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Lumiflavine - ≥95%, high purity , CAS No.1088-56-8

1 Citations

COA

Grade & Purity:

≥95%

Cas Number: 1088-56-8
Molecular Weight: 256.26
EC Number: 214-125-5
PubChem CID: 66184

In stock

Item Number

L338492

Grouped product items
SKU	Size	Availability	Price
L338492-25mg	25mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$228.90
L338492-50mg	50mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$410.90
L338492-100mg	100mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$593.90
L338492-250mg	250mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$1,335.90

a riboflavin uptake inhibitor used to study riboflavin uptake in intestinal epithelial (Caco-2) and other epithelial cells

Basic Description

Synonyms	7,8,10-trimethyl-2H,3H,4H,10H-benzo[g]pteridine-2,4-dione \| 7,8,10-Trimethylbenzo(g)pteridine-2,4,(3H,10H)-dione \| BENZO(G)PTERIDIN-2(10H)-ONE, 4-HYDROXY-7,8,10-TRIMETHYL- \| AKOS004910107 \| KPDQZGKJTJRBGU-UHFFFAOYSA- \| LUMIFLAVINE [MI] \| RIBOFLAVIN SODIUM
Specifications & Purity	≥95%
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Lumiflavine (Lumiflavin) is produced by the photolysis of vitamin B2 (Riboflavin). Lumiflavine, a riboflavin uptake inhibitor, is used to study riboflavin uptake in intestinal epithelial (Caco-2) and other epithelial cells

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Pteridines and derivatives
    - Subclass Alloxazines and isoalloxazines

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Pteridines and derivatives
Subclass	Alloxazines and isoalloxazines
Intermediate Tree Nodes	Not available
Direct Parent	Flavins
Alternative Parents	Quinoxalines Pyrimidones Pyrazines Benzenoids Vinylogous amides Heteroaromatic compounds Lactams Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Flavin - Diazanaphthalene - Quinoxaline - Pyrimidone - Pyrazine - Pyrimidine - Benzenoid - Heteroaromatic compound - Vinylogous amide - Lactam - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as flavins. These are compounds containing a flavin (7,8-dimethyl-benzo[g]pteridine-2,4-dione) moiety, with a structure characterized by an isoalloaxzine tricyclic ring.
External Descriptors	flavin
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	7,8,10-trimethylbenzo[g]pteridine-2,4-dione
INCHI	InChI=1S/C13H12N4O2/c1-6-4-8-9(5-7(6)2)17(3)11-10(14-8)12(18)16-13(19)15-11/h4-5H,1-3H3,(H,16,18,19)
InChIKey	KPDQZGKJTJRBGU-UHFFFAOYSA-N
Smiles	CC1=CC2=C(C=C1C)N(C3=NC(=O)NC(=O)C3=N2)C
Isomeric SMILES	CC1=CC2=C(C=C1C)N(C3=NC(=O)NC(=O)C3=N2)C
WGK Germany	3
RTECS	OK4800000
Molecular Weight	256.26
Reaxy-Rn	269756
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=269756&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

Solubility	Soluble in 20 mg/ml, 0.1 M NaOH
Molecular Weight	256.260 g/mol
XLogP3	1.100
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	0
Exact Mass	256.096 Da
Monoisotopic Mass	256.096 Da
Topological Polar Surface Area	74.100 Å²
Heavy Atom Count	19
Formal Charge	0
Complexity	511.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

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