Capillanol

Details

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Internal ID 9b043497-528a-4f5e-be35-c77ce9c53329
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 6-phenylhex-4-yn-2-ol
SMILES (Canonical) CC(CC#CCC1=CC=CC=C1)O
SMILES (Isomeric) CC(CC#CCC1=CC=CC=C1)O
InChI InChI=1S/C12H14O/c1-11(13)7-5-6-10-12-8-3-2-4-9-12/h2-4,8-9,11,13H,7,10H2,1H3
InChI Key WWNYBNQWIHBNIE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O
Molecular Weight 174.24 g/mol
Exact Mass 174.104465066 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.00
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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6-phenylhex-4-yn-2-ol
CHEBI:81335
57576-57-5
C17783
Q27155274

2D Structure

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2D Structure of Capillanol

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 + 0.9196 91.96%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.5595 55.95%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9453 94.53%
OATP1B3 inhibitior + 0.9531 95.31%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9486 94.86%
P-glycoprotein inhibitior - 0.9896 98.96%
P-glycoprotein substrate - 0.9273 92.73%
CYP3A4 substrate - 0.7154 71.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3925 39.25%
CYP3A4 inhibition - 0.8299 82.99%
CYP2C9 inhibition - 0.8246 82.46%
CYP2C19 inhibition - 0.6872 68.72%
CYP2D6 inhibition - 0.9198 91.98%
CYP1A2 inhibition + 0.6655 66.55%
CYP2C8 inhibition - 0.9131 91.31%
CYP inhibitory promiscuity - 0.8136 81.36%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) + 0.5053 50.53%
Carcinogenicity (trinary) Non-required 0.5847 58.47%
Eye corrosion - 0.6985 69.85%
Eye irritation + 0.6831 68.31%
Skin irritation + 0.7761 77.61%
Skin corrosion - 0.5922 59.22%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6115 61.15%
Micronuclear - 0.8997 89.97%
Hepatotoxicity + 0.6640 66.40%
skin sensitisation + 0.8528 85.28%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity - 0.7319 73.19%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.7705 77.05%
Acute Oral Toxicity (c) III 0.4889 48.89%
Estrogen receptor binding - 0.7902 79.02%
Androgen receptor binding - 0.8665 86.65%
Thyroid receptor binding - 0.6863 68.63%
Glucocorticoid receptor binding - 0.7106 71.06%
Aromatase binding - 0.6533 65.33%
PPAR gamma - 0.6039 60.39%
Honey bee toxicity - 0.9588 95.88%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.7624 76.24%

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 97.28% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 95.77% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.33% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.14% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.79% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 85.20% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.64% 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
Corydalis pallida

Cross-Links

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PubChem 5315669
NPASS NPC125945
LOTUS LTS0222454
wikiData Q27155274