(5R)-5-methoxy-4,6,6-trimethylcyclohexa-1,3-diene-1-carbaldehyde

Details

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Internal ID 430dd3dd-ea1f-468c-94fa-e9bd6a30d170
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers
IUPAC Name (5R)-5-methoxy-4,6,6-trimethylcyclohexa-1,3-diene-1-carbaldehyde
SMILES (Canonical) CC1=CC=C(C(C1OC)(C)C)C=O
SMILES (Isomeric) CC1=CC=C(C([C@@H]1OC)(C)C)C=O
InChI InChI=1S/C11H16O2/c1-8-5-6-9(7-12)11(2,3)10(8)13-4/h5-7,10H,1-4H3/t10-/m1/s1
InChI Key WFMHNOKCEJZJKZ-SNVBAGLBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16O2
Molecular Weight 180.24 g/mol
Exact Mass 180.115029749 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.11
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5R)-5-methoxy-4,6,6-trimethylcyclohexa-1,3-diene-1-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.8875 88.75%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8380 83.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8459 84.59%
OATP1B3 inhibitior + 0.9661 96.61%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9433 94.33%
P-glycoprotein inhibitior - 0.9539 95.39%
P-glycoprotein substrate - 0.9411 94.11%
CYP3A4 substrate - 0.5120 51.20%
CYP2C9 substrate - 0.8063 80.63%
CYP2D6 substrate - 0.8606 86.06%
CYP3A4 inhibition - 0.8354 83.54%
CYP2C9 inhibition - 0.9209 92.09%
CYP2C19 inhibition - 0.5953 59.53%
CYP2D6 inhibition - 0.9466 94.66%
CYP1A2 inhibition - 0.7720 77.20%
CYP2C8 inhibition - 0.8540 85.40%
CYP inhibitory promiscuity - 0.5899 58.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6721 67.21%
Carcinogenicity (trinary) Non-required 0.5268 52.68%
Eye corrosion - 0.6553 65.53%
Eye irritation + 0.9490 94.90%
Skin irritation - 0.5328 53.28%
Skin corrosion - 0.9872 98.72%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5855 58.55%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.8359 83.59%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6461 64.61%
Acute Oral Toxicity (c) III 0.7996 79.96%
Estrogen receptor binding - 0.8399 83.99%
Androgen receptor binding - 0.7203 72.03%
Thyroid receptor binding - 0.8174 81.74%
Glucocorticoid receptor binding - 0.9384 93.84%
Aromatase binding - 0.7702 77.02%
PPAR gamma - 0.9022 90.22%
Honey bee toxicity - 0.6267 62.67%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.8333 83.33%

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 93.17% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.34% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.32% 94.45%

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.
Prangos tschimganica

Cross-Links

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PubChem 162847541
LOTUS LTS0186245
wikiData Q105304039