Lumichrome

Details

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Internal ID 0d2d7995-9e8e-4837-b138-4126562ed031
Taxonomy Organoheterocyclic compounds > Pteridines and derivatives > Alloxazines and isoalloxazines > Flavins
IUPAC Name 7,8-dimethyl-1H-benzo[g]pteridine-2,4-dione
SMILES (Canonical) CC1=CC2=C(C=C1C)N=C3C(=N2)C(=O)NC(=O)N3
SMILES (Isomeric) CC1=CC2=C(C=C1C)N=C3C(=N2)C(=O)NC(=O)N3
InChI InChI=1S/C12H10N4O2/c1-5-3-7-8(4-6(5)2)14-10-9(13-7)11(17)16-12(18)15-10/h3-4H,1-2H3,(H2,14,15,16,17,18)
InChI Key ZJTJUVIJVLLGSP-UHFFFAOYSA-N
Popularity 144 references in papers

Physical and Chemical Properties

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Molecular Formula C12H10N4O2
Molecular Weight 242.23 g/mol
Exact Mass 242.08037557 g/mol
Topological Polar Surface Area (TPSA) 84.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.78
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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7,8-Dimethylalloxazine
1086-80-2
7,8-dimethylbenzo[g]pteridine-2,4(1H,3H)-dione
Riboflavin lumichrome
Alloxazine, 7,8-dimethyl-
7,8-dimethylisoalloxazine
Benzo[g]pteridine-2,4(1H,3H)-dione, 7,8-dimethyl-
Benzo(g)pteridine-2,4(1H,3H)-dione, 7,8-dimethyl-
UNII-99U1UDJ2HM
99U1UDJ2HM
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Lumichrome

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 - 0.6250 62.50%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.7162 71.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9648 96.48%
OATP1B3 inhibitior + 0.9497 94.97%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7911 79.11%
P-glycoprotein inhibitior - 0.9459 94.59%
P-glycoprotein substrate - 0.8763 87.63%
CYP3A4 substrate - 0.6274 62.74%
CYP2C9 substrate - 0.6226 62.26%
CYP2D6 substrate - 0.8827 88.27%
CYP3A4 inhibition - 0.9560 95.60%
CYP2C9 inhibition - 0.9606 96.06%
CYP2C19 inhibition - 0.9430 94.30%
CYP2D6 inhibition - 0.9716 97.16%
CYP1A2 inhibition + 0.9136 91.36%
CYP2C8 inhibition - 0.9419 94.19%
CYP inhibitory promiscuity - 0.9750 97.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.7182 71.82%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.7012 70.12%
Skin irritation - 0.8848 88.48%
Skin corrosion - 0.9645 96.45%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6346 63.46%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.6783 67.83%
skin sensitisation - 0.9254 92.54%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.7034 70.34%
Acute Oral Toxicity (c) III 0.4983 49.83%
Estrogen receptor binding - 0.6629 66.29%
Androgen receptor binding - 0.5925 59.25%
Thyroid receptor binding - 0.5510 55.10%
Glucocorticoid receptor binding - 0.5722 57.22%
Aromatase binding + 0.6990 69.90%
PPAR gamma - 0.5558 55.58%
Honey bee toxicity - 0.9533 95.33%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.6870 68.70%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.50% 85.14%
CHEMBL230 P35354 Cyclooxygenase-2 92.81% 89.63%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.52% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 90.17% 94.73%
CHEMBL255 P29275 Adenosine A2b receptor 88.58% 98.59%
CHEMBL1937 Q92769 Histone deacetylase 2 88.41% 94.75%
CHEMBL3714130 P46095 G-protein coupled receptor 6 87.75% 97.36%
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 86.17% 95.72%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 86.06% 95.70%
CHEMBL2581 P07339 Cathepsin D 85.90% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.95% 95.56%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 84.64% 81.11%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.29% 93.03%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.95% 94.00%
CHEMBL1952 P04818 Thymidylate synthase 81.42% 93.53%
CHEMBL4302 P08183 P-glycoprotein 1 81.15% 92.98%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.03% 93.40%

Cross-Links

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PubChem 5326566
NPASS NPC282370
LOTUS LTS0108677
wikiData Q27095157