Weight | 260.135 g/mol |
---|---|
Formula | C6H13O9P |
Hydrogen Acceptors | 7 |
Hydrogen Donors | 7 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
Inositol 3-phosphate (2831-74-5, 573-35-3)
Score:
#1930 in Biochemistry
,
#4101 in Biology
,
#5168 in Chemistry
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- Type I phosphatidylinositol kinase makes a novel inositol phospholipid, phosphatidylinositol-3-phosphate (Nature, 1988)
- Somatic mutations causing constitutive activity of the thyrotropin receptor are the major cause of hyperfunctioning thyroid adenomas: identification of additional mutations activating both the cyclic adenosine 3',5'-monophosphate and inositol phosphate-Ca2+ cascades. (Molecular Endocrinology, 1995)
- A recombinant calcitonin receptor independently stimulates 3',5'-cyclic adenosine monophosphate and Ca2+/inositol phosphate signaling pathways. (Molecular Endocrinology, 1992)
- Enantiodivergence in small-molecule catalysis of asymmetric phosphorylation: Concise total syntheses of the enantiomeric D-myo-inositol-1-phosphate and D-myo-inositol-3-phosphate (Journal of the American Chemical Society, 2002)
- Expression of d-myo-Inositol-3-Phosphate Synthase in Soybean. Implications for Phytic Acid Biosynthesis (Plant Physiology, 2001)
- Insulin-induced activation of glycerol-3-phosphate acyltransferase by a chiro-inositol-containing insulin mediator is defective in adipocytes of insulin-resistant, type II diabetic, Goto-Kakizaki rats (Proceedings of the National Academy of Sciences of the United States of America, 1994)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1(C(C(C(C(C1O)O)OP(=O)(O)O)O)O)O
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InChIKeyINAPMGSXUVUWAF-UHFFFAOYSA-N
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