(1R,4R,6S,7S)-1,4-dimethyl-7-prop-1-en-2-yl-1,2,3,4,5,6,7,8-octahydroazulen-6-ol

Details

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Internal ID 2ff0be89-f28e-46ae-a9b4-85314d25ec3b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,4R,6S,7S)-1,4-dimethyl-7-prop-1-en-2-yl-1,2,3,4,5,6,7,8-octahydroazulen-6-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-9(2)13-8-14-10(3)5-6-12(14)11(4)7-15(13)16/h10-11,13,15-16H,1,5-8H2,2-4H3/t10-,11-,13+,15+/m1/s1
InChI Key BRFKQPRYMGBIFJ-ZSEWYUTFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,4R,6S,7S)-1,4-dimethyl-7-prop-1-en-2-yl-1,2,3,4,5,6,7,8-octahydroazulen-6-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.7365 73.65%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.5755 57.55%
OATP2B1 inhibitior - 0.8482 84.82%
OATP1B1 inhibitior + 0.9401 94.01%
OATP1B3 inhibitior + 0.9089 90.89%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8896 88.96%
P-glycoprotein inhibitior - 0.8880 88.80%
P-glycoprotein substrate - 0.7479 74.79%
CYP3A4 substrate - 0.5074 50.74%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate + 0.3479 34.79%
CYP3A4 inhibition - 0.8715 87.15%
CYP2C9 inhibition - 0.8411 84.11%
CYP2C19 inhibition - 0.8537 85.37%
CYP2D6 inhibition - 0.9273 92.73%
CYP1A2 inhibition - 0.6416 64.16%
CYP2C8 inhibition - 0.8511 85.11%
CYP inhibitory promiscuity - 0.9114 91.14%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5814 58.14%
Eye corrosion - 0.9561 95.61%
Eye irritation + 0.8940 89.40%
Skin irritation + 0.5816 58.16%
Skin corrosion - 0.9334 93.34%
Ames mutagenesis - 0.7608 76.08%
Human Ether-a-go-go-Related Gene inhibition - 0.6227 62.27%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.6040 60.40%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.5937 59.37%
Acute Oral Toxicity (c) III 0.5777 57.77%
Estrogen receptor binding - 0.8082 80.82%
Androgen receptor binding - 0.6374 63.74%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.6177 61.77%
Aromatase binding - 0.8184 81.84%
PPAR gamma - 0.8065 80.65%
Honey bee toxicity - 0.8265 82.65%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9746 97.46%

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 94.98% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 92.42% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.46% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.42% 97.25%
CHEMBL2581 P07339 Cathepsin D 88.09% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.22% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 87.01% 95.93%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.77% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.17% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.26% 95.89%

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.
Cladogynos orientalis

Cross-Links

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PubChem 162937442
LOTUS LTS0196849
wikiData Q104944764