5-Hydroxyconiferaldehyde (BioDeep_00000009171)
PANOMIX_OTCML-2023
代谢物信息卡片
5-Hydroxyconiferyl aldehyde
化学式: C10H10O4 (194.057906)
中文名称:
谱图信息:
最多检出来源 Viridiplantae(plant) 0.6%
分子结构信息
SMILES: c1c(c(c(cc1/C=C/C=O)OC)O)O
InChI: InChI=1S/C10H10O4/c1-14-9-6-7(3-2-4-11)5-8(12)10(9)13/h2-6,12-13H,1H3/b3-2+
数据库引用编号
16 个数据库交叉引用编号
- ChEBI: CHEBI:31134
- KEGG: C12204
- PubChem: 5282094
- PubChem: 443703
- Metlin: METLIN64178
- MetaCyc: 5-HYDROXY-CONIFERALDEHYDE
- KNApSAcK: C00052737
- KNApSAcK: C00007611
- CAS: 266999-89-7
- CAS: 249647-14-1
- PMhub: MS000022925
- PubChem: 14350
- 3DMET: B04444
- NIKKAJI: J1.181.065I
- NIKKAJI: J1.273.258I
- RefMet: 5-Hydroxyconiferaldehyde
分类词条
相关代谢途径
Reactome(0)
代谢反应
152 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(4)
- ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
5-hydroxy-coniferaldehyde + SAM ⟶ H+ + SAH + sinapaldehyde - phenylpropanoid biosynthesis:
5-hydroxy-coniferaldehyde + SAM ⟶ H+ + SAH + sinapaldehyde - ferulate and sinapate biosynthesis:
5-hydroxy-coniferaldehyde + SAM ⟶ H+ + SAH + sinapaldehyde
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(148)
- phenylpropanoid biosynthesis:
4-coumaryl alcohol + NADP+ ⟶ 4-coumaraldehyde + H+ + NADPH - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH ⟶ 4-coumaraldehyde + NADP+ + coenzyme A - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
trans-feruloyl-CoA + H+ + NADPH ⟶ NADP+ + coenzyme A + coniferaldehyde - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
NADP+ + sinapyl alcohol ⟶ H+ + NADPH + sinapaldehyde - phenylpropanoid biosynthesis:
4-coumaryl alcohol + NADP+ ⟶ 4-coumaraldehyde + H+ + NADPH - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
5-hydroxy-coniferaldehyde + SAM ⟶ H+ + SAH + sinapaldehyde - phenylpropanoid biosynthesis:
trans-feruloyl-CoA + H+ + NADPH ⟶ NADP+ + coenzyme A + coniferaldehyde - phenylpropanoid biosynthesis:
trans-feruloyl-CoA + H+ + NADPH ⟶ NADP+ + coenzyme A + coniferaldehyde - phenylpropanoid biosynthesis:
H+ + NADPH + feruloyl-CoA ⟶ NADP+ + coenzyme A + coniferaldehyde - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
NADP+ + coniferyl alcohol ⟶ H+ + NADPH + coniferaldehyde - phenylpropanoid biosynthesis:
4-coumaryl alcohol + NADP+ ⟶ 4-coumaraldehyde + H+ + NADPH - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH ⟶ 4-coumaraldehyde + NADP+ + coenzyme A - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
NADP+ + sinapyl alcohol ⟶ H+ + NADPH + sinapaldehyde - phenylpropanoid biosynthesis:
NADP+ + coniferyl alcohol ⟶ H+ + NADPH + coniferaldehyde - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
NADP+ + sinapyl alcohol ⟶ H+ + NADPH + sinapaldehyde - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
NADP+ + coniferyl alcohol ⟶ H+ + NADPH + coniferaldehyde - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
NADP+ + coniferyl alcohol ⟶ H+ + NADPH + coniferaldehyde - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH ⟶ 4-coumaraldehyde + NADP+ + coenzyme A - phenylpropanoid biosynthesis:
4-coumaryl alcohol + NADP+ ⟶ 4-coumaraldehyde + H+ + NADPH - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH ⟶ 4-coumaraldehyde + NADP+ + coenzyme A - phenylpropanoid biosynthesis:
