Isobatatasin I

Details

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Internal ID 731ca2ca-898a-4cda-a047-0831a5df4664
Taxonomy Benzenoids > Phenanthrenes and derivatives > Phenanthrols
IUPAC Name 3,5,7-trimethoxyphenanthren-2-ol
SMILES (Canonical) COC1=CC(=C2C(=C1)C=CC3=CC(=C(C=C32)OC)O)OC
SMILES (Isomeric) COC1=CC(=C2C(=C1)C=CC3=CC(=C(C=C32)OC)O)OC
InChI InChI=1S/C17H16O4/c1-19-12-6-11-5-4-10-7-14(18)15(20-2)9-13(10)17(11)16(8-12)21-3/h4-9,18H,1-3H3
InChI Key BQUYXVYTCAIRQJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O4
Molecular Weight 284.31 g/mol
Exact Mass 284.10485899 g/mol
Topological Polar Surface Area (TPSA) 47.90 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.72
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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3,5,7-trimethoxyphenanthren-2-ol
39499-84-8
C10265
AC1L9D9W
CHEBI:5983
DTXSID80331920
2-hydroxy-3,5,7-trimethoxyphenanthrene
Q27106960

2D Structure

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2D Structure of Isobatatasin I

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.9065 90.65%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7055 70.55%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.9086 90.86%
OATP1B3 inhibitior + 0.9640 96.40%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7183 71.83%
P-glycoprotein inhibitior - 0.7171 71.71%
P-glycoprotein substrate - 0.8964 89.64%
CYP3A4 substrate - 0.6091 60.91%
CYP2C9 substrate - 0.7933 79.33%
CYP2D6 substrate + 0.4916 49.16%
CYP3A4 inhibition - 0.6931 69.31%
CYP2C9 inhibition - 0.9575 95.75%
CYP2C19 inhibition - 0.6790 67.90%
CYP2D6 inhibition - 0.8844 88.44%
CYP1A2 inhibition + 0.9154 91.54%
CYP2C8 inhibition + 0.5173 51.73%
CYP inhibitory promiscuity - 0.5444 54.44%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8428 84.28%
Carcinogenicity (trinary) Non-required 0.4995 49.95%
Eye corrosion - 0.9802 98.02%
Eye irritation + 0.8586 85.86%
Skin irritation - 0.6611 66.11%
Skin corrosion - 0.9777 97.77%
Ames mutagenesis + 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4328 43.28%
Micronuclear + 0.5918 59.18%
Hepatotoxicity - 0.6677 66.77%
skin sensitisation - 0.8628 86.28%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.7446 74.46%
Acute Oral Toxicity (c) III 0.4423 44.23%
Estrogen receptor binding + 0.9363 93.63%
Androgen receptor binding + 0.6676 66.76%
Thyroid receptor binding + 0.8117 81.17%
Glucocorticoid receptor binding + 0.8291 82.91%
Aromatase binding + 0.8646 86.46%
PPAR gamma + 0.7496 74.96%
Honey bee toxicity - 0.9499 94.99%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.7251 72.51%
Fish aquatic toxicity + 0.9529 95.29%

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 96.76% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.32% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.19% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.02% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.36% 92.94%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 87.93% 89.62%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 87.40% 91.79%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.28% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.89% 86.33%
CHEMBL4208 P20618 Proteasome component C5 86.84% 90.00%
CHEMBL2535 P11166 Glucose transporter 86.75% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.73% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.02% 96.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.97% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.95% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.54% 94.45%

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.
Aquilaria sinensis
Combretum psidioides
Dioscorea communis

Cross-Links

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PubChem 442708
NPASS NPC287595
LOTUS LTS0003285
wikiData Q27106960