal of the science of food and agriculture.
2019 Mar; 99(5):2384-2392. doi:
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Molecules (Basel, Switzerland).
2019 Mar; 24(7):. doi:
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Molecular biology reports.
2019 Feb; 46(1):7-16. doi:
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Food chemistry.
2019 Jan; 272(?):653-662. doi:
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BMC plant biology.
2019 Jan; 19(1):1. doi:
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International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group.
2019; 36(1):302-312. doi:
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