Cypera-2,4(15)-diene

Details

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Internal ID e428b7fa-0a9a-4796-b7e3-bb6b307e837a
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 10,11,11-trimethyl-4-methylidenetricyclo[5.3.1.01,5]undec-2-ene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22/c1-10-7-8-15-11(2)5-6-12(9-13(10)15)14(15,3)4/h7-8,11-13H,1,5-6,9H2,2-4H3
InChI Key KZABVHBACHSSNR-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H22
Molecular Weight 202.33 g/mol
Exact Mass 202.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.19
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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(3aR,4R,7R,8aS)-4,9,9-Trimethyl-1-methylene-4,5,6,7,8,8a-hexahydro-1H-3a,7-methanoazulene
1H-3a,7-Methanoazulene, 4,5,6,7,8,8a-hexahydro-4,9,9-trimethyl-1-methylene-, (3aR,4R,7R,8aS)-
RefChem:130136
KZABVHBACHSSNR-UHFFFAOYSA-N

2D Structure

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2D Structure of Cypera-2,4(15)-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.8407 84.07%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Lysosomes 0.7618 76.18%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9186 91.86%
OATP1B3 inhibitior + 0.9100 91.00%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9452 94.52%
P-glycoprotein inhibitior - 0.9445 94.45%
P-glycoprotein substrate - 0.6959 69.59%
CYP3A4 substrate + 0.5699 56.99%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.7897 78.97%
CYP3A4 inhibition - 0.8805 88.05%
CYP2C9 inhibition - 0.7311 73.11%
CYP2C19 inhibition - 0.7087 70.87%
CYP2D6 inhibition - 0.9271 92.71%
CYP1A2 inhibition - 0.7613 76.13%
CYP2C8 inhibition - 0.9134 91.34%
CYP inhibitory promiscuity - 0.7510 75.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.4694 46.94%
Eye corrosion - 0.9159 91.59%
Eye irritation - 0.4870 48.70%
Skin irritation + 0.5764 57.64%
Skin corrosion - 0.9774 97.74%
Ames mutagenesis - 0.9015 90.15%
Human Ether-a-go-go-Related Gene inhibition - 0.4645 46.45%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation + 0.8240 82.40%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6119 61.19%
Acute Oral Toxicity (c) III 0.8424 84.24%
Estrogen receptor binding - 0.7014 70.14%
Androgen receptor binding - 0.5164 51.64%
Thyroid receptor binding - 0.7396 73.96%
Glucocorticoid receptor binding - 0.8083 80.83%
Aromatase binding - 0.7464 74.64%
PPAR gamma - 0.7735 77.35%
Honey bee toxicity - 0.8466 84.66%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.07% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.58% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.47% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.14% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.58% 100.00%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.35% 86.00%
CHEMBL2996 Q05655 Protein kinase C delta 82.12% 97.79%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 81.82% 83.57%

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.
Cyperus rotundus

Cross-Links

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PubChem 91710045
NPASS NPC238739
LOTUS LTS0220435
wikiData Q105148022