(3aR)-3,8-dimethyl-5-prop-1-en-2-yl-1,2,3,3a,4,5,6,7-octahydroazulene

Details

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Internal ID 95545463-0214-4e81-be2f-4cf4571412fa
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3aR)-3,8-dimethyl-5-prop-1-en-2-yl-1,2,3,3a,4,5,6,7-octahydroazulene
SMILES (Canonical) CC1CCC2=C(CCC(CC12)C(=C)C)C
SMILES (Isomeric) CC1CCC2=C(CCC(C[C@H]12)C(=C)C)C
InChI InChI=1S/C15H24/c1-10(2)13-7-5-11(3)14-8-6-12(4)15(14)9-13/h12-13,15H,1,5-9H2,2-4H3/t12?,13?,15-/m1/s1
InChI Key YHAJBLWYOIUHHM-SSDMNJCBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.73
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3aR)-3,8-dimethyl-5-prop-1-en-2-yl-1,2,3,3a,4,5,6,7-octahydroazulene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.9301 93.01%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.7069 70.69%
OATP2B1 inhibitior - 0.8461 84.61%
OATP1B1 inhibitior + 0.9340 93.40%
OATP1B3 inhibitior + 0.9551 95.51%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8170 81.70%
P-glycoprotein inhibitior - 0.8786 87.86%
P-glycoprotein substrate - 0.7936 79.36%
CYP3A4 substrate - 0.5171 51.71%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.6973 69.73%
CYP3A4 inhibition - 0.9414 94.14%
CYP2C9 inhibition - 0.7636 76.36%
CYP2C19 inhibition - 0.7457 74.57%
CYP2D6 inhibition - 0.9171 91.71%
CYP1A2 inhibition - 0.5965 59.65%
CYP2C8 inhibition - 0.8305 83.05%
CYP inhibitory promiscuity - 0.7944 79.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.4450 44.50%
Eye corrosion - 0.8060 80.60%
Eye irritation + 0.9439 94.39%
Skin irritation + 0.5756 57.56%
Skin corrosion - 0.9706 97.06%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4640 46.40%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.7987 79.87%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.5996 59.96%
Acute Oral Toxicity (c) III 0.8608 86.08%
Estrogen receptor binding - 0.8858 88.58%
Androgen receptor binding - 0.5232 52.32%
Thyroid receptor binding - 0.7529 75.29%
Glucocorticoid receptor binding - 0.7026 70.26%
Aromatase binding - 0.7314 73.14%
PPAR gamma - 0.8384 83.84%
Honey bee toxicity - 0.9159 91.59%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9974 99.74%

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 92.85% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.47% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 88.39% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.04% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.14% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.61% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.26% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.10% 100.00%

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.
Panax ginseng
Pogostemon cablin

Cross-Links

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PubChem 11958028
NPASS NPC200411