4-methyl-7-methylidene-2,3,4,4a,5,6,8,8a-octahydro-1H-naphthalene-1-carboxylic acid

Details

Top
Internal ID a0433923-0e62-4726-92a2-d0861ca24b79
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acids
IUPAC Name 4-methyl-7-methylidene-2,3,4,4a,5,6,8,8a-octahydro-1H-naphthalene-1-carboxylic acid
SMILES (Canonical) CC1CCC(C2C1CCC(=C)C2)C(=O)O
SMILES (Isomeric) CC1CCC(C2C1CCC(=C)C2)C(=O)O
InChI InChI=1S/C13H20O2/c1-8-3-5-10-9(2)4-6-11(13(14)15)12(10)7-8/h9-12H,1,3-7H2,2H3,(H,14,15)
InChI Key OTSWLEWDCPYCGE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C13H20O2
Molecular Weight 208.30 g/mol
Exact Mass 208.146329876 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.09
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 4-methyl-7-methylidene-2,3,4,4a,5,6,8,8a-octahydro-1H-naphthalene-1-carboxylic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.6044 60.44%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Plasma membrane 0.5719 57.19%
OATP2B1 inhibitior - 0.8442 84.42%
OATP1B1 inhibitior + 0.9490 94.90%
OATP1B3 inhibitior - 0.2214 22.14%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.5750 57.50%
BSEP inhibitior - 0.9478 94.78%
P-glycoprotein inhibitior - 0.9757 97.57%
P-glycoprotein substrate - 0.8444 84.44%
CYP3A4 substrate - 0.5433 54.33%
CYP2C9 substrate + 0.6464 64.64%
CYP2D6 substrate - 0.8657 86.57%
CYP3A4 inhibition - 0.8287 82.87%
CYP2C9 inhibition - 0.6683 66.83%
CYP2C19 inhibition - 0.6336 63.36%
CYP2D6 inhibition - 0.9289 92.89%
CYP1A2 inhibition - 0.6024 60.24%
CYP2C8 inhibition - 0.8610 86.10%
CYP inhibitory promiscuity - 0.8937 89.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5857 58.57%
Eye corrosion - 0.8236 82.36%
Eye irritation + 0.7282 72.82%
Skin irritation - 0.6376 63.76%
Skin corrosion - 0.9587 95.87%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7524 75.24%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation + 0.7738 77.38%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.5735 57.35%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7442 74.42%
Acute Oral Toxicity (c) III 0.7457 74.57%
Estrogen receptor binding - 0.7944 79.44%
Androgen receptor binding + 0.5897 58.97%
Thyroid receptor binding - 0.7137 71.37%
Glucocorticoid receptor binding - 0.5123 51.23%
Aromatase binding - 0.8579 85.79%
PPAR gamma - 0.8398 83.98%
Honey bee toxicity - 0.9375 93.75%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5100 51.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.32% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.38% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.07% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 83.24% 91.19%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.40% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.53% 93.56%

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.
Artemisia annua

Cross-Links

Top
PubChem 163061488
LOTUS LTS0005709
wikiData Q105199815