2-Carene-8-acetamide

Details

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Internal ID 434cf677-2464-4a54-9d17-8060cf567ce6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name N-[[(1R,6S,7R)-3,7-dimethyl-7-bicyclo[4.1.0]hept-2-enyl]methyl]acetamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H19NO/c1-8-4-5-10-11(6-8)12(10,3)7-13-9(2)14/h6,10-11H,4-5,7H2,1-3H3,(H,13,14)/t10-,11+,12+/m0/s1
InChI Key JAGDLCPTTCENAK-QJPTWQEYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H19NO
Molecular Weight 193.28 g/mol
Exact Mass 193.146664230 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.11
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Carene-8-acetamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9849 98.49%
Caco-2 + 0.6088 60.88%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.5911 59.11%
OATP2B1 inhibitior - 0.8496 84.96%
OATP1B1 inhibitior + 0.9051 90.51%
OATP1B3 inhibitior + 0.9330 93.30%
MATE1 inhibitior - 0.8886 88.86%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.9729 97.29%
P-glycoprotein inhibitior - 0.9479 94.79%
P-glycoprotein substrate - 0.7903 79.03%
CYP3A4 substrate + 0.5676 56.76%
CYP2C9 substrate - 0.5888 58.88%
CYP2D6 substrate - 0.8443 84.43%
CYP3A4 inhibition - 0.7984 79.84%
CYP2C9 inhibition - 0.6628 66.28%
CYP2C19 inhibition - 0.6229 62.29%
CYP2D6 inhibition - 0.8629 86.29%
CYP1A2 inhibition - 0.5813 58.13%
CYP2C8 inhibition - 0.8849 88.49%
CYP inhibitory promiscuity - 0.5566 55.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.5752 57.52%
Eye corrosion - 0.9548 95.48%
Eye irritation - 0.9311 93.11%
Skin irritation - 0.7095 70.95%
Skin corrosion - 0.9338 93.38%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5574 55.74%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.5801 58.01%
skin sensitisation - 0.7125 71.25%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.5833 58.33%
Acute Oral Toxicity (c) III 0.6904 69.04%
Estrogen receptor binding - 0.8430 84.30%
Androgen receptor binding - 0.6311 63.11%
Thyroid receptor binding - 0.7577 75.77%
Glucocorticoid receptor binding - 0.7168 71.68%
Aromatase binding - 0.7816 78.16%
PPAR gamma - 0.7934 79.34%
Honey bee toxicity - 0.9386 93.86%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9521 95.21%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.79% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.16% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 95.02% 83.82%
CHEMBL2581 P07339 Cathepsin D 86.49% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.33% 97.25%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.95% 94.33%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.99% 100.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.58% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.30% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.59% 94.45%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139591326
LOTUS LTS0270702
wikiData Q105123753