4-coumaryl alcohol + NADP+ ⟶ 4-coumaraldehyde + H+ + NADPH - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
H+ + NADPH + feruloyl-CoA ⟶ NADP+ + coenzyme A + coniferaldehyde - phenylpropanoid biosynthesis:
NADP+ + coniferyl alcohol ⟶ H+ + NADPH + coniferaldehyde - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
NADP+ + coniferyl alcohol ⟶ H+ + NADPH + coniferaldehyde - phenylpropanoid biosynthesis:
4-coumaryl alcohol + NADP+ ⟶ 4-coumaraldehyde + H+ + NADPH - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH ⟶ 4-coumaraldehyde + NADP+ + coenzyme A - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
H+ + NADPH + feruloyl-CoA ⟶ NADP+ + coenzyme A + coniferaldehyde - phenylpropanoid biosynthesis:
4-coumaryl alcohol + NADP+ ⟶ 4-coumaraldehyde + H+ + NADPH - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH ⟶ 4-coumaraldehyde + NADP+ + coenzyme A - phenylpropanoid biosynthesis:
4-coumaryl alcohol + NADP+ ⟶ 4-coumaraldehyde + H+ + NADPH - phenylpropanoid biosynthesis:
trans-feruloyl-CoA + H+ + NADPH ⟶ NADP+ + coenzyme A + coniferaldehyde - phenylpropanoid biosynthesis:
trans-feruloyl-CoA + H+ + NADPH ⟶ NADP+ + coenzyme A + coniferaldehyde - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
trans-feruloyl-CoA + H+ + NADPH ⟶ NADP+ + coenzyme A + coniferaldehyde - phenylpropanoid biosynthesis:
trans-feruloyl-CoA + H+ + NADPH ⟶ NADP+ + coenzyme A + coniferaldehyde - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH ⟶ 4-coumaraldehyde + NADP+ + coenzyme A - phenylpropanoid biosynthesis:
4-coumaryl alcohol + NADP+ ⟶ 4-coumaraldehyde + H+ + NADPH - phenylpropanoid biosynthesis:
NADP+ + sinapyl alcohol ⟶ H+ + NADPH + sinapaldehyde - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH ⟶ 4-coumaraldehyde + NADP+ + coenzyme A - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
trans-feruloyl-CoA + H+ + NADPH ⟶ NADP+ + coenzyme A + coniferaldehyde - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH ⟶ 4-coumaraldehyde + NADP+ + coenzyme A - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
H+ + NADPH + feruloyl-CoA ⟶ NADP+ + coenzyme A + coniferaldehyde - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
trans-feruloyl-CoA + H+ + NADPH ⟶ NADP+ + coenzyme A + coniferaldehyde - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
NADP+ + coniferyl alcohol ⟶ H+ + NADPH + coniferaldehyde - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
trans-feruloyl-CoA + H+ + NADPH ⟶ NADP+ + coenzyme A + coniferaldehyde - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
H+ + NADPH + feruloyl-CoA ⟶ NADP+ + coenzyme A + coniferaldehyde - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + H+ + NADPH ⟶ 4-coumaraldehyde + NADP+ + coenzyme A - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
trans-feruloyl-CoA + H+ + NADPH ⟶ NADP+ + coenzyme A + coniferaldehyde - phenylpropanoid biosynthesis:
4-coumaryl alcohol + NADP+ ⟶ 4-coumaraldehyde + H+ + NADPH - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
trans-feruloyl-CoA + H+ + NADPH ⟶ NADP+ + coenzyme A + coniferaldehyde - phenylpropanoid biosynthesis:
H+ + NADPH + feruloyl-CoA ⟶ NADP+ + coenzyme A + coniferaldehyde - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
