1,3-Bis-(2-cyclopropyl,2-methylcyclopropyl)-but-2-en-1-one

Details

Top
Internal ID f66a5e5e-3112-4700-bcde-a643a2afd55d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name (Z)-1,3-bis(2-cyclopropyl-2-methylcyclopropyl)but-2-en-1-one
SMILES (Canonical) CC(=CC(=O)C1CC1(C)C2CC2)C3CC3(C)C4CC4
SMILES (Isomeric) C/C(=C/C(=O)C1CC1(C)C2CC2)/C3CC3(C)C4CC4
InChI InChI=1S/C18H26O/c1-11(14-9-17(14,2)12-4-5-12)8-16(19)15-10-18(15,3)13-6-7-13/h8,12-15H,4-7,9-10H2,1-3H3/b11-8-
InChI Key ZUFMIVCEIDLVIU-FLIBITNWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H26O
Molecular Weight 258.40 g/mol
Exact Mass 258.198365449 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.37
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
1,3-Bis-(2-cyclopropyl,2-methylcyclopropyl)-but-2-en-1-one

2D Structure

Top
2D Structure of 1,3-Bis-(2-cyclopropyl,2-methylcyclopropyl)-but-2-en-1-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.8557 85.57%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5315 53.15%
OATP2B1 inhibitior - 0.8512 85.12%
OATP1B1 inhibitior + 0.9196 91.96%
OATP1B3 inhibitior + 0.9085 90.85%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.7233 72.33%
P-glycoprotein inhibitior - 0.7520 75.20%
P-glycoprotein substrate - 0.8790 87.90%
CYP3A4 substrate + 0.5526 55.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8750 87.50%
CYP3A4 inhibition - 0.9575 95.75%
CYP2C9 inhibition - 0.8627 86.27%
CYP2C19 inhibition - 0.8130 81.30%
CYP2D6 inhibition - 0.9551 95.51%
CYP1A2 inhibition - 0.6654 66.54%
CYP2C8 inhibition - 0.9549 95.49%
CYP inhibitory promiscuity - 0.7089 70.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.5303 53.03%
Eye corrosion - 0.8359 83.59%
Eye irritation - 0.7452 74.52%
Skin irritation + 0.5989 59.89%
Skin corrosion - 0.9807 98.07%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7384 73.84%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8031 80.31%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.6314 63.14%
Acute Oral Toxicity (c) III 0.7139 71.39%
Estrogen receptor binding + 0.7581 75.81%
Androgen receptor binding - 0.6882 68.82%
Thyroid receptor binding + 0.5710 57.10%
Glucocorticoid receptor binding - 0.4649 46.49%
Aromatase binding - 0.6641 66.41%
PPAR gamma + 0.5571 55.71%
Honey bee toxicity - 0.8664 86.64%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9823 98.23%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.58% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.91% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.01% 97.25%
CHEMBL340 P08684 Cytochrome P450 3A4 87.00% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.70% 100.00%

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.
Mentha arvensis
Mentha canadensis

Cross-Links

Top
PubChem 5362887
NPASS NPC284451