Salfredin B aldehyde

Details

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Internal ID ca10852b-1c59-436e-97f8-e3d4a1648382
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name 7-formyl-5-hydroxy-2,2-dimethylchromene-6-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H12O5/c1-13(2)4-3-8-9(18-13)5-7(6-14)10(11(8)15)12(16)17/h3-6,15H,1-2H3,(H,16,17)
InChI Key TVKHORSYYVWKLQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12O5
Molecular Weight 248.23 g/mol
Exact Mass 248.06847348 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.09
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Salfredin B aldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9530 95.30%
Caco-2 + 0.6933 69.33%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7329 73.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7703 77.03%
OATP1B3 inhibitior + 0.9558 95.58%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8664 86.64%
P-glycoprotein inhibitior - 0.8936 89.36%
P-glycoprotein substrate - 0.8824 88.24%
CYP3A4 substrate - 0.5118 51.18%
CYP2C9 substrate - 0.8136 81.36%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.6025 60.25%
CYP2C9 inhibition + 0.7411 74.11%
CYP2C19 inhibition - 0.8073 80.73%
CYP2D6 inhibition - 0.9137 91.37%
CYP1A2 inhibition - 0.7633 76.33%
CYP2C8 inhibition - 0.7514 75.14%
CYP inhibitory promiscuity - 0.6518 65.18%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5664 56.64%
Eye corrosion - 0.9822 98.22%
Eye irritation + 0.8693 86.93%
Skin irritation - 0.5758 57.58%
Skin corrosion - 0.8586 85.86%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7249 72.49%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.5064 50.64%
skin sensitisation - 0.7250 72.50%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5749 57.49%
Acute Oral Toxicity (c) III 0.6313 63.13%
Estrogen receptor binding + 0.8900 89.00%
Androgen receptor binding - 0.5164 51.64%
Thyroid receptor binding + 0.5308 53.08%
Glucocorticoid receptor binding + 0.8718 87.18%
Aromatase binding + 0.6552 65.52%
PPAR gamma + 0.8031 80.31%
Honey bee toxicity - 0.9435 94.35%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9807 98.07%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.85% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.63% 94.45%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 95.29% 98.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.77% 95.56%
CHEMBL4208 P20618 Proteasome component C5 88.90% 90.00%
CHEMBL2581 P07339 Cathepsin D 88.53% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.09% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.67% 96.09%
CHEMBL3194 P02766 Transthyretin 86.87% 90.71%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 86.69% 94.42%
CHEMBL3401 O75469 Pregnane X receptor 84.79% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.34% 89.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139587198
LOTUS LTS0145234
wikiData Q77560279