Chalconaringenin (BioDeep_00000000100)
Secondary id: BioDeep_00000270019
human metabolite PANOMIX_OTCML-2023 Endogenous PANOMIX-Anthocyanidin
代谢物信息卡片
2-Propen-1-one, 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)-, (2E)-
化学式: C15H12O5 (272.0685)
中文名称: 柚皮素查尔酮, 柚皮素, 柚皮苷查尔酮
谱图信息:
最多检出来源 Homo sapiens(plant) 14.35%
Reviewed
Last reviewed on 2024-07-12.
Cite this Page
Chalconaringenin. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/chalconaringenin (retrieved
2024-12-23) (BioDeep RN: BioDeep_00000000100). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: c1(cc(c(c(c1)O)C(=O)/C=C/c1ccc(cc1)O)O)O
InChI: InChI=1S/C15H12O5/c16-10-4-1-9(2-5-10)3-6-12(18)15-13(19)7-11(17)8-14(15)20/h1-8,16-17,19-20H/b6-3+
描述信息
2,4,4,6-tetrahydroxychalcone is a member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 2 ,4, 4, and 6 respectively. It has a role as a metabolite, an anti-allergic agent and an anti-inflammatory agent. It is a polyphenol and a member of chalcones. It is functionally related to a trans-chalcone.
Naringenin chalcone is a natural product found in Populus koreana, Populus tremula, and other organisms with data available.
Isolated from tomato fruit cuticles. Chalconaringenin is found in many foods, some of which are cherry tomato, lettuce, greenthread tea, and lemon.
A member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 2 ,4, 4, and 6 respectively.
Chalconaringenin is found in garden tomato. Chalconaringenin is isolated from tomato fruit cuticle
Naringenin chalcone. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=5071-40-9 (retrieved 2024-07-12) (CAS RN: 25515-46-2). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
同义名列表
31 个代谢物同义名
2-Propen-1-one, 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)-, (2E)-; (2E)- 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)-2-Propen-1-one; (2E)-3-(4-Hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)-2-propen-1-one; 3-(4-Hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)-2-propen-1-one, 9CI; (2E)-3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one; (E)-3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one; 2-Propen-1-one, 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)-; 3-(4-hydroxyphemyl)-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one; 3-(4-Hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)-2-propen-1-one; trans-2,4,4,6-Tetrahydroxychalcone; Chalcone, 2,4,4,6-tetrahydroxy-; naringenin chalcone, (E)-isomer; trans-2464-tetrahydroxychalcone; 4,2,4,6-TETRAHYDROXYCHALCONE; 4,2,4,6-Tetrahydroxychalcone; 2,4,4,6-tetrahydroxychalcone; 2,4,6,4-tetrahydroxychalcone; YQHMWTPYORBCMF-ZZXKWVIFSA-N; 2464-Tetrahydroxychalcone; (E)-Naringenin chalcone; Naringenin chalcone; Naringenin chalcon; Chalcononaringenin; chalconaringenin; UNII-YCF6Z24AS2; MEGxp0_001759; Isosalipurpol; ACon1_001222; YCF6Z24AS2; Naringenin; Naringenin chalcone
数据库引用编号
34 个数据库交叉引用编号
- ChEBI: CHEBI:15413
- KEGG: C06561
- PubChem: 5280960
- PubChem: 155802
- HMDB: HMDB0029631
- Metlin: METLIN3402
- ChEMBL: CHEMBL338066
- Wikipedia: Naringenin_chalcone
- Wikipedia: Naringenin chalcone
- LipidMAPS: LMPK12120264
- MeSH: naringenin chalcone
- ChemIDplus: 0073692509
- MetaCyc: CPD-20012
- KNApSAcK: C00007233
- foodb: FDB000801
- chemspider: 4444447
- CAS: 25515-46-2
- CAS: 5071-40-9
- MoNA: PB002406
- MoNA: PB000126
- MoNA: PB002405
- MoNA: PB000129
- MoNA: PB002408
- MoNA: PB000128
- MoNA: PB000127
- MoNA: PB002407
- medchemexpress: HY-N3007A
