(1S,2R)-1-(2-methylprop-1-enyl)-2-prop-1-en-2-ylcyclopropane

Details

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Internal ID 84efd8f0-f1d0-4fd8-8d31-71534f1f3d4b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name (1S,2R)-1-(2-methylprop-1-enyl)-2-prop-1-en-2-ylcyclopropane
SMILES (Canonical) CC(=CC1CC1C(=C)C)C
SMILES (Isomeric) CC(=C[C@@H]1C[C@H]1C(=C)C)C
InChI InChI=1S/C10H16/c1-7(2)5-9-6-10(9)8(3)4/h5,9-10H,3,6H2,1-2,4H3/t9-,10+/m1/s1
InChI Key DEFOFCJWKJRAGJ-ZJUUUORDSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,2R)-1-(2-methylprop-1-enyl)-2-prop-1-en-2-ylcyclopropane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.5526 55.26%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.5811 58.11%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.9566 95.66%
OATP1B3 inhibitior + 0.9124 91.24%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8870 88.70%
P-glycoprotein inhibitior - 0.9758 97.58%
P-glycoprotein substrate - 0.9275 92.75%
CYP3A4 substrate - 0.6374 63.74%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9386 93.86%
CYP2C9 inhibition - 0.8574 85.74%
CYP2C19 inhibition - 0.7446 74.46%
CYP2D6 inhibition - 0.9243 92.43%
CYP1A2 inhibition - 0.7349 73.49%
CYP2C8 inhibition - 0.9711 97.11%
CYP inhibitory promiscuity - 0.6839 68.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5483 54.83%
Carcinogenicity (trinary) Non-required 0.4496 44.96%
Eye corrosion + 0.5835 58.35%
Eye irritation + 0.9116 91.16%
Skin irritation + 0.7597 75.97%
Skin corrosion - 0.9382 93.82%
Ames mutagenesis - 0.7254 72.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6214 62.14%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8732 87.32%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7175 71.75%
Nephrotoxicity + 0.5103 51.03%
Acute Oral Toxicity (c) III 0.4817 48.17%
Estrogen receptor binding - 0.9394 93.94%
Androgen receptor binding - 0.8605 86.05%
Thyroid receptor binding - 0.8962 89.62%
Glucocorticoid receptor binding - 0.8924 89.24%
Aromatase binding - 0.8302 83.02%
PPAR gamma - 0.8582 85.82%
Honey bee toxicity - 0.6291 62.91%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9892 98.92%

Targets

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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
CHEMBL1951 P21397 Monoamine oxidase A 90.93% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.63% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.91% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 81.51% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.44% 96.95%

Plants that contains it

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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 tridentata
Castilleja integra

Cross-Links

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PubChem 13745740
LOTUS LTS0139484
wikiData Q104977153