(+)-Curcumene ether

Details

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Internal ID 0fe1fdb6-31c5-4d06-89f3-2a3ec7eb0ef2
Taxonomy Benzenoids > Benzene and substituted derivatives > Toluenes
IUPAC Name (6R)-2,2,6-trimethyl-6-(4-methylphenyl)oxane
SMILES (Canonical) CC1=CC=C(C=C1)C2(CCCC(O2)(C)C)C
SMILES (Isomeric) CC1=CC=C(C=C1)[C@]2(CCCC(O2)(C)C)C
InChI InChI=1S/C15H22O/c1-12-6-8-13(9-7-12)15(4)11-5-10-14(2,3)16-15/h6-9H,5,10-11H2,1-4H3/t15-/m1/s1
InChI Key NKSUFXDOOSPKIX-OAHLLOKOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 4.19
H-Bond Acceptor 1
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 (+)-Curcumene ether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.9429 94.29%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.6499 64.99%
OATP2B1 inhibitior - 0.8607 86.07%
OATP1B1 inhibitior + 0.9257 92.57%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8118 81.18%
P-glycoprotein inhibitior - 0.9530 95.30%
P-glycoprotein substrate - 0.9678 96.78%
CYP3A4 substrate - 0.6067 60.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3748 37.48%
CYP3A4 inhibition - 0.8478 84.78%
CYP2C9 inhibition - 0.6791 67.91%
CYP2C19 inhibition - 0.6131 61.31%
CYP2D6 inhibition - 0.9400 94.00%
CYP1A2 inhibition - 0.7278 72.78%
CYP2C8 inhibition - 0.8874 88.74%
CYP inhibitory promiscuity - 0.7437 74.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.5656 56.56%
Eye corrosion - 0.8777 87.77%
Eye irritation - 0.4818 48.18%
Skin irritation - 0.5899 58.99%
Skin corrosion - 0.9422 94.22%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5605 56.05%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6657 66.57%
skin sensitisation - 0.6031 60.31%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.5241 52.41%
Acute Oral Toxicity (c) III 0.6643 66.43%
Estrogen receptor binding + 0.7207 72.07%
Androgen receptor binding - 0.6258 62.58%
Thyroid receptor binding - 0.5307 53.07%
Glucocorticoid receptor binding - 0.7747 77.47%
Aromatase binding + 0.6591 65.91%
PPAR gamma - 0.5884 58.84%
Honey bee toxicity - 0.9575 95.75%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 0.8233 82.33%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.30% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.32% 91.11%
CHEMBL2581 P07339 Cathepsin D 83.51% 98.95%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 80.61% 90.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.20% 96.09%

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.
Curcuma aromatica
Curcuma longa
Platycladus orientalis

Cross-Links

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PubChem 11276006
NPASS NPC55464