Basic information Safety Supplier Related

norisoboldine

Basic information Safety Supplier Related

norisoboldine Basic information

Product Name:
norisoboldine
Synonyms:
  • norisoboldine
  • (+)-Laurelliptine
  • (+)-N-Norisoboldine
  • (6aS)-5,6,6a,7-Tetrahydro-2,10-dimethoxy-4H-dibenzo[de,g]quinoline-1,9-diol
  • (S)-(+)-Laurelliptine
  • Norisoboldine, 98%, from Lindera aggregata (Sims) Kosterm.
  • 4H-Dibenzo[de,g]quinoline-1,9-diol, 5,6,6a,7-tetrahydro-2,10-dimethoxy-, (6aS)-
  • (+)-Norisoboldine
CAS:
23599-69-1
MF:
C18H19NO4
MW:
313.35
Product Categories:
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
Mol File:
23599-69-1.mol
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norisoboldine Chemical Properties

Melting point:
89-191℃
Boiling point:
553.0±50.0 °C(Predicted)
Density 
1.313
solubility 
≥ 31.3mg/mL in DMSO
pka
9.58±0.20(Predicted)
form 
Powder
color 
Brown to khaki
InChI
InChI=1S/C18H19NO4/c1-22-14-8-11-10(6-13(14)20)5-12-16-9(3-4-19-12)7-15(23-2)18(21)17(11)16/h6-8,12,19-21H,3-5H2,1-2H3/t12-/m0/s1
InChIKey
HORZNQYQXBFWNZ-LBPRGKRZSA-N
SMILES
N1[C@]2([H])C3=C(C(O)=C(OC)C=C3CC1)C1=CC(OC)=C(O)C=C1C2
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Safety Information

Safety Statements 
24/25
HS Code 
29339900
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norisoboldine Usage And Synthesis

Chemical Properties

Brown crystalline powder, soluble in methanol, derived from Linderae odorata.

Uses

(+)-Norisoboldine is an anti-arthritis alkaloid isolated from radix linderae which has been shown to attenuate osteoclast differentiation and inflammatory bone erosion in aryl hydrocarbon receptor-dependant manner.

in vivo

Norisoboldine (10~40 mg/kg; p.o.; 20 days) significantly reduces the severity of joint swelling and erythema during the course of the experiment[1].
Norisoboldine (40 mg/kg; i.g.; 10 days) induces enhancement of CYP1A1 expression and suppresses expressions of Glut1 and HK2 in colons[2].

Animal Model:Male ICR mice (18–22 g)
Dosage:10~40 mg/kg
Administration:P.o.
Result:Significantly reduced the severity of joint swelling and erythema during the course of the experiment.
Animal Model:Female C57BL/6 mice (18–22 g)
Dosage:40 mg/kg
Administration:I.g.
Result:Induced enhancement of CYP1A1 expression and suppressed expressions of Glut1 and HK2 in colons.

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