2-(3-Isopropyl-4-methyl-pent-3-en-1-ynyl)-2-methyl-cyclobutanone

Details

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Internal ID fab53f1c-90f4-4f53-95b3-164f7d553cb8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 2-methyl-2-(4-methyl-3-propan-2-ylpent-3-en-1-ynyl)cyclobutan-1-one
SMILES (Canonical) CC(C)C(=C(C)C)C#CC1(CCC1=O)C
SMILES (Isomeric) CC(C)C(=C(C)C)C#CC1(CCC1=O)C
InChI InChI=1S/C14H20O/c1-10(2)12(11(3)4)6-8-14(5)9-7-13(14)15/h10H,7,9H2,1-5H3
InChI Key RLMQWGSUQMGDGC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H20O
Molecular Weight 204.31 g/mol
Exact Mass 204.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.35
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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2-(3-Isopropyl-4-methyl-pent-3-en-1-ynyl)-2-methyl-cyclobutanone
2-(3-Isopropyl-4-methyl-3-penten-1-ynyl)-2-methylcyclobutanone #

2D Structure

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2D Structure of 2-(3-Isopropyl-4-methyl-pent-3-en-1-ynyl)-2-methyl-cyclobutanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.7902 79.02%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.4961 49.61%
OATP2B1 inhibitior - 0.8589 85.89%
OATP1B1 inhibitior + 0.9266 92.66%
OATP1B3 inhibitior + 0.8922 89.22%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.6810 68.10%
P-glycoprotein inhibitior - 0.9352 93.52%
P-glycoprotein substrate - 0.9341 93.41%
CYP3A4 substrate - 0.5240 52.40%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8310 83.10%
CYP3A4 inhibition - 0.7968 79.68%
CYP2C9 inhibition - 0.8277 82.77%
CYP2C19 inhibition - 0.6970 69.70%
CYP2D6 inhibition - 0.9103 91.03%
CYP1A2 inhibition - 0.6662 66.62%
CYP2C8 inhibition - 0.9587 95.87%
CYP inhibitory promiscuity - 0.8275 82.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.4850 48.50%
Eye corrosion - 0.8562 85.62%
Eye irritation + 0.6962 69.62%
Skin irritation + 0.7091 70.91%
Skin corrosion - 0.9125 91.25%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8111 81.11%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.7074 70.74%
skin sensitisation + 0.8589 85.89%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.8246 82.46%
Acute Oral Toxicity (c) III 0.7976 79.76%
Estrogen receptor binding - 0.7733 77.33%
Androgen receptor binding - 0.7041 70.41%
Thyroid receptor binding - 0.6665 66.65%
Glucocorticoid receptor binding - 0.6096 60.96%
Aromatase binding - 0.5648 56.48%
PPAR gamma - 0.8060 80.60%
Honey bee toxicity - 0.8596 85.96%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.8467 84.67%

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 95.17% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.26% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.41% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 87.02% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.30% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.84% 96.09%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 85.16% 85.30%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.05% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 85.00% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.20% 85.14%

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.
Atractylodes lancea
Atractylodes macrocephala

Cross-Links

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PubChem 590280
NPASS NPC128634
LOTUS LTS0227803
wikiData Q105240290