Suberosin
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Suberosin
structure -
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CAS No:
581-31-7
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Formula:
C15H16O3
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Chemical Name:
Suberosin
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Synonyms:
2H-1-Benzopyran-2-one,7-methoxy-6-(3-methyl-2-buten-1-yl)-;Coumarin,7-methoxy-6-(3-methyl-2-butenyl)-;Suberosin;2H-1-Benzopyran-2-one,7-methoxy-6-(3-methyl-2-butenyl)-;7-Methoxy-6-(3-methyl-2-buten-1-yl)-2H-1-benzopyran-2-one;7-Methoxy-6-(3-methyl-2-butenyl)coumarin;NSC 31869
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CAS No:
Description
Suberosin, isolated from Plumbago zeylanica, exhibits anti-inflammatory and anticoagulant activity. Suberosin suppresses PHA-induced PBMC proliferation and arrested cell cycle progression from the G1 transition to the S phase through the modulation of the transcription factors NF-AT and NF-κB[1][2].
Suberosin is a member of the class of coumarins in which the coumarin ring is substituted at positions 6 and 7 by a 3-methylbut-2-en-1-yl group and a methoxy group, respectively. A natural product found in Citropsis articulata. It has a role as a plant metabolite and an anticoagulant. It is a member of coumarins and an aromatic ether. It derives from a 7-demethylsuberosin.
Characteristics
35.5
3.87
1.1±0.1 g/cm3
87.5 °C @ Solvent: Methanol
158-172 °C @ Press: 0.05 Torr
166.0±22.5 °C
1.557
Computed Properties
Molecular Weight:244.28
XLogP3:3.8
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:244.109944368
Monoisotopic Mass:244.109944368
Topological Polar Surface Area:35.5
Heavy Atom Count:18
Complexity:366
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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