D-myo-Inositol 1,4-bisphosphate (BioDeep_00000001739)
Secondary id: BioDeep_00001869383
human metabolite PANOMIX_OTCML-2023 Endogenous
代谢物信息卡片
化学式: C6H14O12P2 (339.9961)
中文名称:
谱图信息:
最多检出来源 Homo sapiens(plant) 5.9%
分子结构信息
SMILES: C1(C(C(C(C(C1OP(=O)(O)O)O)O)OP(=O)(O)O)O)O
InChI: InChI=1S/C6H14O12P2/c7-1-2(8)6(18-20(14,15)16)4(10)3(9)5(1)17-19(11,12)13/h1-10H,(H2,11,12,13)(H2,14,15,16)/t1-,2-,3-,4+,5+,6+/m1/s1
描述信息
D-myo-Inositol 1,4-bisphosphate belongs to the class of organic compounds known as inositol phosphates. Inositol phosphates are compounds containing a phosphate group attached to an inositol (or cyclohexanehexol) moiety. D-myo-Inositol 1,4-bisphosphate is an extremely weak basic (essentially neutral) compound (based on its pKa). D-myo-Inositol 1,4-bisphosphate is a substrate for several proteins including inositol polyphosphate 1-phosphatase, phosphatidylinositol 4,5-bisphosphate 5-phosphatase A, skeletal muscle and kidney enriched inositol phosphatase, and type I inositol-1,4,5-trisphosphate 5-phosphatase.
1D-Myo-inositol 1,4-bisphosphate is a substrate for Inositol polyphosphate 1-phosphatase, Phosphatidylinositol 4,5-bisphosphate 5-phosphatase A, Skeletal muscle and kidney enriched inositol phosphatase and Type I inositol-1,4,5-trisphosphate 5-phosphatase. [HMDB]
同义名列表
14 个代谢物同义名
{[(1R,2R,3R,4R,5R,6S)-2,3,5,6-tetrahydroxy-4-(phosphonooxy)cyclohexyl]oxy}phosphonic acid; [(1R,2R,3R,4R,5R,6S)-2,3,5,6-tetrahydroxy-4-(phosphonooxy)cyclohexyl]oxyphosphonic acid; 1D-Myo-inositol 1,4-bisphosphoric acid; D-MYO-inositol-1,4-bisphosphoric acid; D-Myo-inositol 1,4-bisphosphoric acid; Myo-inositol 1,4-bisphosphoric acid; 1D-myo-inositol 1,4-bisphosphate; Inositol 1,4-bisphosphoric acid; D-MYO-inositol-1,4-bisphosphATE; D-myo-Inositol 1,4-bisphosphate; Myo-inositol 1,4-bisphosphate; Inositol 1,4-bisphosphate; Inositol 1,4-diphosphate; 1D-myo-Inositol 1,4-bisphosphate
数据库引用编号
19 个数据库交叉引用编号
- ChEBI: CHEBI:191032
- ChEBI: CHEBI:17816
- KEGG: C01220
- PubChem: 439444
- PubChem: 805
- HMDB: HMDB0000968
- Metlin: METLIN410
- DrugBank: DB03158
- MetaCyc: INOSITOL-1-4-BISPHOSPHATE
- KNApSAcK: C00007484
- foodb: FDB022343
- chemspider: 17216032
- CAS: 74465-19-3
- CAS: 47055-78-7
- PMhub: MS000001079
- PubChem: 4442
- 3DMET: B01411
- NIKKAJI: J281.780B
- KNApSAcK: 17816
分类词条
相关代谢途径
BioCyc(0)
PlantCyc(0)
代谢反应
69 个相关的代谢反应过程信息。
Reactome(54)
- Metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA
- Inositol phosphate metabolism:
ATP + I(3,4,5,6)P4 ⟶ ADP + I(1,3,4,5,6)P5
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-one-CoA + CoA-SH ⟶ choloyl-CoA + propionyl CoA
- Inositol phosphate metabolism:
H2O + I4P ⟶ Ins + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-one-CoA + CoA-SH ⟶ choloyl-CoA + propionyl CoA
- Inositol phosphate metabolism:
H2O + I4P ⟶ Ins + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Inositol phosphate metabolism:
H2O + I4P ⟶ Ins + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Inositol phosphate metabolism:
H2O + I4P ⟶ Ins + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
ATP + PROP-CoA + carbon dioxide ⟶ ADP + MEMA-CoA + Pi
- Inositol phosphate metabolism:
H2O + I4P ⟶ Ins + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Inositol phosphate metabolism:
H2O + I4P ⟶ Ins + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA
- Inositol phosphate metabolism:
H2O + I4P ⟶ Ins + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-one-CoA + CoA-SH ⟶ choloyl-CoA + propionyl CoA
- Inositol phosphate metabolism:
H2O + I4P ⟶ Ins + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Inositol phosphate metabolism:
H2O + I4P ⟶ Ins + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA
- Inositol phosphate metabolism:
ATP + I(1,3,4)P3 ⟶ ADP + I(1,3,4,5)P4
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA
- Inositol phosphate metabolism:
H2O + I(1,4,5)P3 ⟶ I(1,4)P2 + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I(1,4,5)P3 ⟶ I(1,4)P2 + Pi
- Metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA
- Inositol phosphate metabolism:
H2O + I4P ⟶ Ins + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
CAR + propionyl CoA ⟶ CoA-SH + Propionylcarnitine
- Inositol phosphate metabolism:
H2O + I4P ⟶ Ins + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
GAA + SAM ⟶ CRET + H+ + SAH
- Inositol phosphate metabolism:
H2O + I(1,4,5)P3 ⟶ I(1,4)P2 + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I(1,4,5)P3 ⟶ I(1,4)P2 + Pi
- Metabolism:
ATP + PROP-CoA + carbon dioxide ⟶ ADP + MEMA-CoA + Pi
- Inositol phosphate metabolism:
H2O + I(1,4,5)P3 ⟶ I(1,4)P2 + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I(1,4,5)P3 ⟶ I(1,4)P2 + Pi
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Inositol phosphate metabolism:
H2O + I4P ⟶ Ins + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Inositol phosphate metabolism:
H2O + I4P ⟶ Ins + Pi
- Synthesis of IP2, IP, and Ins in the cytosol:
H2O + I4P ⟶ Ins + Pi
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(1)
- Inositol phosphate metabolism ( Inositol phosphate metabolism ):
O2 + myo-Inositol ⟶ D-Glucuronic acid + H2O
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(14)
- Inositol Metabolism:
Oxygen + myo-Inositol ⟶ D-Glucuronic acid + Water
- Inositol Phosphate Metabolism:
1D-myo-Inositol 3-phosphate + Water ⟶ Phosphate + myo-Inositol
- Inositol Phosphate Metabolism:
Myo-inositol 1-phosphate + Water ⟶ Phosphate + myo-Inositol
- Inositol Metabolism:
Myo-inositol 1-phosphate + Water ⟶ Phosphate + myo-Inositol
- Inositol Metabolism:
Oxygen + myo-Inositol ⟶ D-Glucuronic acid + Water
- Inositol Phosphate Metabolism:
Myo-inositol 1-phosphate + Water ⟶ Phosphate + myo-Inositol
- Inositol Metabolism:
Oxygen + myo-Inositol ⟶ D-Glucuronic acid + Water
- Inositol Phosphate Metabolism:
Myo-inositol 1-phosphate + Water ⟶ Phosphate + myo-Inositol
- Inositol Metabolism:
Oxygen + myo-Inositol ⟶ D-Glucuronic acid + Water
- Inositol Phosphate Metabolism:
Myo-inositol 1-phosphate + Water ⟶ Phosphate + myo-Inositol
- Inositol Metabolism:
Oxygen + myo-Inositol ⟶ D-Glucuronic acid + Water
- Inositol Phosphate Metabolism:
Myo-inositol 1-phosphate + Water ⟶ Phosphate + myo-Inositol
- Inositol Metabolism:
Oxygen + myo-Inositol ⟶ D-Glucuronic acid + Water
- Inositol Phosphate Metabolism:
Myo-inositol 1-phosphate + Water ⟶ Phosphate + myo-Inositol
PharmGKB(0)
1 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。
文献列表
- Ju He, Joanna Gajewiak, Jordan L Scott, Denghuang Gong, Muzaffar Ali, Michael D Best, Glenn D Prestwich, Robert V Stahelin, Tatiana G Kutateladze. Metabolically stabilized derivatives of phosphatidylinositol 4-phosphate: synthesis and applications.
Chemistry & biology.
2011 Oct; 18(10):1312-9. doi:
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Developmental cell.
2011 Jun; 20(6):855-66. doi:
10.1016/j.devcel.2011.05.013
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PloS one.
2011 Feb; 6(2):e16724. doi:
10.1371/journal.pone.0016724
. [PMID: 21304819] - Florian Vogel, Daniel Hofius, Kathrin Elisabeth Paulus, Isabel Jungkunz, Uwe Sonnewald. The second face of a known player: Arabidopsis silencing suppressor AtXRN4 acts organ-specifically.
The New phytologist.
2011 Jan; 189(2):484-93. doi:
10.1111/j.1469-8137.2010.03482.x
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PLoS pathogens.
2010 May; 6(5):e1000909. doi:
10.1371/journal.ppat.1000909
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Journal of mental health (Abingdon, England).
2010 Apr; 19(2):142-56. doi:
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Plant physiology.
