(+)-Thalicarpine
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(+)-Thalicarpine
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CAS No:
5373-42-2
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Formula:
C41H48N2O8
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Chemical Name:
(+)-Thalicarpine
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Synonyms:
4H-Dibenzo[de,g]quinoline,9-[4,5-dimethoxy-2-[[(1S)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolinyl]methyl]phenoxy]-5,6,6a,7-tetrahydro-1,2,10-trimethoxy-6-methyl-,(6aS)-;6aα-Aporphine,9-[[4,5-dimethoxy-α-((S)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolyl)-o-tolyl]oxy]-1,2,10-trimethoxy-;Thalicarpine;4H-Dibenzo[de,g]quinoline,9-[4,5-dimethoxy-2-[(1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolinyl)methyl]phenoxy]-5,6,6a,7-tetrahydro-1,2,10-trimethoxy-6-methyl-,[S-(R*,R*)]-;(6aS)-9-[4,5-Dimethoxy-2-[[(1S)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolinyl]methyl]phenoxy]-5,6,6a,7-tetrahydro-1,2,10-trimethoxy-6-methyl-4H-dibenzo[de,g]quinoline;Thaliblastine;Thalicarpin;(+)-Thalicarpine;Taliblastine;NSC 68075
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CAS No:
Description
Thalicarpine is a member of isoquinolines and a bisbenzylisoquinoline alkaloid.|Thalicarpine is a natural aporphine benzylisoquinoline vinca alkaloid with antineoplastic activity. Thalicarpine binds to and inhibits p-glycoprotein, the multidrug resistance efflux pump. Thalicarpine also induces single-strand breaks in DNA and arrests cancer cells at the G2/M and G1 phase of the cell cycle. (NCI04)
Computed Properties
Molecular Weight:696.8
XLogP3:6.7
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:11
Exact Mass:696.34106649
Monoisotopic Mass:696.34106649
Topological Polar Surface Area:80.3
Heavy Atom Count:51
Complexity:1120
Defined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes