(3-Methylpenta-1,4-diyn-3-yl)benzene

Details

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Internal ID c6f48ffb-1869-40c7-ad2c-ef7085ecaf6e
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 3-methylpenta-1,4-diyn-3-ylbenzene
SMILES (Canonical) CC(C#C)(C#C)C1=CC=CC=C1
SMILES (Isomeric) CC(C#C)(C#C)C1=CC=CC=C1
InChI InChI=1S/C12H10/c1-4-12(3,5-2)11-9-7-6-8-10-11/h1-2,6-10H,3H3
InChI Key OVVLODSLGRGWFA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H10
Molecular Weight 154.21 g/mol
Exact Mass 154.078250319 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.21
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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(3-Methylpenta-1,4-diyn-3-yl)benzene
DTXSID80758890
3-Methyl-3-phenyl-1,4-pentadiin

2D Structure

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2D Structure of (3-Methylpenta-1,4-diyn-3-yl)benzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.7703 77.03%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.5376 53.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9452 94.52%
OATP1B3 inhibitior + 0.9633 96.33%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9088 90.88%
P-glycoprotein inhibitior - 0.9785 97.85%
P-glycoprotein substrate - 0.9650 96.50%
CYP3A4 substrate - 0.7746 77.46%
CYP2C9 substrate - 0.8209 82.09%
CYP2D6 substrate - 0.7500 75.00%
CYP3A4 inhibition - 0.8261 82.61%
CYP2C9 inhibition - 0.7889 78.89%
CYP2C19 inhibition - 0.9395 93.95%
CYP2D6 inhibition - 0.9671 96.71%
CYP1A2 inhibition - 0.7290 72.90%
CYP2C8 inhibition - 0.8699 86.99%
CYP inhibitory promiscuity - 0.7587 75.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5364 53.64%
Carcinogenicity (trinary) Warning 0.4532 45.32%
Eye corrosion + 0.9661 96.61%
Eye irritation + 0.8780 87.80%
Skin irritation + 0.9091 90.91%
Skin corrosion - 0.6593 65.93%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7992 79.92%
Micronuclear - 0.9282 92.82%
Hepatotoxicity + 0.7927 79.27%
skin sensitisation + 0.9347 93.47%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.8106 81.06%
Nephrotoxicity + 0.6113 61.13%
Acute Oral Toxicity (c) III 0.8954 89.54%
Estrogen receptor binding - 0.8875 88.75%
Androgen receptor binding - 0.8441 84.41%
Thyroid receptor binding - 0.7781 77.81%
Glucocorticoid receptor binding - 0.7639 76.39%
Aromatase binding - 0.6644 66.44%
PPAR gamma - 0.8122 81.22%
Honey bee toxicity - 0.9668 96.68%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.8400 84.00%
Fish aquatic toxicity + 0.8963 89.63%

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
CHEMBL2039 P27338 Monoamine oxidase B 98.48% 92.51%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 96.20% 94.62%
CHEMBL2581 P07339 Cathepsin D 91.42% 98.95%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 88.05% 94.23%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 87.57% 94.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.17% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.00% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 83.65% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 80.32% 94.73%

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 monosperma

Cross-Links

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PubChem 71330150
LOTUS LTS0086969
wikiData Q82712561