phosphatidyl (3,5) inositol biphosphate
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phosphatidyl (3,5) inositol biphosphate
Summary
phosphatidyl (3,5) inositol biphosphate is a group of stereoisomers[1]. It draws 34 Wikipedia views per month (group_of_stereoisomers category, ranking #213 of 1,063).[2]
Key Facts
- phosphatidyl (3,5) inositol biphosphate's instance of is recorded as group of stereoisomers[3].
- phosphatidyl (3,5) inositol biphosphate's physically interacts with is recorded as Two pore segment channel 1[4].
- phosphatidyl (3,5) inositol biphosphate's physically interacts with is recorded as Two pore segment channel 2[5].
- phosphatidyl (3,5) inositol biphosphate's physically interacts with is recorded as Mucolipin 1[6].
- phosphatidyl (3,5) inositol biphosphate's canonical SMILES is recorded as CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)OC1C(C(C(C(C1O)OP(=O)(O)O)O)OP(=O)(O)O)O)OC(=O)CCCCCCCCCCCCCCC[7].
- phosphatidyl (3,5) inositol biphosphate's chemical formula is recorded as C₄₁H₈₁O₁₉P₃[8].
- phosphatidyl (3,5) inositol biphosphate is a type of primary metabolite[9].
- phosphatidyl (3,5) inositol biphosphate is part of phosphatidylinositol-3,5-bisphosphate binding[10].
- phosphatidyl (3,5) inositol biphosphate is part of 1-phosphatidylinositol-3-phosphate 5-kinase activity[11].
- phosphatidyl (3,5) inositol biphosphate is part of phosphatidylinositol-3,5-bisphosphate 3-phosphatase activity[12].
- phosphatidyl (3,5) inositol biphosphate is part of 1-phosphatidyl-1D-myo-inositol 3,5-bisphosphate metabolic process[13].
- phosphatidyl (3,5) inositol biphosphate is part of 1-phosphatidyl-1D-myo-inositol 3,5-bisphosphate catabolic process[14].
- phosphatidyl (3,5) inositol biphosphate is part of 1-phosphatidyl-1D-myo-inositol 3,5-bisphosphate biosynthetic process[15].
- phosphatidyl (3,5) inositol biphosphate's isomeric SMILES is recorded as CCCCCCCCCCCCCCCC(=O)OCC@HOC(=O)CCCCCCCCCCCCCCCC@HOC(=O)CCCCCCCCCCCCCCC">[16].
- phosphatidyl (3,5) inositol biphosphate's mass is recorded as {'unit': 'Q483261', 'amount': '+970.4584902620002'}[17].
Why It Matters
phosphatidyl (3,5) inositol biphosphate draws 34 Wikipedia views per month (group_of_stereoisomers category, ranking #213 of 1,063).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[18] It is known by 7 alternative names across languages and contexts.[19]