batatasin III

Details

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Internal ID 5a225bbc-1139-43f1-80d9-3959a8cc834b
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 3-[2-(3-hydroxyphenyl)ethyl]-5-methoxyphenol
SMILES (Canonical) COC1=CC(=CC(=C1)O)CCC2=CC(=CC=C2)O
SMILES (Isomeric) COC1=CC(=CC(=C1)O)CCC2=CC(=CC=C2)O
InChI InChI=1S/C15H16O3/c1-18-15-9-12(8-14(17)10-15)6-5-11-3-2-4-13(16)7-11/h2-4,7-10,16-17H,5-6H2,1H3
InChI Key VYQXIUVIYICVCM-UHFFFAOYSA-N
Popularity 13 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O3
Molecular Weight 244.28 g/mol
Exact Mass 244.109944368 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.89
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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56684-87-8
3-[2-(3-hydroxyphenyl)ethyl]-5-methoxyphenol
1-(3-Hydroxy-5-methoxyphenyl)-2-(3-hydroxyphenyl)ethane
3,3'-dihydroxy-5-methoxybibenzyl
BatatasinIII
Batatasin III (4)
Phenol, 3-[2-(3-hydroxyphenyl)ethyl]-5-methoxy-
CHEMBL450788
SCHEMBL11505373
DTXSID00904195
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of batatasin III

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9793 97.93%
Caco-2 + 0.8970 89.70%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.9157 91.57%
OATP2B1 inhibitior - 0.7165 71.65%
OATP1B1 inhibitior + 0.9192 91.92%
OATP1B3 inhibitior + 0.9577 95.77%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5800 58.00%
P-glycoprotein inhibitior - 0.9174 91.74%
P-glycoprotein substrate - 0.5656 56.56%
CYP3A4 substrate - 0.5466 54.66%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate + 0.5079 50.79%
CYP3A4 inhibition - 0.7365 73.65%
CYP2C9 inhibition + 0.5393 53.93%
CYP2C19 inhibition + 0.9020 90.20%
CYP2D6 inhibition - 0.8480 84.80%
CYP1A2 inhibition + 0.8417 84.17%
CYP2C8 inhibition + 0.6339 63.39%
CYP inhibitory promiscuity + 0.7614 76.14%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6754 67.54%
Carcinogenicity (trinary) Non-required 0.5496 54.96%
Eye corrosion - 0.9469 94.69%
Eye irritation + 0.9677 96.77%
Skin irritation - 0.6640 66.40%
Skin corrosion - 0.8701 87.01%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7268 72.68%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.8659 86.59%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.7431 74.31%
Acute Oral Toxicity (c) III 0.6510 65.10%
Estrogen receptor binding + 0.8120 81.20%
Androgen receptor binding + 0.6235 62.35%
Thyroid receptor binding - 0.4890 48.90%
Glucocorticoid receptor binding + 0.6263 62.63%
Aromatase binding + 0.5818 58.18%
PPAR gamma + 0.7453 74.53%
Honey bee toxicity - 0.9176 91.76%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.7770 77.70%

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
CHEMBL2581 P07339 Cathepsin D 96.98% 98.95%
CHEMBL240 Q12809 HERG 96.18% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.94% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.44% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.05% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 91.01% 94.73%
CHEMBL2535 P11166 Glucose transporter 89.94% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.60% 99.17%
CHEMBL3231 Q13464 Rho-associated protein kinase 1 88.13% 95.55%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.71% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.15% 99.15%
CHEMBL1907 P15144 Aminopeptidase N 85.11% 93.31%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.92% 94.00%
CHEMBL4208 P20618 Proteasome component C5 83.06% 90.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.74% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.30% 95.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.18% 95.89%

Cross-Links

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PubChem 10466989
NPASS NPC22610
ChEMBL CHEMBL450788
LOTUS LTS0113917
wikiData Q82873435