Isoaromadendrene

Details

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Internal ID 9f587a70-361f-4433-8cbb-a00bd8e1de65
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Iridoids and derivatives
IUPAC Name 1,1,7-trimethyl-1a,2,4a,5,6,7,7a,7b-octahydrocyclopropa[e]azulene
SMILES (Canonical) CC1CCC2C1C3C(C3(C)C)CC=C2
SMILES (Isomeric) CC1CCC2C1C3C(C3(C)C)CC=C2
InChI InChI=1S/C14H22/c1-9-7-8-10-5-4-6-11-13(12(9)10)14(11,2)3/h4-5,9-13H,6-8H2,1-3H3
InChI Key IHQUEBHATOOKPN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22
Molecular Weight 190.32 g/mol
Exact Mass 190.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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IHQUEBHATOOKPN-UHFFFAOYSA-N
Q67879934

2D Structure

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2D Structure of Isoaromadendrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.7293 72.93%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.7667 76.67%
OATP2B1 inhibitior - 0.8553 85.53%
OATP1B1 inhibitior + 0.9116 91.16%
OATP1B3 inhibitior + 0.9531 95.31%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9738 97.38%
P-glycoprotein inhibitior - 0.9359 93.59%
P-glycoprotein substrate - 0.8458 84.58%
CYP3A4 substrate + 0.5602 56.02%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.7615 76.15%
CYP3A4 inhibition - 0.9482 94.82%
CYP2C9 inhibition - 0.8380 83.80%
CYP2C19 inhibition - 0.8173 81.73%
CYP2D6 inhibition - 0.9398 93.98%
CYP1A2 inhibition - 0.7496 74.96%
CYP2C8 inhibition - 0.7889 78.89%
CYP inhibitory promiscuity - 0.8773 87.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.5158 51.58%
Eye corrosion - 0.7804 78.04%
Eye irritation + 0.5304 53.04%
Skin irritation + 0.6617 66.17%
Skin corrosion - 0.9401 94.01%
Ames mutagenesis - 0.7953 79.53%
Human Ether-a-go-go-Related Gene inhibition + 0.6436 64.36%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.8113 81.13%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.6871 68.71%
Acute Oral Toxicity (c) III 0.6946 69.46%
Estrogen receptor binding - 0.7395 73.95%
Androgen receptor binding - 0.6351 63.51%
Thyroid receptor binding - 0.7374 73.74%
Glucocorticoid receptor binding - 0.8282 82.82%
Aromatase binding - 0.8480 84.80%
PPAR gamma - 0.8153 81.53%
Honey bee toxicity - 0.6497 64.97%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.8400 84.00%
Fish aquatic toxicity + 0.9801 98.01%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.06% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.57% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.17% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.71% 97.25%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.07% 94.80%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 86.45% 86.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.67% 96.77%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.75% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.23% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.91% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.55% 100.00%
CHEMBL1871 P10275 Androgen Receptor 80.80% 96.43%

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
Ursinia speciosa

Cross-Links

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PubChem 91752786
NPASS NPC118740
LOTUS LTS0262566
wikiData Q67879934