2-(3,8,8-Trimethyl-1,2,5,6,7,8a-hexahydronaphthalen-4a-yl)acetaldehyde

Details

Top
Internal ID fde42949-846b-468e-a9c2-dc87709c943b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 2-(3,8,8-trimethyl-1,2,5,6,7,8a-hexahydronaphthalen-4a-yl)acetaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-12-5-6-13-14(2,3)7-4-8-15(13,11-12)9-10-16/h10-11,13H,4-9H2,1-3H3
InChI Key KBOSOCFVHDLFBV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.13
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-(3,8,8-Trimethyl-1,2,5,6,7,8a-hexahydronaphthalen-4a-yl)acetaldehyde

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.8994 89.94%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.3387 33.87%
OATP2B1 inhibitior - 0.8500 85.00%
OATP1B1 inhibitior + 0.8809 88.09%
OATP1B3 inhibitior + 0.9066 90.66%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7165 71.65%
P-glycoprotein inhibitior - 0.9601 96.01%
P-glycoprotein substrate - 0.8944 89.44%
CYP3A4 substrate + 0.5517 55.17%
CYP2C9 substrate - 0.6147 61.47%
CYP2D6 substrate - 0.7806 78.06%
CYP3A4 inhibition - 0.8565 85.65%
CYP2C9 inhibition - 0.7681 76.81%
CYP2C19 inhibition - 0.6320 63.20%
CYP2D6 inhibition - 0.9493 94.93%
CYP1A2 inhibition - 0.7957 79.57%
CYP2C8 inhibition - 0.7256 72.56%
CYP inhibitory promiscuity - 0.6269 62.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.5742 57.42%
Eye corrosion - 0.9398 93.98%
Eye irritation + 0.7712 77.12%
Skin irritation - 0.5161 51.61%
Skin corrosion - 0.9688 96.88%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6920 69.20%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5077 50.77%
skin sensitisation + 0.8830 88.30%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6391 63.91%
Acute Oral Toxicity (c) III 0.8192 81.92%
Estrogen receptor binding - 0.8616 86.16%
Androgen receptor binding - 0.7205 72.05%
Thyroid receptor binding - 0.6280 62.80%
Glucocorticoid receptor binding - 0.8172 81.72%
Aromatase binding - 0.7782 77.82%
PPAR gamma - 0.7835 78.35%
Honey bee toxicity - 0.9334 93.34%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9932 99.32%

Targets

Top

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.49% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.14% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.94% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.04% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.41% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.07% 97.09%
CHEMBL2581 P07339 Cathepsin D 84.75% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.96% 93.40%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.52% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 80.13% 94.73%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 14682278
LOTUS LTS0190977
wikiData Q105138404