1-(2-Methoxyphenyl)-2,4-hexadiyne

Details

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Internal ID 29933ea0-dc13-4299-bffe-17bee635f507
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name 1-hexa-2,4-diynyl-2-methoxybenzene
SMILES (Canonical) CC#CC#CCC1=CC=CC=C1OC
SMILES (Isomeric) CC#CC#CCC1=CC=CC=C1OC
InChI InChI=1S/C13H12O/c1-3-4-5-6-9-12-10-7-8-11-13(12)14-2/h7-8,10-11H,9H2,1-2H3
InChI Key AWBXMNYCXOZEMM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12O
Molecular Weight 184.23 g/mol
Exact Mass 184.088815002 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 2.26
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(2-Methoxyphenyl)-2,4-hexadiyne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9090 90.90%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8022 80.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9423 94.23%
OATP1B3 inhibitior + 0.9642 96.42%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9405 94.05%
P-glycoprotein inhibitior - 0.9852 98.52%
P-glycoprotein substrate - 0.8321 83.21%
CYP3A4 substrate - 0.5834 58.34%
CYP2C9 substrate - 0.7865 78.65%
CYP2D6 substrate + 0.3979 39.79%
CYP3A4 inhibition - 0.8831 88.31%
CYP2C9 inhibition - 0.9147 91.47%
CYP2C19 inhibition - 0.5770 57.70%
CYP2D6 inhibition - 0.8852 88.52%
CYP1A2 inhibition + 0.7523 75.23%
CYP2C8 inhibition - 0.6882 68.82%
CYP inhibitory promiscuity + 0.6884 68.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.5028 50.28%
Eye corrosion + 0.8777 87.77%
Eye irritation + 0.5393 53.93%
Skin irritation + 0.5270 52.70%
Skin corrosion + 0.5138 51.38%
Ames mutagenesis - 0.6054 60.54%
Human Ether-a-go-go-Related Gene inhibition - 0.3748 37.48%
Micronuclear - 0.9082 90.82%
Hepatotoxicity + 0.6895 68.95%
skin sensitisation + 0.8331 83.31%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6341 63.41%
Acute Oral Toxicity (c) III 0.8707 87.07%
Estrogen receptor binding - 0.6882 68.82%
Androgen receptor binding - 0.7441 74.41%
Thyroid receptor binding - 0.6593 65.93%
Glucocorticoid receptor binding - 0.6721 67.21%
Aromatase binding - 0.5090 50.90%
PPAR gamma - 0.8031 80.31%
Honey bee toxicity - 0.8525 85.25%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.8831 88.31%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.54% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.10% 86.33%
CHEMBL2581 P07339 Cathepsin D 88.91% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.38% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.24% 95.56%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.49% 89.62%
CHEMBL1255126 O15151 Protein Mdm4 86.27% 90.20%
CHEMBL2535 P11166 Glucose transporter 85.67% 98.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.39% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.52% 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.
Artemisia capillaris
Camptotheca acuminata

Cross-Links

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PubChem 5319414
NPASS NPC150050
LOTUS LTS0217057
wikiData Q104919941