5,5,9-Trimethyltricyclo[7.1.1.01,6]undecane-10-carbaldehyde

Details

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Internal ID 852e0399-18e5-4937-a867-122b6e4bf65c
Taxonomy Organic oxygen compounds > Organic oxides
IUPAC Name 5,5,9-trimethyltricyclo[7.1.1.01,6]undecane-10-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-13(2)6-4-7-15-10-14(3,12(15)9-16)8-5-11(13)15/h9,11-12H,4-8,10H2,1-3H3
InChI Key GDTCRHYZPCTDEY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.82
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 5,5,9-Trimethyltricyclo[7.1.1.01,6]undecane-10-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.8216 82.16%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.5193 51.93%
OATP2B1 inhibitior - 0.8484 84.84%
OATP1B1 inhibitior + 0.9252 92.52%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7716 77.16%
P-glycoprotein inhibitior - 0.9252 92.52%
P-glycoprotein substrate - 0.9435 94.35%
CYP3A4 substrate + 0.5409 54.09%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.7680 76.80%
CYP3A4 inhibition - 0.9257 92.57%
CYP2C9 inhibition - 0.7969 79.69%
CYP2C19 inhibition - 0.7984 79.84%
CYP2D6 inhibition - 0.9639 96.39%
CYP1A2 inhibition - 0.8353 83.53%
CYP2C8 inhibition - 0.8269 82.69%
CYP inhibitory promiscuity - 0.8747 87.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.5662 56.62%
Eye corrosion - 0.8780 87.80%
Eye irritation + 0.5927 59.27%
Skin irritation - 0.5659 56.59%
Skin corrosion - 0.9517 95.17%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5127 51.27%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5374 53.74%
skin sensitisation + 0.7080 70.80%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.6919 69.19%
Acute Oral Toxicity (c) III 0.6585 65.85%
Estrogen receptor binding - 0.6915 69.15%
Androgen receptor binding - 0.5229 52.29%
Thyroid receptor binding - 0.5503 55.03%
Glucocorticoid receptor binding - 0.8285 82.85%
Aromatase binding - 0.7247 72.47%
PPAR gamma - 0.7824 78.24%
Honey bee toxicity - 0.8004 80.04%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9942 99.42%

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
CHEMBL284 P27487 Dipeptidyl peptidase IV 94.45% 95.69%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.51% 97.25%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 86.81% 96.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.80% 97.09%
CHEMBL3524 P56524 Histone deacetylase 4 85.66% 92.97%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.43% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.52% 91.11%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.11% 93.04%
CHEMBL1937 Q92769 Histone deacetylase 2 82.84% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.71% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.55% 95.56%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.18% 95.50%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.17% 99.18%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 81.93% 100.00%
CHEMBL2664 P23526 Adenosylhomocysteinase 80.76% 86.67%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.38% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 72824092
LOTUS LTS0096708
wikiData Q105006951