{[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-({[hydroxy({hydroxy[3-hydroxy-3-({2-[(2-{[(3R)-3-hydroxybutanoyl]sulfanyl}ethyl)carbamoyl]ethyl}carbamoyl)-2,2-dimethylpropoxy]phosphoryl}oxy)phosphoryl]oxy}methyl)oxolan-3-yl]oxy}phosphonic acid (BioDeep_00001104028)
代谢物信息卡片
化学式: C25H42N7O18P3S (853.1519822000001)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC(CC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=NC3=C(N=CN=C32)N)O)OP(=O)(O)O)O)O
InChI: InChI=1S/C25H42N7O18P3S/c1-13(33)8-16(35)54-7-6-27-15(34)4-5-28-23(38)20(37)25(2,3)10-47-53(44,45)50-52(42,43)46-9-14-19(49-51(39,40)41)18(36)24(48-14)32-12-31-17-21(26)29-11-30-22(17)32/h11-14,18-20,24,33,36-37H,4-10H2,1-3H3,(H,27,34)(H,28,38)(H,42,43)(H,44,45)(H2,26,29,30)(H2,39,40,41)/t13-,14-,18-,19-,20?,24-/m1/s1
相关代谢途径
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代谢反应
71 个相关的代谢反应过程信息。
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PathBank(71)
- Lysine Degradation:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Fatty Acid Metabolism:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Butyrate Metabolism:
Adenosine triphosphate + Butyric acid + Coenzyme A ⟶ Adenosine monophosphate + Butyryl-CoA + Pyrophosphate
- Ethylmalonic Encephalopathy:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Glutaric Aciduria Type I:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency):
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Glutaric Aciduria Type I:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Saccharopinuria/Hyperlysinemia II:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids:
Adenosine triphosphate + Caproic acid + Coenzyme A ⟶ Adenosine monophosphate + Hexanoyl-CoA + Pyrophosphate
- Hyperlysinemia I, Familial:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Hyperlysinemia II or Saccharopinuria:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Carnitine Palmitoyl Transferase Deficiency I:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Long Chain Acyl-CoA Dehydrogenase Deficiency (LCAD):
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD):
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Carnitine Palmitoyl Transferase Deficiency II:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD):
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Trifunctional Protein Deficiency:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Short-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (SCHAD):
Adenosine triphosphate + Caproic acid + Coenzyme A ⟶ Adenosine monophosphate + Hexanoyl-CoA + Pyrophosphate
- Pyridoxine Dependency with Seizures:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- 2-Aminoadipic 2-Oxoadipic Aciduria:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- fatty acid oxidation (Butanoate):
Adenosine triphosphate + Butyric acid + Coenzyme A ⟶ Adenosine triphosphate + Butyryl-CoA
- Fatty Acid Metabolism:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Lysine Metabolism:
Hydrogen Ion + meso-diaminopimelate ⟶ Carbon dioxide + L-Lysine
- Fatty Acid Metabolism:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Butyrate Metabolism:
Adenosine triphosphate + Butyric acid + Coenzyme A ⟶ Adenosine monophosphate + Butyryl-CoA + Pyrophosphate
- Lysine Degradation:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids:
Adenosine triphosphate + Caproic acid + Coenzyme A ⟶ Adenosine monophosphate + Hexanoyl-CoA + Pyrophosphate
- 2-Aminoadipic 2-Oxoadipic Aciduria:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Ethylmalonic Encephalopathy:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Glutaric Aciduria Type I:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency):
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Saccharopinuria/Hyperlysinemia II:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Hyperlysinemia I, Familial:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Hyperlysinemia II or Saccharopinuria:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Carnitine Palmitoyl Transferase Deficiency I:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Long Chain Acyl-CoA Dehydrogenase Deficiency (LCAD):
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD):
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Carnitine Palmitoyl Transferase Deficiency II:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD):
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Trifunctional Protein Deficiency:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Short-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (SCHAD):
Adenosine triphosphate + Caproic acid + Coenzyme A ⟶ Adenosine monophosphate + Hexanoyl-CoA + Pyrophosphate
- Pyridoxine Dependency with Seizures:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- 2-Aminoadipic 2-Oxoadipic Aciduria:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Fatty Acid Metabolism:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Butyrate Metabolism:
Adenosine triphosphate + Butyric acid + Coenzyme A ⟶ Adenosine monophosphate + Butyryl-CoA + Pyrophosphate
- Lysine Degradation:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids:
Adenosine triphosphate + Caproic acid + Coenzyme A ⟶ Adenosine monophosphate + Hexanoyl-CoA + Pyrophosphate
- Fatty Acid Metabolism:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Butyrate Metabolism:
Adenosine triphosphate + Butyric acid + Coenzyme A ⟶ Adenosine monophosphate + Butyryl-CoA + Pyrophosphate
- Lysine Degradation:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids:
Adenosine triphosphate + Caproic acid + Coenzyme A ⟶ Adenosine monophosphate + Hexanoyl-CoA + Pyrophosphate
- Fatty Acid Metabolism:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids:
Adenosine triphosphate + Caproic acid + Coenzyme A ⟶ Adenosine monophosphate + Hexanoyl-CoA + Pyrophosphate
- Fatty Acid Metabolism:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids:
Adenosine triphosphate + Caproic acid + Coenzyme A ⟶ Adenosine monophosphate + Hexanoyl-CoA + Pyrophosphate
- Ethylmalonic Encephalopathy:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Glutaric Aciduria Type I:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency):
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Saccharopinuria/Hyperlysinemia II:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Hyperlysinemia I, Familial:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Hyperlysinemia II or Saccharopinuria:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Carnitine Palmitoyl Transferase Deficiency I:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Long Chain Acyl-CoA Dehydrogenase Deficiency (LCAD):
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD):
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Carnitine Palmitoyl Transferase Deficiency II:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD):
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Trifunctional Protein Deficiency:
Adenosine triphosphate + Coenzyme A + Palmitic acid ⟶ Adenosine monophosphate + Palmityl-CoA + Pyrophosphate
- Short-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (SCHAD):
Adenosine triphosphate + Caproic acid + Coenzyme A ⟶ Adenosine monophosphate + Hexanoyl-CoA + Pyrophosphate
- Pyridoxine Dependency with Seizures:
L-Lysine + NADPH + Oxoglutaric acid ⟶ NADP + Saccharopine + Water
- Fatty Acid Oxidation (Butanoate):
Adenosine triphosphate + Butyric acid + Coenzyme A ⟶ Adenosine monophosphate + Butyryl-CoA
- Butanoate Metabolism:
3-Hydroxy-3-methylglutaryl-CoA ⟶ Acetoacetic acid + Acetyl-CoA
PharmGKB(0)
0 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。