5-hydroxy-coniferaldehyde + SAM ⟶ H+ + SAH + sinapaldehyde - ferulate and sinapate biosynthesis:
5-hydroxy-coniferaldehyde + SAM ⟶ H+ + SAH + sinapaldehyde - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - ferulate and sinapate biosynthesis:
H+ + NADPH + O2 + coniferaldehyde ⟶ 5-hydroxy-coniferaldehyde + H2O + NADP+ - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
NADP+ + sinapyl alcohol ⟶ H+ + NADPH + sinapaldehyde - ferulate and sinapate biosynthesis:
H2O + NADP+ + sinapaldehyde ⟶ H+ + NADPH + sinapate - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
(E)-4-coumaroyl-CoA + L-quinate ⟶ trans-5-O-(4-coumaroyl)-D-quinate + coenzyme A - phenylpropanoid biosynthesis:
trans-5-O-caffeoyl-D-quinate + coenzyme A ⟶ trans-caffeoyl-CoA + L-quinate - phenylpropanoid biosynthesis:
H+ + NADPH + feruloyl-CoA ⟶ NADP+ + coenzyme A + coniferaldehyde
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
4 个相关的物种来源信息
- 2753873 Daphne feddei: 10.1021/NP8004166
- 2753873 Daphne feddei: 10.1021/NP8004166
- 2753873 Daphne feddei: 10.1021/NP8004166
- 2753873 Daphne feddei: 10.1021/NP8004166
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
- Suk Weon Kim, Hye Jin Kim, Jong Hyun Kim, Yong Kook Kwon, Myung Suk Ahn, Young Pyo Jang, Jang R Liu. A rapid, simple method for the genetic discrimination of intact Arabidopsis thaliana mutant seeds using metabolic profiling by direct analysis in real-time mass spectrometry.
Plant methods.
2011 Jun; 7(?):14. doi:
10.1186/1746-4811-7-14. [PMID: 21658279] - Yun Lee, Fang Chen, Lina Gallego-Giraldo, Richard A Dixon, Eberhard O Voit. Integrative analysis of transgenic alfalfa (Medicago sativa L.) suggests new metabolic control mechanisms for monolignol biosynthesis.
PLoS computational biology.
2011 May; 7(5):e1002047. doi:
10.1371/journal.pcbi.1002047. [PMID: 21625579] - Gordon V Louie, Marianne E Bowman, Yi Tu, Aidyn Mouradov, German Spangenberg, Joseph P Noel. Structure-function analyses of a caffeic acid O-methyltransferase from perennial ryegrass reveal the molecular basis for substrate preference.
The Plant cell.
2010 Dec; 22(12):4114-27. doi:
10.1105/tpc.110.077578. [PMID: 21177481] - Fachuang Lu, Jane M Marita, Catherine Lapierre, Lise Jouanin, Kris Morreel, Wout Boerjan, John Ralph. Sequencing around 5-hydroxyconiferyl alcohol-derived units in caffeic acid O-methyltransferase-deficient poplar lignins.
Plant physiology.
2010 Jun; 153(2):569-79. doi:
10.1104/pp.110.154278. [PMID: 20427467] - Zhanyou Xu, Dandan Zhang, Jun Hu, Xin Zhou, Xia Ye, Kristen L Reichel, Nathan R Stewart, Ryan D Syrenne, Xiaohan Yang, Peng Gao, Weibing Shi, Crissa Doeppke, Robert W Sykes, Jason N Burris, Joseph J Bozell, Max Zong-Ming Cheng, Douglas G Hayes, Nicole Labbe, Mark Davis, C Neal Stewart, Joshua S Yuan. Comparative genome analysis of lignin biosynthesis gene families across the plant kingdom.
BMC bioinformatics.
2009 Oct; 10 Suppl 11(?):S3. doi:
10.1186/1471-2105-10-s11-s3. [PMID: 19811687] - Suvi Sutela, Karoliina Niemi, Jaanika Edesi, Tapio Laakso, Pekka Saranpää, Jaana Vuosku, Riina Mäkelä, Heidi Tiimonen, Vincent L Chiang, Janne Koskimäki, Marja Suorsa, Riitta Julkunen-Tiitto, Hely Häggman. Phenolic compounds in ectomycorrhizal interaction of lignin modified silver birch.
