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ChemicalBook--->CAS DataBase List--->71294-60-5

71294-60-5

71294-60-5 Structure

71294-60-5 Structure
IdentificationBack Directory
[Name]

ROHITUKINE
[CAS]

71294-60-5
[Synonyms]

NSC623611
NSC-623611
NSC 623611
ROHITUKINE
5,7-dihydroxy-8-[(3S,4R)-3-hydroxy-1-methylpiperidin-4-yl]-2-methylchromen-4-one
5,7-Dihydroxy-8-[(3S,4R)-3-hydroxy-1-methyl-4-piperidinyl]-2-methyl-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one, 5,7-dihydroxy-8-[(3S,4R)-3-hydroxy-1-methyl-4-piperidinyl]-2-methyl-
[Molecular Formula]

C16H19NO5
[MDL Number]

MFCD00878456
[MOL File]

71294-60-5.mol
[Molecular Weight]

305.33
Chemical PropertiesBack Directory
[Boiling point ]

494.8±45.0 °C(Predicted)
[density ]

1.380±0.06 g/cm3(Predicted)
[pka]

6.26±0.40(Predicted)
Hazard InformationBack Directory
[Uses]

Rohitukine is an alkaloid with analgesic and anti-inflammatory activities[1].
[Definition]

ChEBI: Rohitukine is a member of the class of chromones that is 4H-chromen-4-one in which the hydrogens at positions 2,5,7 and 8 are replaced by methyl, hydroxy, hydroxy, and (3S,4R)-3-hydroxy-1-methylpiperidin-4-yl groups, respectively. It is an alkaloid initially isolated from Amoora rohituka and is a precursor of the anti-cancer compound flavopiridol. It has a role as a plant metabolite, an antineoplastic agent, an EC 2.7.11.22 (cyclin-dependent kinase) inhibitor, a fungal metabolite, an anti-inflammatory agent, an anti-ulcer drug, an anticholesteremic drug and an antileishmanial agent. It is a hydroxypiperidine, a tertiary amino compound, a member of chromones, a member of resorcinols and an alkaloid.
[References]

[1] Houghton P J, et al. Further chromone alkaloids from Schumanniophyton magnificum[J]. Planta Medica, 1987, 53(03): 262-264. DOI:10.1055/s-2006-962698
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