Capillinol

Details

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Internal ID 90b42e5a-311a-4b7b-8227-531de700fdfc
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 1-phenylhexa-2,4-diyn-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H10O/c1-2-3-5-10-12(13)11-8-6-4-7-9-11/h4,6-9,12-13H,1H3
InChI Key LRUCYFPADQKETK-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C12H10O
Molecular Weight 170.21 g/mol
Exact Mass 170.073164938 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.75
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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1-phenylhexa-2,4-diyn-1-ol
1574-95-4
Benzenemethanol, alpha-1,3-pentadiynyl-
1-Phenyl-2,4-hexadiyne-1-ol
LRUCYFPADQKETK-UHFFFAOYSA-
DTXSID20935663
InChI=1/C12H10O/c1-2-3-5-10-12(13)11-8-6-4-7-9-11/h4,6-9,12-13H,1H3

2D Structure

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2D Structure of Capillinol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9916 99.16%
Caco-2 + 0.7892 78.92%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6054 60.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9567 95.67%
OATP1B3 inhibitior + 0.9726 97.26%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8990 89.90%
P-glycoprotein inhibitior - 0.9791 97.91%
P-glycoprotein substrate - 0.9614 96.14%
CYP3A4 substrate - 0.7110 71.10%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.6828 68.28%
CYP3A4 inhibition - 0.9296 92.96%
CYP2C9 inhibition - 0.8982 89.82%
CYP2C19 inhibition - 0.8401 84.01%
CYP2D6 inhibition - 0.9689 96.89%
CYP1A2 inhibition - 0.5486 54.86%
CYP2C8 inhibition - 0.9708 97.08%
CYP inhibitory promiscuity - 0.8299 82.99%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) + 0.5353 53.53%
Carcinogenicity (trinary) Non-required 0.5628 56.28%
Eye corrosion + 0.9146 91.46%
Eye irritation + 0.7463 74.63%
Skin irritation + 0.9204 92.04%
Skin corrosion + 0.9141 91.41%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7601 76.01%
Micronuclear - 0.9082 90.82%
Hepatotoxicity + 0.5949 59.49%
skin sensitisation + 0.7350 73.50%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.6614 66.14%
Acute Oral Toxicity (c) II 0.7477 74.77%
Estrogen receptor binding - 0.7949 79.49%
Androgen receptor binding - 0.6637 66.37%
Thyroid receptor binding - 0.5520 55.20%
Glucocorticoid receptor binding - 0.7201 72.01%
Aromatase binding - 0.6545 65.45%
PPAR gamma - 0.6483 64.83%
Honey bee toxicity - 0.9113 91.13%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.3933 39.33%

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
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 94.50% 94.08%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 94.24% 94.62%
CHEMBL2581 P07339 Cathepsin D 93.35% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 90.31% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.96% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.11% 95.56%
CHEMBL3902 P09211 Glutathione S-transferase Pi 86.49% 93.81%
CHEMBL3401 O75469 Pregnane X receptor 82.83% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.81% 91.11%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 82.80% 94.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.77% 86.33%
CHEMBL4208 P20618 Proteasome component C5 80.10% 90.00%

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 scoparia

Cross-Links

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PubChem 5320528
LOTUS LTS0093289
wikiData Q82911736