Capillene

Details

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Internal ID fd95e084-f9fd-4bcb-8aff-9235eb5dc8c4
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name hexa-2,4-diynylbenzene
SMILES (Canonical) CC#CC#CCC1=CC=CC=C1
SMILES (Isomeric) CC#CC#CCC1=CC=CC=C1
InChI InChI=1S/C12H10/c1-2-3-4-6-9-12-10-7-5-8-11-12/h5,7-8,10-11H,9H2,1H3
InChI Key WXQYRBLGGSLJHA-UHFFFAOYSA-N
Popularity 75 references 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 3.40
Atomic LogP (AlogP) 2.26
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Agropyrene
Benzene, 2,4-hexadiynyl-
520-74-1
Capillen
hexa-2,4-diynylbenzene
Hexa-2,4-diyn-1-ylbenzene
Capilline
2,4-Hexadiynyl-Benzene
1-Phenyl-2,4-hexadiyne
1-phenyl-hexa-2,4-diyne
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Capillene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 + 0.9428 94.28%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.9143 91.43%
Subcellular localzation Lysosomes 0.4769 47.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9385 93.85%
OATP1B3 inhibitior + 0.9630 96.30%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8797 87.97%
P-glycoprotein inhibitior - 0.9851 98.51%
P-glycoprotein substrate - 0.9409 94.09%
CYP3A4 substrate - 0.7185 71.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6862 68.62%
CYP3A4 inhibition - 0.8959 89.59%
CYP2C9 inhibition - 0.7992 79.92%
CYP2C19 inhibition - 0.8856 88.56%
CYP2D6 inhibition - 0.9592 95.92%
CYP1A2 inhibition - 0.5062 50.62%
CYP2C8 inhibition - 0.8178 81.78%
CYP inhibitory promiscuity - 0.5849 58.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6164 61.64%
Carcinogenicity (trinary) Warning 0.4460 44.60%
Eye corrosion + 0.9867 98.67%
Eye irritation + 0.8763 87.63%
Skin irritation + 0.9516 95.16%
Skin corrosion + 0.6512 65.12%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6260 62.60%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.7468 74.68%
skin sensitisation + 0.9602 96.02%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.5797 57.97%
Acute Oral Toxicity (c) III 0.8690 86.90%
Estrogen receptor binding - 0.7776 77.76%
Androgen receptor binding - 0.7069 70.69%
Thyroid receptor binding - 0.7133 71.33%
Glucocorticoid receptor binding - 0.7113 71.13%
Aromatase binding - 0.5161 51.61%
PPAR gamma - 0.7534 75.34%
Honey bee toxicity - 0.9352 93.52%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9025 90.25%

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 94.94% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 93.89% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.90% 96.09%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 89.44% 96.42%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.28% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.32% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.98% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.94% 95.50%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.90% 93.81%
CHEMBL3401 O75469 Pregnane X receptor 80.65% 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 capillaris
Artemisia dracunculus
Artemisia scoparia
Artemisia scoparia
Artemisia xanthochroa
Glebionis segetum

Cross-Links

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PubChem 3083613
NPASS NPC225221
LOTUS LTS0061561
wikiData Q27149845