Isodihydrolaurene

Details

Top
Internal ID ab4b4b9f-d3cd-45ab-9e95-9c176b7910cb
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1-[(1R,2S)-1,2-dimethyl-3-methylidenecyclopentyl]-4-methylcyclohexa-1,4-diene
SMILES (Canonical) CC1C(=C)CCC1(C)C2=CCC(=CC2)C
SMILES (Isomeric) C[C@H]1C(=C)CC[C@@]1(C)C2=CCC(=CC2)C
InChI InChI=1S/C15H22/c1-11-5-7-14(8-6-11)15(4)10-9-12(2)13(15)3/h5,8,13H,2,6-7,9-10H2,1,3-4H3/t13-,15+/m0/s1
InChI Key TWRALMCYJKWSET-DZGCQCFKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H22
Molecular Weight 202.33 g/mol
Exact Mass 202.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.65
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Isodihydrolaurene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.9327 93.27%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.6331 63.31%
OATP2B1 inhibitior - 0.8574 85.74%
OATP1B1 inhibitior + 0.9261 92.61%
OATP1B3 inhibitior - 0.2140 21.40%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.7266 72.66%
P-glycoprotein inhibitior - 0.9712 97.12%
P-glycoprotein substrate - 0.9201 92.01%
CYP3A4 substrate + 0.5818 58.18%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7640 76.40%
CYP3A4 inhibition - 0.9251 92.51%
CYP2C9 inhibition - 0.8789 87.89%
CYP2C19 inhibition - 0.8371 83.71%
CYP2D6 inhibition - 0.9548 95.48%
CYP1A2 inhibition - 0.8159 81.59%
CYP2C8 inhibition - 0.7375 73.75%
CYP inhibitory promiscuity - 0.6051 60.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Warning 0.4682 46.82%
Eye corrosion - 0.8798 87.98%
Eye irritation - 0.5972 59.72%
Skin irritation - 0.5267 52.67%
Skin corrosion - 0.9888 98.88%
Ames mutagenesis - 0.9137 91.37%
Human Ether-a-go-go-Related Gene inhibition - 0.3703 37.03%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5846 58.46%
skin sensitisation + 0.7775 77.75%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.6362 63.62%
Acute Oral Toxicity (c) III 0.8060 80.60%
Estrogen receptor binding - 0.9415 94.15%
Androgen receptor binding - 0.6483 64.83%
Thyroid receptor binding - 0.6644 66.44%
Glucocorticoid receptor binding - 0.6965 69.65%
Aromatase binding - 0.7383 73.83%
PPAR gamma - 0.7923 79.23%
Honey bee toxicity - 0.9058 90.58%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.7800 78.00%
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
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 91.84% 86.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.38% 100.00%
CHEMBL1871 P10275 Androgen Receptor 88.23% 96.43%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.22% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.00% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.84% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.76% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.70% 93.40%
CHEMBL259 P32245 Melanocortin receptor 4 82.08% 95.38%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.86% 95.89%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.23% 90.24%

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.
Eleutherococcus giraldii
Lespedeza davidii
Solanum aethiopicum
Tectona grandis

Cross-Links

Top
PubChem 14865952
NPASS NPC279870
LOTUS LTS0179192
wikiData Q105266025