- medchemexpress: HY-N3007
- PMhub: MS000002798
- MetaboLights: MTBLC15413
- 3DMET: B00973
- NIKKAJI: J16.987K
- PubChem: 8790
- KNApSAcK: 15413
分类词条
相关代谢途径
Reactome(0)
代谢反应
322 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(10)
- aurone biosynthesis:
2',3,4,4',6'-pentahydroxychalcone 4'-O-β-D-glucoside + O2 ⟶ H2O + bracteatin 6-O-glucoside - flavonoid biosynthesis:
(2S)-naringenin + 2-oxoglutarate + O2 ⟶ (+)-dihydrokaempferol + CO2 + succinate - flavonoid di-C-glucosylation:
UDP-α-D-glucose + nothofagin ⟶ 3',5'-di-C-glucosylphloretin + H+ + UDP - naringenin biosynthesis (engineered):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
(+)-dihydrokaempferol + 2-oxoglutarate + O2 ⟶ CO2 + H+ + H2O + kaempferol + succinate - xanthohumol biosynthesis:
DMAPP + naringenin chalcone ⟶ H+ + desmethylxanthohumol + diphosphate - aromatic polyketides biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - chalcone 2'-O-glucoside biosynthesis:
UDP-α-D-glucose + naringenin chalcone ⟶ H+ + UDP + chalcone 2'-O-glucoside - flavonoid biosynthesis (in equisetum):
(2S)-naringenin + 2-oxoglutarate + O2 ⟶ (+)-dihydrokaempferol + CO2 + succinate - flavonoid biosynthesis:
(2S)-naringenin + 2-oxoglutarate + O2 ⟶ (+)-dihydrokaempferol + CO2 + succinate
Plant Reactome(0)
INOH(0)
PlantCyc(309)
- aurone biosynthesis:
2',3,4,4',6'-pentahydroxychalcone 4'-O-β-D-glucoside + O2 ⟶ H2O + aureusidin 6-O-glucoside - aurone biosynthesis:
O2 + butein 4'-β-D-glucoside ⟶ H2O + aureusidin 6-O-glucoside - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(2S)-naringenin + 2-oxoglutarate + O2 ⟶ (+)-dihydrokaempferol + CO2 + succinate - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH + malonyl-CoA ⟶ CO2 + H2O + NADP+ + coenzyme A + isoliquiritigenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH + malonyl-CoA ⟶ CO2 + H2O + NADP+ + coenzyme A + isoliquiritigenin - flavonoid di-C-glucosylation:
NADP+ + dihydro-4-coumaroyl-CoA ⟶ (E)-4-coumaroyl-CoA + H+ + NADPH - flavonoid biosynthesis (in equisetum):
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH + malonyl-CoA ⟶ CO2 + H2O + NADP+ + coenzyme A + isoliquiritigenin - flavonoid biosynthesis (in equisetum):
(2S)-eriodictyol + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ (2S)-dihydrotricetin + H2O + an oxidized [NADPH-hemoprotein reductase] - chalcone 2'-O-glucoside biosynthesis:
UDP-α-D-glucose + naringenin chalcone ⟶ H+ + UDP + chalcone 2'-O-glucoside - flavonoid biosynthesis (in equisetum):
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - naringenin biosynthesis (engineered):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
H+ + dihydro-4-coumaroyl-CoA + malonyl-CoA ⟶ CO2 + coenzyme A + phloretin - aromatic polyketides biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
(2S)-naringenin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ (2S)-eriodictyol + H+ + H2O + an oxidized [NADPH-hemoprotein reductase] - xanthohumol biosynthesis:
DMAPP + naringenin chalcone ⟶ H+ + desmethylxanthohumol + diphosphate - chalcone 2'-O-glucoside biosynthesis:
UDP-α-D-glucose + naringenin chalcone ⟶ H+ + UDP + chalcone 2'-O-glucoside - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH + malonyl-CoA ⟶ CO2 + H2O + NADP+ + coenzyme A + isoliquiritigenin - flavonoid biosynthesis (in equisetum):
naringenin chalcone ⟶ (2S)-naringenin - flavonoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid biosynthesis (in equisetum):
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - flavonoid di-C-glucosylation:
