(1E,5E,12R)-1,5,9-trimethyl-12-propan-2-ylcyclotetradeca-1,5,9-triene

Details

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Internal ID fab77454-9a78-424a-b920-9cbd7cfc8e72
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Cembrane diterpenoids
IUPAC Name (1E,5E,12R)-1,5,9-trimethyl-12-propan-2-ylcyclotetradeca-1,5,9-triene
SMILES (Canonical) CC1=CCCC(=CCC(CCC(=CCC1)C)C(C)C)C
SMILES (Isomeric) C/C/1=C\CCC(=CC[C@@H](CC/C(=C/CC1)/C)C(C)C)C
InChI InChI=1S/C20H34/c1-16(2)20-14-12-18(4)10-6-8-17(3)9-7-11-19(5)13-15-20/h8,11-12,16,20H,6-7,9-10,13-15H2,1-5H3/b17-8+,18-12?,19-11+/t20-/m0/s1
InChI Key OKMQTAYLLFRHKE-SBGUMHNNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H34
Molecular Weight 274.50 g/mol
Exact Mass 274.266051085 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.00
Atomic LogP (AlogP) 6.84
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1E,5E,12R)-1,5,9-trimethyl-12-propan-2-ylcyclotetradeca-1,5,9-triene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.9494 94.94%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Lysosomes 0.4255 42.55%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.9750 97.50%
OATP1B3 inhibitior + 0.9557 95.57%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.5297 52.97%
P-glycoprotein inhibitior - 0.7287 72.87%
P-glycoprotein substrate - 0.8967 89.67%
CYP3A4 substrate - 0.6172 61.72%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9515 95.15%
CYP2C9 inhibition - 0.8556 85.56%
CYP2C19 inhibition - 0.8447 84.47%
CYP2D6 inhibition - 0.9427 94.27%
CYP1A2 inhibition - 0.7131 71.31%
CYP2C8 inhibition - 0.9099 90.99%
CYP inhibitory promiscuity - 0.7471 74.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Warning 0.4922 49.22%
Eye corrosion + 0.5247 52.47%
Eye irritation - 0.7518 75.18%
Skin irritation + 0.7729 77.29%
Skin corrosion - 0.9586 95.86%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8262 82.62%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.9263 92.63%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.5855 58.55%
Acute Oral Toxicity (c) III 0.7428 74.28%
Estrogen receptor binding - 0.7702 77.02%
Androgen receptor binding - 0.7664 76.64%
Thyroid receptor binding + 0.5463 54.63%
Glucocorticoid receptor binding - 0.6374 63.74%
Aromatase binding - 0.7599 75.99%
PPAR gamma + 0.6170 61.70%
Honey bee toxicity - 0.9107 91.07%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9944 99.44%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.53% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.79% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.27% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.43% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.70% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.78% 93.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.33% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.89% 97.09%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 80.74% 97.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.14% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.08% 95.89%

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.
Carthamus tinctorius

Cross-Links

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PubChem 45115200
NPASS NPC72030