(5S)-5-hydroxy-4,6,6-trimethylcyclohexa-1,3-diene-1-carbaldehyde

Details

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Internal ID 109c579c-fb2f-45e1-8832-fcae800d2617
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name (5S)-5-hydroxy-4,6,6-trimethylcyclohexa-1,3-diene-1-carbaldehyde
SMILES (Canonical) CC1=CC=C(C(C1O)(C)C)C=O
SMILES (Isomeric) CC1=CC=C(C([C@H]1O)(C)C)C=O
InChI InChI=1S/C10H14O2/c1-7-4-5-8(6-11)10(2,3)9(7)12/h4-6,9,12H,1-3H3/t9-/m0/s1
InChI Key SCOUWBAKHRYTBW-VIFPVBQESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O2
Molecular Weight 166.22 g/mol
Exact Mass 166.099379685 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.46
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5S)-5-hydroxy-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 + 0.9965 99.65%
Caco-2 + 0.8927 89.27%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8172 81.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8590 85.90%
OATP1B3 inhibitior + 0.9664 96.64%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9192 91.92%
P-glycoprotein inhibitior - 0.9722 97.22%
P-glycoprotein substrate - 0.9591 95.91%
CYP3A4 substrate - 0.5733 57.33%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.8518 85.18%
CYP3A4 inhibition - 0.7928 79.28%
CYP2C9 inhibition - 0.8898 88.98%
CYP2C19 inhibition - 0.7947 79.47%
CYP2D6 inhibition - 0.9291 92.91%
CYP1A2 inhibition - 0.8496 84.96%
CYP2C8 inhibition - 0.9394 93.94%
CYP inhibitory promiscuity - 0.7494 74.94%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6757 67.57%
Carcinogenicity (trinary) Non-required 0.6341 63.41%
Eye corrosion - 0.5903 59.03%
Eye irritation + 0.8630 86.30%
Skin irritation + 0.7691 76.91%
Skin corrosion - 0.8247 82.47%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7695 76.95%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation + 0.9002 90.02%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.5434 54.34%
Acute Oral Toxicity (c) III 0.7991 79.91%
Estrogen receptor binding - 0.9353 93.53%
Androgen receptor binding - 0.8289 82.89%
Thyroid receptor binding - 0.8418 84.18%
Glucocorticoid receptor binding - 0.8977 89.77%
Aromatase binding - 0.8701 87.01%
PPAR gamma - 0.8940 89.40%
Honey bee toxicity - 0.8965 89.65%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.8601 86.01%

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 94.39% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.05% 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.
Dichoropetalum carvifolia

Cross-Links

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PubChem 163026356
LOTUS LTS0265913
wikiData Q105250323