2-Furfuryl-5-methylfuran

Details

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Internal ID a1417ef4-4fc7-4cea-a286-f4dd466c55a5
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-(furan-2-ylmethyl)-5-methylfuran
SMILES (Canonical) CC1=CC=C(O1)CC2=CC=CO2
SMILES (Isomeric) CC1=CC=C(O1)CC2=CC=CO2
InChI InChI=1S/C10H10O2/c1-8-4-5-10(12-8)7-9-3-2-6-11-9/h2-6H,7H2,1H3
InChI Key LWHDEDPRANCGFI-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O2
Molecular Weight 162.18 g/mol
Exact Mass 162.068079557 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.77
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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2-Furfuryl-5-methylfuran
2-(furan-2-ylmethyl)-5-methylfuran
13678-51-8
Furan, 2-(2-furanylmethyl)-5-methyl-
5-methyl-2-furfurylfuran
SCHEMBL2266485
DTXSID50344264
LWHDEDPRANCGFI-UHFFFAOYSA-N
2-(2-Furylmethyl)-5-methylfuran
2-(2-Furanylmethyl)-5-methylfuran
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Furfuryl-5-methylfuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.7666 76.66%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.5691 56.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9109 91.09%
OATP1B3 inhibitior + 0.9596 95.96%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8897 88.97%
P-glycoprotein inhibitior - 0.9772 97.72%
P-glycoprotein substrate - 0.9390 93.90%
CYP3A4 substrate - 0.6660 66.60%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.6668 66.68%
CYP3A4 inhibition - 0.9403 94.03%
CYP2C9 inhibition - 0.8482 84.82%
CYP2C19 inhibition - 0.5457 54.57%
CYP2D6 inhibition - 0.9049 90.49%
CYP1A2 inhibition - 0.5928 59.28%
CYP2C8 inhibition - 0.8604 86.04%
CYP inhibitory promiscuity - 0.5319 53.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Danger 0.4488 44.88%
Eye corrosion + 0.4791 47.91%
Eye irritation + 0.7685 76.85%
Skin irritation + 0.6875 68.75%
Skin corrosion - 0.8075 80.75%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5784 57.84%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.5026 50.26%
skin sensitisation - 0.5456 54.56%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6135 61.35%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.4618 46.18%
Acute Oral Toxicity (c) III 0.6749 67.49%
Estrogen receptor binding - 0.7335 73.35%
Androgen receptor binding - 0.7697 76.97%
Thyroid receptor binding - 0.8094 80.94%
Glucocorticoid receptor binding - 0.4851 48.51%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.6434 64.34%
Honey bee toxicity - 0.9530 95.30%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6434 64.34%
Fish aquatic toxicity - 0.8173 81.73%

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
CHEMBL3401 O75469 Pregnane X receptor 91.95% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.54% 91.11%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.84% 93.65%
CHEMBL2581 P07339 Cathepsin D 83.72% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.92% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.20% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Azadirachta indica

Cross-Links

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PubChem 595524
LOTUS LTS0087700
wikiData Q82115989