(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalene-1-carbaldehyde

Details

Top
Internal ID 6fd632a0-0e66-4a63-9cdf-08671d8e78c0
Taxonomy Organic oxygen compounds > Organic oxides
IUPAC Name (1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalene-1-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-11-6-7-13-14(2,3)8-5-9-15(13,4)12(11)10-16/h10,12-13H,1,5-9H2,2-4H3/t12-,13-,15+/m1/s1
InChI Key CYNSNODFYUHSCP-NFAWXSAZSA-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 4.20
Atomic LogP (AlogP) 3.98
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalene-1-carbaldehyde

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.7213 72.13%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.5054 50.54%
OATP2B1 inhibitior - 0.8520 85.20%
OATP1B1 inhibitior + 0.8545 85.45%
OATP1B3 inhibitior - 0.3313 33.13%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8814 88.14%
P-glycoprotein inhibitior - 0.9304 93.04%
P-glycoprotein substrate - 0.9546 95.46%
CYP3A4 substrate + 0.5487 54.87%
CYP2C9 substrate - 0.6147 61.47%
CYP2D6 substrate - 0.7806 78.06%
CYP3A4 inhibition - 0.8446 84.46%
CYP2C9 inhibition - 0.6895 68.95%
CYP2C19 inhibition + 0.5277 52.77%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition - 0.7971 79.71%
CYP2C8 inhibition - 0.7898 78.98%
CYP inhibitory promiscuity - 0.6123 61.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.5647 56.47%
Eye corrosion - 0.9614 96.14%
Eye irritation - 0.5613 56.13%
Skin irritation - 0.5602 56.02%
Skin corrosion - 0.9767 97.67%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4120 41.20%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5406 54.06%
skin sensitisation + 0.8399 83.99%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.5235 52.35%
Acute Oral Toxicity (c) III 0.7778 77.78%
Estrogen receptor binding - 0.6560 65.60%
Androgen receptor binding - 0.6026 60.26%
Thyroid receptor binding - 0.6056 60.56%
Glucocorticoid receptor binding - 0.7849 78.49%
Aromatase binding - 0.7120 71.20%
PPAR gamma - 0.7571 75.71%
Honey bee toxicity - 0.8949 89.49%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 1.0000 100.00%

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 94.95% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.55% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.78% 100.00%
CHEMBL1871 P10275 Androgen Receptor 88.36% 96.43%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.35% 95.56%
CHEMBL1977 P11473 Vitamin D receptor 86.29% 99.43%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.95% 97.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.30% 99.18%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 82.18% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.09% 95.50%

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.
Diplophyllum serrulatum

Cross-Links

Top
PubChem 11298980
LOTUS LTS0141399
wikiData Q104972435