(-)-Heraclenol

Details

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Internal ID 9e29692b-bbe5-4ec5-b3f4-d3f8c1ad867b
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Furanocoumarins > Psoralens
IUPAC Name 9-[(2S)-2,3-dihydroxy-3-methylbutoxy]furo[3,2-g]chromen-7-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H16O6/c1-16(2,19)11(17)8-21-15-13-10(5-6-20-13)7-9-3-4-12(18)22-14(9)15/h3-7,11,17,19H,8H2,1-2H3/t11-/m0/s1
InChI Key FOINLJRVEBYARJ-NSHDSACASA-N
Popularity 21 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16O6
Molecular Weight 304.29 g/mol
Exact Mass 304.09468823 g/mol
Topological Polar Surface Area (TPSA) 89.10 Ų
XlogP 1.20
Atomic LogP (AlogP) 2.05
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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9-[(2S)-2,3-dihydroxy-3-methylbutoxy]furo[3,2-g]chromen-7-one
9-((2S)-2,3-dihydroxy-3-methylbutoxy)furo(3,2-g)chromen-7-one
RefChem:1049107
139079-42-8
orb1682434
FOINLJRVEBYARJ-NSHDSACASA-N
HY-N0944
AKOS040761830
FS-6892
DA-48559
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (-)-Heraclenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9667 96.67%
Caco-2 - 0.6355 63.55%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7881 78.81%
OATP2B1 inhibitior - 0.8653 86.53%
OATP1B1 inhibitior + 0.9395 93.95%
OATP1B3 inhibitior + 0.8556 85.56%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5388 53.88%
P-glycoprotein inhibitior - 0.7188 71.88%
P-glycoprotein substrate - 0.8616 86.16%
CYP3A4 substrate - 0.5751 57.51%
CYP2C9 substrate - 0.6661 66.61%
CYP2D6 substrate - 0.8264 82.64%
CYP3A4 inhibition - 0.9059 90.59%
CYP2C9 inhibition - 0.8992 89.92%
CYP2C19 inhibition - 0.8438 84.38%
CYP2D6 inhibition - 0.8449 84.49%
CYP1A2 inhibition - 0.6818 68.18%
CYP2C8 inhibition - 0.7162 71.62%
CYP inhibitory promiscuity - 0.8875 88.75%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5492 54.92%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.8090 80.90%
Skin irritation - 0.7946 79.46%
Skin corrosion - 0.9475 94.75%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4342 43.42%
Micronuclear - 0.5167 51.67%
Hepatotoxicity + 0.7158 71.58%
skin sensitisation - 0.7918 79.18%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7748 77.48%
Acute Oral Toxicity (c) III 0.7009 70.09%
Estrogen receptor binding + 0.6769 67.69%
Androgen receptor binding + 0.8089 80.89%
Thyroid receptor binding + 0.6513 65.13%
Glucocorticoid receptor binding + 0.5918 59.18%
Aromatase binding + 0.6466 64.66%
PPAR gamma + 0.7748 77.48%
Honey bee toxicity - 0.9002 90.02%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9214 92.14%

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
CHEMBL2581 P07339 Cathepsin D 97.86% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.91% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.04% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 92.11% 94.73%
CHEMBL4040 P28482 MAP kinase ERK2 91.78% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.88% 99.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.02% 97.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.78% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.19% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.81% 97.25%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.43% 93.65%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.66% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.61% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.27% 99.23%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.24% 95.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.95% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.88% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.70% 96.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.42% 99.15%

Cross-Links

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PubChem 40429858
NPASS NPC32909
LOTUS LTS0219333
wikiData Q104251417