2010 Mar; 152(3):1357-72. doi:
10.1104/pp.109.149369
. [PMID: 20044451] - Víctor M Rodríguez, Aurore Chételat, Paul Majcherczyk, Edward E Farmer. Chloroplastic phosphoadenosine phosphosulfate metabolism regulates basal levels of the prohormone jasmonic acid in Arabidopsis leaves.
Plant physiology.
2010 Mar; 152(3):1335-45. doi:
10.1104/pp.109.150474
. [PMID: 20053710] - Ivan Ivetac, Rajendra Gurung, Sandra Hakim, Kristy A Horan, David A Sheffield, Lauren C Binge, Philip W Majerus, Tony Tiganis, Christina A Mitchell. Regulation of PI(3)K/Akt signalling and cellular transformation by inositol polyphosphate 4-phosphatase-1.
EMBO reports.
2009 May; 10(5):487-93. doi:
10.1038/embor.2009.28
. [PMID: 19325558] - Andreas Knödler, Gerlinde Konrad, Peter Mayinger. Expression of yeast lipid phosphatase Sac1p is regulated by phosphatidylinositol-4-phosphate.
BMC molecular biology.
2008 Jan; 9(?):16. doi:
10.1186/1471-2199-9-16
. [PMID: 18226253] - Leandro Michelon, Ivanor Meira-Lima, Quirino Cordeiro, Karen Miguita, Gerome Breen, David Collier, Homero Vallada. Association study of the INPP1, 5HTT, BDNF, AP-2beta and GSK-3beta GENE variants and restrospectively scored response to lithium prophylaxis in bipolar disorder.
Neuroscience letters.
2006 Aug; 403(3):288-93. doi:
10.1016/j.neulet.2006.05.001
. [PMID: 16787706] - John F Andersen, José M C Ribeiro. A secreted salivary inositol polyphosphate 5-phosphatase from a blood-feeding insect: allosteric activation by soluble phosphoinositides and phosphatidylserine.
Biochemistry.
2006 May; 45(17):5450-7. doi:
10.1021/bi052444j
. [PMID: 16634626] - Liming Xiong, Hojoung Lee, Rongfeng Huang, Jian-Kang Zhu. A single amino acid substitution in the Arabidopsis FIERY1/HOS2 protein confers cold signaling specificity and lithium tolerance.
The Plant journal : for cell and molecular biology.
2004 Nov; 40(4):536-45. doi:
10.1111/j.1365-313x.2004.02225.x
. [PMID: 15500469] - Masaru Yamakoshi, Mamoru Takahashi, Takuji Kouzuma, Shigeyuki Imamura, Isami Tsuboi, Shoji Kawazu, Fumio Yamagata, Makoto Tominaga, Masayuki Noritake. Determination of urinary myo-inositol concentration by an improved enzymatic cycling method using myo-inositol dehydrogenase from Flavobacterium sp.
Clinica chimica acta; international journal of clinical chemistry.
2003 Feb; 328(1-2):163-71. doi:
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Psychiatric genetics.
2002 Mar; 12(1):23-7. doi:
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Current biology : CB.
2001 Nov; 11(23):R968-70. doi:
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Genes & development.
2001 Aug; 15(15):1971-84. doi:
10.1101/gad.891901
. [PMID: 11485991] - A J Smith, Z Surviladze, E A Gaudet, J M Backer, C A Mitchell, B S Wilson. p110beta and p110delta phosphatidylinositol 3-kinases up-regulate Fc(epsilon)RI-activated Ca2+ influx by enhancing inositol 1,4,5-trisphosphate production.
The Journal of biological chemistry.
2001 May; 276(20):17213-20. doi:
10.1074/jbc.m100417200
. [PMID: 11279065] - Y Tsujishita, S Guo, L E Stolz, J D York, J H Hurley. Specificity determinants in phosphoinositide dephosphorylation: crystal structure of an archetypal inositol polyphosphate 5-phosphatase.
Cell.
2001 May; 105(3):379-89. doi:
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. [PMID: 11348594] - B D Spiegelberg, J P Xiong, J J Smith, R F Gu, J D York. Cloning and characterization of a mammalian lithium-sensitive bisphosphate 3'-nucleotidase inhibited by inositol 1,4-bisphosphate.
The Journal of biological chemistry.
1999 May; 274(19):13619-28. doi:
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Journal of lipid mediators.
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"
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Cell biochemistry and function.
1993 Mar; 11(1):55-62. doi:
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. [PMID: 8453737] - M G Thompson, J A Hickman. Doxorubicin interactions at the membrane: evidence for a biphasic modulation of inositol lipid metabolism.
European journal of cancer (Oxford, England : 1990).
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The Biochemical journal.
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. [PMID: 2850797] - G Guillemette, T Balla, A J Baukal, A Spät, K J Catt. Intracellular receptors for inositol 1,4,5-trisphosphate in angiotensin II target tissues.
The Journal of biological chemistry.
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The Journal of biological chemistry.
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