naringenin chalcone ⟶ (2S)-naringenin - flavonoid di-C-glucosylation:
(E)-4-coumaroyl-CoA + H+ + malonyl-CoA ⟶ CO2 + coenzyme A + naringenin chalcone - xanthohumol biosynthesis:
DMAPP + naringenin chalcone ⟶ H+ + desmethylxanthohumol + diphosphate
COVID-19 Disease Map(0)
PathBank(2)
- Flavanone Biosynthesis:
4-Hydroxycinnamic acid + Adenosine triphosphate + Coenzyme A ⟶ 4-Coumaroyl-CoA + Adenosine monophosphate + Pyrophosphate - Flavonoid Biosynthesis:
Hydrogen Ion + NADPH + Naringenin ⟶ Apiforol + NADP
PharmGKB(0)
26 个相关的物种来源信息
- 3702 - Arabidopsis thaliana: 10.1046/J.1365-313X.2003.01834.X
- 4686 - Asparagus officinalis: 10.1371/JOURNAL.PONE.0219973
- 38851 - Gentiana lutea: 10.1371/JOURNAL.PONE.0212062
- 3311 - Ginkgo biloba: 10.3389/FPLS.2019.00983
- 9606 - Homo sapiens: -
- 3486 - Humulus lupulus: 10.1021/JF1049084
- 35883 - Ipomoea nil: 10.1016/S0031-9422(00)90588-0
- 85856 - Magnolia denudata: 10.3390/MOLECULES23071558
- 3403 - Magnolia liliiflora: 10.3390/MOLECULES23071558
- 3724 - Matthiola incana: 10.1515/ZNC-1983-7-810
- 3673 - Momordica charantia: 10.3390/MOLECULES23020469
- 28933 - Nothofagus antarctica: 10.1515/ZNC-1979-1240
- 688333 - Populus cathayana: 10.1515/ZNC-1992-3-423
- 1085088 - Populus koreana: 10.1515/ZNC-1992-3-424
- 75703 - Populus maximowiczii: 10.1515/ZNC-1992-3-424
- 245546 - Populus suaveolens: 10.1515/ZNC-1992-3-424
- 179740 - Populus szechuanica: 10.1515/ZNC-1992-3-423
- 118781 - Populus tomentosa: 10.1016/0305-1978(91)90071-7
- 113636 - Populus tremula: 10.1016/0305-1978(91)90071-7
- 2900717 - Populus tremula var. sieboldii: 10.1016/0305-1978(91)90071-7
- 3693 - Populus tremuloides: 10.1016/0305-1978(91)90071-7
- 22663 - Punica granatum: 10.1371/JOURNAL.PONE.0142777
- 933138 - Salvia leucantha: 10.1016/S0040-4020(01)85654-4
- 2039553 - Salvia xalapensis: 10.1021/NP050041E
- 33090 - 枳实: -
- 569774 - 金线莲: -
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
- Ju Huang, Xin Zhao, Yan Zhang, Yao Chen, Ximin Zhang, Yin Yi, Zhigang Ju, Wei Sun. Chalcone-Synthase-Encoding RdCHS1 Is Involved in Flavonoid Biosynthesis in Rhododendron delavayi.
Molecules (Basel, Switzerland).
2024 Apr; 29(8):. doi:
10.3390/molecules29081822. [PMID: 38675642] - Yao Zhao, Jitao Hu, Yilin Zhang, Han Tao, Linying Li, Yuqing He, Xueying Zhang, Chi Zhang, Gaojie Hong. Unveiling targeted spatial metabolome of rice seed at the dough stage using Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry imaging.
Food research international (Ottawa, Ont.).
2023 Dec; 174(Pt 1):113578. doi:
10.1016/j.foodres.2023.113578. [PMID: 37986446] - Xin-Bo Cai, Nan Liu, Jia Li, Rong Liu, Yun-Feng Luo, Yi-Feng Zhang, Jia-Dian Wang, Xiao-Yi Wu, Lu-Qi Huang. [Functional characterization and enzymatic properties of flavonoid glycosyltransferase gene CtUGT49 in Carthamus tinctorius].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2023 Dec; 48(24):6624-6634. doi:
10.19540/j.cnki.cjcmm.20230809.101. [PMID: 38212022] - Emma R Wolf-Saxon, Chad C Moorman, Anthony Castro, Alfredo Ruiz, Jeremy P Mallari, Jason R Burke. Regulatory ligand binding in plant chalcone isomerase-like (CHIL) proteins.
The Journal of biological chemistry.
2023 May; ?(?):104804. doi:
10.1016/j.jbc.2023.104804. [PMID: 37172720] - Ana González Moreno, Jack M Woolley, Eva Domínguez, Abel de Cózar, Antonio Heredia, Vasilios G Stavros. Synergic photoprotection of phenolic compounds present in tomato fruit cuticle: a spectroscopic investigation in solution.
