Naphthalene, 2-(2,4-hexadiynyl)-

Details

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Internal ID ec7131dc-d516-4528-b7a7-80b8c2bcd685
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 2-hexa-2,4-diynylnaphthalene
SMILES (Canonical) CC#CC#CCC1=CC2=CC=CC=C2C=C1
SMILES (Isomeric) CC#CC#CCC1=CC2=CC=CC=C2C=C1
InChI InChI=1S/C16H12/c1-2-3-4-5-8-14-11-12-15-9-6-7-10-16(15)13-14/h6-7,9-13H,8H2,1H3
InChI Key SRYARTHJKAESGC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12
Molecular Weight 204.27 g/mol
Exact Mass 204.093900383 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 3.41
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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172923-89-6
Naphthalene, 2-(2,4-hexadiynyl)-
CHEMBL448632
2-(2,4-hexadiynyl)naphthalene
DTXSID70938245
2-(HEXA-2,4-DIYN-1-YL)NAPHTHALENE

2D Structure

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2D Structure of Naphthalene, 2-(2,4-hexadiynyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.9246 92.46%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.7588 75.88%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9245 92.45%
OATP1B3 inhibitior + 0.9618 96.18%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6506 65.06%
P-glycoprotein inhibitior - 0.9708 97.08%
P-glycoprotein substrate - 0.9360 93.60%
CYP3A4 substrate - 0.6509 65.09%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3630 36.30%
CYP3A4 inhibition - 0.7219 72.19%
CYP2C9 inhibition - 0.7673 76.73%
CYP2C19 inhibition - 0.6482 64.82%
CYP2D6 inhibition - 0.9256 92.56%
CYP1A2 inhibition + 0.8560 85.60%
CYP2C8 inhibition - 0.6834 68.34%
CYP inhibitory promiscuity + 0.7476 74.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Warning 0.3715 37.15%
Eye corrosion - 0.5920 59.20%
Eye irritation + 0.9085 90.85%
Skin irritation + 0.7707 77.07%
Skin corrosion - 0.7294 72.94%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4584 45.84%
Micronuclear - 0.7661 76.61%
Hepatotoxicity + 0.6093 60.93%
skin sensitisation + 0.8852 88.52%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.6287 62.87%
Acute Oral Toxicity (c) III 0.7544 75.44%
Estrogen receptor binding + 0.6753 67.53%
Androgen receptor binding + 0.8947 89.47%
Thyroid receptor binding + 0.5170 51.70%
Glucocorticoid receptor binding - 0.6247 62.47%
Aromatase binding + 0.7942 79.42%
PPAR gamma - 0.4909 49.09%
Honey bee toxicity - 0.8647 86.47%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9821 98.21%

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
CHEMBL2581 P07339 Cathepsin D 93.02% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.52% 96.09%
CHEMBL4296013 Q5VWK5 Interleukin-23 receptor 88.25% 88.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.74% 86.33%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 85.96% 96.42%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.70% 95.50%
CHEMBL3902 P09211 Glutathione S-transferase Pi 84.62% 93.81%
CHEMBL221 P23219 Cyclooxygenase-1 82.75% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.50% 91.11%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.48% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 82.46% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.69% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.43% 99.17%
CHEMBL2535 P11166 Glucose transporter 80.63% 98.75%

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.
Santolina canescens

Cross-Links

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PubChem 177256
LOTUS LTS0045846
wikiData Q82914523