2-Methylanthracene

Details

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Internal ID 9d9410b7-89c7-4713-9cf3-5fa32606c4fb
Taxonomy Benzenoids > Anthracenes
IUPAC Name 2-methylanthracene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12/c1-11-6-7-14-9-12-4-2-3-5-13(12)10-15(14)8-11/h2-10H,1H3
InChI Key GYMFBYTZOGMSQJ-UHFFFAOYSA-N
Popularity 214 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12
Molecular Weight 192.25 g/mol
Exact Mass 192.093900383 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.30
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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613-12-7
6C868JOV4A
DTXSID8060616
NSC-87376
RefChem:475951
DTXCID6042995
210-329-3
Anthracene, 2-methyl-
MFCD00003583
26914-18-1
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-Methylanthracene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.8962 89.62%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.8258 82.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9520 95.20%
OATP1B3 inhibitior + 0.9714 97.14%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8189 81.89%
P-glycoprotein inhibitior - 0.9141 91.41%
P-glycoprotein substrate - 0.9901 99.01%
CYP3A4 substrate - 0.7554 75.54%
CYP2C9 substrate - 0.8375 83.75%
CYP2D6 substrate - 0.6845 68.45%
CYP3A4 inhibition - 0.8710 87.10%
CYP2C9 inhibition - 0.9359 93.59%
CYP2C19 inhibition - 0.9026 90.26%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition + 0.7333 73.33%
CYP2C8 inhibition - 0.8734 87.34%
CYP inhibitory promiscuity - 0.5448 54.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Warning 0.4452 44.52%
Eye corrosion + 0.6220 62.20%
Eye irritation + 0.9754 97.54%
Skin irritation + 0.8623 86.23%
Skin corrosion - 0.8430 84.30%
Ames mutagenesis + 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.6619 66.19%
Hepatotoxicity + 0.8875 88.75%
skin sensitisation + 0.9211 92.11%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7963 79.63%
Estrogen receptor binding + 0.9095 90.95%
Androgen receptor binding + 0.7853 78.53%
Thyroid receptor binding + 0.6402 64.02%
Glucocorticoid receptor binding + 0.7948 79.48%
Aromatase binding + 0.8230 82.30%
PPAR gamma + 0.5520 55.20%
Honey bee toxicity - 0.9759 97.59%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.9800 98.00%
Fish aquatic toxicity + 0.9759 97.59%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.75% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 87.34% 94.73%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.96% 94.62%
CHEMBL2581 P07339 Cathepsin D 85.97% 98.95%
CHEMBL240 Q12809 HERG 83.53% 89.76%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.34% 93.65%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.20% 91.11%
CHEMBL2039 P27338 Monoamine oxidase B 82.54% 92.51%
CHEMBL4581 P52732 Kinesin-like protein 1 81.02% 93.18%
CHEMBL221 P23219 Cyclooxygenase-1 80.49% 90.17%

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.
Pinellia ternata

Cross-Links

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PubChem 11936
NPASS NPC228476