Physical chemistry chemical physics : PCCP.
2023 May; ?(?):. doi:
10.1039/d3cp00630a. [PMID: 37129056] - Hiraku Furudate, Misaki Manabe, Haruka Oshikiri, Ayako Matsushita, Bunta Watanabe, Toshiyuki Waki, Toru Nakayama, Hiroyoshi Kubo, Kojiro Takanashi. A Polyphenol Oxidase Catalyzes Aurone Synthesis in Marchantia polymorpha.
Plant & cell physiology.
2023 Mar; ?(?):. doi:
10.1093/pcp/pcad024. [PMID: 36947436] - Ana González Moreno, Eva Domínguez, Konrad Mayer, Nannan Xiao, Peter Bock, Antonio Heredia, Notburga Gierlinger. 3D (x-y-t) Raman imaging of tomato fruit cuticle: Microchemistry during development.
Plant physiology.
2023 01; 191(1):219-232. doi:
10.1093/plphys/kiac369. [PMID: 35972400] - Mengdi Zhang, Zhaoxin Wang, Siyu Hao, Lei Hao, Xinying Zhang, Peng Yu, Hua Sun. Synthesis of natural 3'-Prenylchalconaringenin and biological evaluation of ameliorating non-alcoholic fatty liver disease and metabolic syndrome.
European journal of medicinal chemistry.
2020 Nov; 205(?):112649. doi:
10.1016/j.ejmech.2020.112649. [PMID: 32791402] - Deze Kong, Sijin Li, Christina D Smolke. Discovery of a previously unknown biosynthetic capacity of naringenin chalcone synthase by heterologous expression of a tomato gene cluster in yeast.
Science advances.
2020 10; 6(44):. doi:
10.1126/sciadv.abd1143. [PMID: 33127687] - Carina Kolot, Ana Rodriguez-Mateos, Rodrigo Feliciano, Katharina Bottermann, Wilhelm Stahl. Bioavailability of naringenin chalcone in humans after ingestion of cherry tomatoes.
International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition.
2020 Oct; 90(5-6):411-416. doi:
10.1024/0300-9831/a000574. [PMID: 30961461] - Johann E Kufs, Sandra Hoefgen, Julia Rautschek, Alexander U Bissell, Carola Graf, Jonas Fiedler, Daniel Braga, Lars Regestein, Miriam A Rosenbaum, Julian Thiele, Vito Valiante. Rational Design of Flavonoid Production Routes Using Combinatorial and Precursor-Directed Biosynthesis.
ACS synthetic biology.
2020 07; 9(7):1823-1832. doi:
10.1021/acssynbio.0c00172. [PMID: 32525654] - Elvira Escribano-Ferrer, Josep Queralt Regué, Xavier Garcia-Sala, Antoni Boix Montañés, Rosa M Lamuela-Raventos. In Vivo Anti-inflammatory and Antiallergic Activity of Pure Naringenin, Naringenin Chalcone, and Quercetin in Mice.
Journal of natural products.
2019 02; 82(2):177-182. doi:
10.1021/acs.jnatprod.8b00366. [PMID: 30688453] - Miriam Kaltenbach, Jason R Burke, Mirco Dindo, Anna Pabis, Fabian S Munsberg, Avigayel Rabin, Shina C L Kamerlin, Joseph P Noel, Dan S Tawfik. Evolution of chalcone isomerase from a noncatalytic ancestor.
Nature chemical biology.
2018 06; 14(6):548-555. doi:
10.1038/s41589-018-0042-3. [PMID: 29686356] - Mosaab Yahyaa, Samah Ali, Rachel Davidovich-Rikanati, Muhammad Ibdah, Alona Shachtier, Yoram Eyal, Efraim Lewinsohn, Mwafaq Ibdah. Characterization of three chalcone synthase-like genes from apple (Malus x domestica Borkh.).
Phytochemistry.
2017 Aug; 140(?):125-133. doi:
10.1016/j.phytochem.2017.04.022. [PMID: 28482241] - Merve Tomas, Jules Beekwilder, Robert D Hall, Osman Sagdic, Dilek Boyacioglu, Esra Capanoglu. Industrial processing versus home processing of tomato sauce: Effects on phenolics, flavonoids and in vitro bioaccessibility of antioxidants.
Food chemistry.
2017 Apr; 220(?):51-58. doi:
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Journal of agricultural and food chemistry.
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Plant physiology.
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Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban.
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