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Maculosidin

CAT: 1410-M31852-01Size: 1 EachDry Ice: NoHazardous: No
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Description
Maculosidine affect the PS I electron acceptors on leaf discs, it can inhibit ATP synthesis, basal, phosphorylating and uncoupled electron transport acting as Hill reaction inhibitors on spinach chloroplasts.
CAS Number
522-19-0
Stability
≥ 2 years
Purity
>98% (HPLC)
Weight
259.3
Molecular Formula
C14H13NO4
Notes
Research use only, not for human use.
Receptor
——

Chemical Information

Maculosidine

Maculosidine is an organic heterotricyclic compound, an organonitrogen heterocyclic compound and an oxacycle.

CAS Number522-19-0
PubChem CID68222
IUPAC Name4,6,8-trimethoxyfuro[2,3-b]quinoline
Molecular FormulaC14H13NO4
Molecular Weight259.26
XLogP2.8
Topological Polar Surface Area53.7
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count5
Rotatable Bond Count3
Heavy Atom Count19
Formal Charge0
Complexity314
SMILES
COC1=CC2=C(C(=C1)OC)N=C3C(=C2OC)C=CO3
InChI
InChI=1S/C14H13NO4/c1-16-8-6-10-12(11(7-8)17-2)15-14-9(4-5-19-14)13(10)18-3/h4-7H,1-3H3
InChIKey
SHAVHFJCSQWTFF-UHFFFAOYSA-N
Chemical Structure
2D Structure
2D structure of Maculosidine
CAS: 522-19-0
CID: 68222
Formula: C14H13NO4
MW: 259.26
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight259.26
XLogP32.8
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count5
Rotatable Bond Count3
Exact Mass259.08445790
Monoisotopic Mass259.08445790
Topological Polar Surface Area53.7 Ų
Heavy Atom Count19
Formal Charge0
Complexity314
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

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