Cardanol diene

Details

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Internal ID 5ba4227f-f468-41f2-ace8-4133f57774cf
Taxonomy Benzenoids > Phenols > 1-hydroxy-4-unsubstituted benzenoids
IUPAC Name 3-[(8Z,11Z)-pentadeca-8,11-dienyl]phenol
SMILES (Canonical) CCCC=CCC=CCCCCCCCC1=CC(=CC=C1)O
SMILES (Isomeric) CCC/C=C\C/C=C\CCCCCCCC1=CC(=CC=C1)O
InChI InChI=1S/C21H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-20-17-15-18-21(22)19-20/h4-5,7-8,15,17-19,22H,2-3,6,9-14,16H2,1H3/b5-4-,8-7-
InChI Key FAYVLNWNMNHXGA-UTOQUPLUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H32O
Molecular Weight 300.50 g/mol
Exact Mass 300.245315640 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 7.80
Atomic LogP (AlogP) 6.58
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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R5UNJ6B02F
CHEMBL470887
3-8Z,11Z-pentadecadien-1-yl-phenol
3-(8(Z),11(Z)-Pentadecadienyl)phenol
5-{8(Z),11(Z)-Pentadecadienyl}Phenol
51546-63-5
3-((8Z,11Z)-pentadeca-8,11-dien-1-yl)phenol
3-[(8Z,11Z)-Pentadeca-8,11-dien-1-yl]phenol
UNII-R5UNJ6B02F
SCHEMBL2293234
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cardanol diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 + 0.6802 68.02%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.5418 54.18%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.7095 70.95%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.7577 75.77%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.5790 57.90%
CYP3A4 substrate + 0.5195 51.95%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate + 0.3567 35.67%
CYP3A4 inhibition - 0.6465 64.65%
CYP2C9 inhibition - 0.7367 73.67%
CYP2C19 inhibition - 0.6127 61.27%
CYP2D6 inhibition - 0.8857 88.57%
CYP1A2 inhibition + 0.6748 67.48%
CYP2C8 inhibition + 0.7337 73.37%
CYP inhibitory promiscuity + 0.5892 58.92%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7011 70.11%
Carcinogenicity (trinary) Non-required 0.6004 60.04%
Eye corrosion + 0.9413 94.13%
Eye irritation - 0.6130 61.30%
Skin irritation + 0.7116 71.16%
Skin corrosion + 0.7065 70.65%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8940 89.40%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6592 65.92%
skin sensitisation + 0.9323 93.23%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.6091 60.91%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.8135 81.35%
Acute Oral Toxicity (c) III 0.8175 81.75%
Estrogen receptor binding + 0.8563 85.63%
Androgen receptor binding - 0.5945 59.45%
Thyroid receptor binding + 0.6634 66.34%
Glucocorticoid receptor binding - 0.5900 59.00%
Aromatase binding + 0.5353 53.53%
PPAR gamma + 0.8208 82.08%
Honey bee toxicity - 0.9792 97.92%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6362 63.62%
Fish aquatic toxicity + 0.9845 98.45%

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 98.82% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.04% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.30% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.27% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.75% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 90.75% 94.73%
CHEMBL240 Q12809 HERG 88.20% 89.76%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 86.19% 91.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.45% 95.56%
CHEMBL236 P41143 Delta opioid receptor 85.24% 99.35%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.74% 91.11%
CHEMBL2535 P11166 Glucose transporter 83.91% 98.75%
CHEMBL1951 P21397 Monoamine oxidase A 83.64% 91.49%
CHEMBL1781 P11387 DNA topoisomerase I 83.42% 97.00%
CHEMBL3891 P07384 Calpain 1 81.74% 93.04%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.83% 96.25%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.29% 96.95%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.03% 99.18%

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.
Anacardium occidentale
Aronia arbutifolia
Clibadium sodiroi
Discaria serratifolia
Pteris dactylina
Pyrostegia venusta
Rostellularia hayatae
Schinus terebinthifolia
Silene viscaria

Cross-Links

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PubChem 11098630
NPASS NPC210497
LOTUS LTS0203589
wikiData Q27896124