BMC plant biology.
2009 Sep; 9(?):124. doi:
10.1186/1471-2229-9-124. [PMID: 19788757] - Abdelali Barakat, Agnieszka Bagniewska-Zadworna, Alex Choi, Urmila Plakkat, Denis S DiLoreto, Priyadarshini Yellanki, John E Carlson. The cinnamyl alcohol dehydrogenase gene family in Populus: phylogeny, organization, and expression.
BMC plant biology.
2009 Mar; 9(?):26. doi:
10.1186/1471-2229-9-26. [PMID: 19267902] - Arnaud Day, Godfrey Neutelings, Frédérique Nolin, Sébastien Grec, Anouk Habrant, David Crônier, Bouchra Maher, Christian Rolando, Hélène David, Brigitte Chabbert, Simon Hawkins. Caffeoyl coenzyme A O-methyltransferase down-regulation is associated with modifications in lignin and cell-wall architecture in flax secondary xylem.
Plant physiology and biochemistry : PPB.
2009 Jan; 47(1):9-19. doi:
10.1016/j.plaphy.2008.09.011. [PMID: 19004632] - Michaël Quentin, Valérie Allasia, Anthony Pegard, Florent Allais, Paul-Henri Ducrot, Bruno Favery, Caroline Levis, Sophie Martinet, Clarissa Masur, Michel Ponchet, Dominique Roby, Nikolaus L Schlaich, Lise Jouanin, Harald Keller. Imbalanced lignin biosynthesis promotes the sexual reproduction of homothallic oomycete pathogens.
PLoS pathogens.
2009 Jan; 5(1):e1000264. doi:
10.1371/journal.ppat.1000264. [PMID: 19148278] - Sabine Guillaumie, Deborah Goffner, Odile Barbier, Jean-Pierre Martinant, Magalie Pichon, Yves Barrière. Expression of cell wall related genes in basal and ear internodes of silking brown-midrib-3, caffeic acid O-methyltransferase (COMT) down-regulated, and normal maize plants.
BMC plant biology.
2008 Jun; 8(?):71. doi:
10.1186/1471-2229-8-71. [PMID: 18582385] - Qing-Hu Ma, Yang Xu. Characterization of a caffeic acid 3-O-methyltransferase from wheat and its function in lignin biosynthesis.
Biochimie.
2008 Mar; 90(3):515-24. doi:
10.1016/j.biochi.2007.09.016. [PMID: 17976886] - Kris Morreel, John Ralph, Fachuang Lu, Geert Goeminne, Roger Busson, Piet Herdewijn, Jan L Goeman, Johan Van der Eycken, Wout Boerjan, Eric Messens. Phenolic profiling of caffeic acid O-methyltransferase-deficient poplar reveals novel benzodioxane oligolignols.
Plant physiology.
2004 Dec; 136(4):4023-36. doi:
10.1104/pp.104.049312. [PMID: 15563622] - Dianjing Guo, Fang Chen, Richard A Dixon. Monolignol biosynthesis in microsomal preparations from lignifying stems of alfalfa (Medicago sativa L.).
Phytochemistry.
2002 Nov; 61(6):657-67. doi:
10.1016/s0031-9422(02)00375-8. [PMID: 12423886] - Chloe Zubieta, Parvathi Kota, Jean-Luc Ferrer, Richard A Dixon, Joseph P Noel. Structural basis for the modulation of lignin monomer methylation by caffeic acid/5-hydroxyferulic acid 3/5-O-methyltransferase.
The Plant cell.
2002 Jun; 14(6):1265-77. doi:
10.1105/tpc.001412. [PMID: 12084826] - K Parvathi, F Chen, D Guo, J W Blount, R A Dixon. Substrate preferences of O-methyltransferases in alfalfa suggest new pathways for 3-O-methylation of monolignols.
The Plant journal : for cell and molecular biology.
2001 Jan; 25(2):193-202. doi:
10.1046/j.1365-313x.2001.00956.x. [PMID: 11169195]