Batatasin IV

Details

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Internal ID 1479bfff-78e5-45b2-9da6-3d4e9d20a8f9
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 3-[2-(2-hydroxyphenyl)ethyl]-5-methoxyphenol
SMILES (Canonical) COC1=CC(=CC(=C1)O)CCC2=CC=CC=C2O
SMILES (Isomeric) COC1=CC(=CC(=C1)O)CCC2=CC=CC=C2O
InChI InChI=1S/C15H16O3/c1-18-14-9-11(8-13(16)10-14)6-7-12-4-2-3-5-15(12)17/h2-5,8-10,16-17H,6-7H2,1H3
InChI Key IUMFLNFLJUUODE-UHFFFAOYSA-N
Popularity 10 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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60347-67-3
3-[2-(2-hydroxyphenyl)ethyl]-5-methoxyphenol
3-[2-(2-hydroxyphenyl)ethyl]-5-methoxy-phenol
CHEBI:2997
CHEMBL228126
2',3-dihydroxy-5-methoxybibenzyl
DTXSID50209107
EX-A6737
2,3'-Dihydroxy-5'-methoxybibenzyl
BDBM50211956
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 IV

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9829 98.29%
Caco-2 + 0.8388 83.88%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.9447 94.47%
OATP2B1 inhibitior - 0.8472 84.72%
OATP1B1 inhibitior + 0.9248 92.48%
OATP1B3 inhibitior + 0.9589 95.89%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6592 65.92%
P-glycoprotein inhibitior - 0.8400 84.00%
P-glycoprotein substrate - 0.7322 73.22%
CYP3A4 substrate - 0.5444 54.44%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate + 0.5079 50.79%
CYP3A4 inhibition - 0.8606 86.06%
CYP2C9 inhibition + 0.7458 74.58%
CYP2C19 inhibition + 0.9359 93.59%
CYP2D6 inhibition - 0.8433 84.33%
CYP1A2 inhibition + 0.9034 90.34%
CYP2C8 inhibition + 0.6634 66.34%
CYP inhibitory promiscuity + 0.7596 75.96%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6854 68.54%
Carcinogenicity (trinary) Non-required 0.5755 57.55%
Eye corrosion - 0.9398 93.98%
Eye irritation + 0.9389 93.89%
Skin irritation - 0.6247 62.47%
Skin corrosion - 0.8014 80.14%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6959 69.59%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.6569 65.69%
skin sensitisation - 0.8143 81.43%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.6369 63.69%
Acute Oral Toxicity (c) III 0.6009 60.09%
Estrogen receptor binding + 0.8116 81.16%
Androgen receptor binding + 0.7761 77.61%
Thyroid receptor binding + 0.7081 70.81%
Glucocorticoid receptor binding + 0.5629 56.29%
Aromatase binding + 0.5183 51.83%
PPAR gamma + 0.6947 69.47%
Honey bee toxicity - 0.8587 85.87%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9126 91.26%

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 98.66% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.16% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.49% 96.09%
CHEMBL240 Q12809 HERG 92.18% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.76% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.54% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.42% 99.15%
CHEMBL2535 P11166 Glucose transporter 88.76% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 88.76% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.39% 93.99%
CHEMBL4208 P20618 Proteasome component C5 87.61% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.27% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.82% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.33% 92.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.55% 95.50%

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.
Alnus cordata
Aloe deltoideodonta
Bauhinia purpurea
Crinum latifolium
Dioscorea alata
Dioscorea japonica
Dioscorea oppositifolia
Dioscorea polystachya
Hemionitis aschenborniana
Leitneria floridana
Thermopsis mollis

Cross-Links

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PubChem 181271
NPASS NPC150624
LOTUS LTS0192586
wikiData Q27105920