Dolichol monophosphate mannose

Base Information

• Chemical Name: Dolichol monophosphate mannose
• CAS No.: 55598-56-6
• Molecular Formula: C106H175O9P
• Molecular Weight: 1624.492061
• Wikipedia: Dolichol_monophosphate_mannose
• Wikidata: Q5289052
• Mol file: 55598-56-6.mol

Synonyms:Alpha-D-Mannopyranosyl Phosphate, Dolichyl;D Mannopyranosyldolichyl;D-Mannopyranosyldolichyl;Dolichol Monophosphate Mannose;Dolichol, Mannosyl Phosphoryl;Dolicholphosphate Mannose;Dolichyl Alpha D Mannopyranosyl Phosphate;Dolichyl Alpha-D-Mannopyranosyl Phosphate;Dolichyl Mannopyranosyl Phosphate;Dolichyl Mannosyl Phosphate;Mannolipid;Mannopyranosyl Phosphate, Dolichyl;Mannose, Dolichol Monophosphate;Mannose, Dolicholphosphate;Mannosyl Phosphate, Dolichyl;Mannosyl Phosphoryl Dolichol;Monophosphate Mannose, Dolichol;Phosphate, Dolichyl Alpha-D-Mannopyranosyl;Phosphate, Dolichyl Mannopyranosyl;Phosphate, Dolichyl Mannosyl;Phosphoryl Dolichol, Mannosyl

Chemical Property of Dolichol monophosphate mannose

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: g/cm³
• XLogP3: 33.9
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 64
• Exact Mass: 1624.30072899
• Heavy Atom Count: 116
• Complexity: 3410

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
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MSDS Files:

Useful:

• Canonical SMILES: CC(CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C)CCOP(=O)(O)OC1C(C(C(C(O1)CO)O)O)O
• Isomeric SMILES: CC(CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CCC=C(C)C)CCOP(=O)(O)O[C@H]1[C@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
• Use Description: Dolichol monophosphate mannose (Dol-P-Man) is a critical molecule with distinct roles in various fields. In the field of biochemistry and cell biology, it is essential for the process of N-glycosylation, a crucial post-translational modification of proteins in the endoplasmic reticulum (ER). Dol-P-Man acts as a carrier of mannose residues, facilitating the attachment of mannose to newly synthesized proteins, which is essential for their proper folding and function. In the realm of glycobiology and pharmaceuticals, understanding Dol-P-Man's role is vital for studying glycosylation disorders and developing therapies targeting this pathway. Additionally, in agriculture and biotechnology, it can be used to engineer glycoproteins in plants or microbial systems for the production of therapeutic proteins and vaccines. Its multifaceted utility underscores its importance in advancing cellular biology, medicine, and biotechnology, where it plays a pivotal role in protein modification, disease research, and biopharmaceutical production.