2,3-Dimethyltricyclo(2.2.1.02,6)heptane-3-carboxaldehyde

Details

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Internal ID 8b1ac89b-f45e-446a-a4fa-10b5ca047af7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 2,3-dimethyltricyclo[2.2.1.02,6]heptane-3-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O/c1-9(5-11)6-3-7-8(4-6)10(7,9)2/h5-8H,3-4H2,1-2H3
InChI Key LALMNAMACHKPDG-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.87
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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CHEBI:195897
DTXSID101202597
Q67880105
2,3-dimethyltricyclo[2.2.1.02,6]heptane-3-carbaldehyde
2,3-Dimethyltricyclo[2.2.1.02,6]heptane-3-carboxaldehyde
59300-39-9

2D Structure

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2D Structure of 2,3-Dimethyltricyclo(2.2.1.02,6)heptane-3-carboxaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.7171 71.71%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.5773 57.73%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.9484 94.84%
OATP1B3 inhibitior + 0.9529 95.29%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9034 90.34%
P-glycoprotein inhibitior - 0.9705 97.05%
P-glycoprotein substrate - 0.9298 92.98%
CYP3A4 substrate - 0.5433 54.33%
CYP2C9 substrate - 0.7907 79.07%
CYP2D6 substrate - 0.7105 71.05%
CYP3A4 inhibition - 0.8537 85.37%
CYP2C9 inhibition - 0.8058 80.58%
CYP2C19 inhibition - 0.7592 75.92%
CYP2D6 inhibition - 0.9495 94.95%
CYP1A2 inhibition - 0.8086 80.86%
CYP2C8 inhibition - 0.9568 95.68%
CYP inhibitory promiscuity - 0.8175 81.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.5735 57.35%
Eye corrosion - 0.7910 79.10%
Eye irritation + 0.7438 74.38%
Skin irritation + 0.5149 51.49%
Skin corrosion - 0.9680 96.80%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6054 60.54%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6176 61.76%
skin sensitisation + 0.7492 74.92%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.6164 61.64%
Nephrotoxicity + 0.5885 58.85%
Acute Oral Toxicity (c) III 0.4369 43.69%
Estrogen receptor binding - 0.6380 63.80%
Androgen receptor binding - 0.5293 52.93%
Thyroid receptor binding - 0.8137 81.37%
Glucocorticoid receptor binding - 0.8481 84.81%
Aromatase binding - 0.7574 75.74%
PPAR gamma - 0.7880 78.80%
Honey bee toxicity - 0.6807 68.07%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9888 98.88%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.84% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.14% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.16% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.95% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.64% 97.09%

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.
Santalum album

Cross-Links

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PubChem 85861298
LOTUS LTS0037150
wikiData Q67880105