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Catalog Number | ACM60755808-1 |
CAS Number | 60755-80-8 |
Synonyms | O-Desmethylgalantamine |
Molecular Weight | 273.33 |
InChI | InChI=1S/C16H19NO3/c1-17-7-6-16-5-4-11(18)8-13(16)20-15-12(19)3-2-10(9-17)14(15)16/h2-5,11,13,18-19H,6-9H2,1H3/t11-,13-,16-/m0/s1 |
InChI Key | OYSGWKOGUVOGFQ-RBOXIYTFSA-N |
Melting Point | 227-230 °C |
Purity | 90%+ |
Complexity | 426 |
Covalently-Bonded Unit Count | 1 |
Defined Atom Stereocenter Count | 3 |
Exact Mass | 273.13649347 |
Heavy Atom Count | 20 |
Hydrogen Bond Acceptor Count | 4 |
Hydrogen Bond Donor Count | 2 |
Isomeric SMILES | CN1CC[C@@]23C=C[C@@H](C[C@@H]2OC4=C(C=CC(=C34)C1)O)O |
Monoisotopic Mass | 273.13649347 |
PhysicalState | Powder |
Rotatable Bond Count | 0 |
Topological Polar Surface Area | 52.9 Ų |
What is the chemical name of the compound with the CAS number 60755-80-8?
The chemical name of the compound is O-DESMETHYLGALANTHAMINE.
What is the molecular formula of O-DESMETHYLGALANTHAMINE?
The molecular formula is C16H19NO3.
What is the melting point of O-DESMETHYLGALANTHAMINE?
The melting point is 227-230°C.
What is the main usage of O-DESMETHYLGALANTHAMINE?
It is a metabolite of Galanthamine, which is a selective acetylcholinesterase inhibitor.
How does Sanguinine differ from Galanthamine in terms of acetylcholinesterase inhibitory activity?
Sanguinine has a more potent acetylcholinesterase inhibitory activity than galanthamine due to an extra hydroxyl group available for potential interaction with acetylcholinesterase.
What is the storage temperature recommended for O-DESMETHYLGALANTHAMINE?
The storage temperature recommended is -20°C freezer.
What is the solubility of O-DESMETHYLGALANTHAMINE in DMSO?
It is soluble in DMSO.
What is the predicted pKa of O-DESMETHYLGALANTHAMINE?
The predicted pKa is 9.39±0.40.
What is the chemical property of Sanguinine?
Sanguinine is a pale yellow powder.
How does the acetylcholinesterase inhibitory activity of Sanguinine compare to that of lycoramine and epinorlicoramine?
Sanguinine is 10-fold more selective than galanthamine for acetylcholinesterase (AChE) vs. butyrylcholinesterase (BuChE), whereas lycoramine and epinorlicoramine lack AChE inhibitory activity.
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