(-)-Nopsan-4-ol

Details

Top
Internal ID 17c895d6-1f0d-46b2-90cf-ba9d2a377444
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Iridoids and derivatives
IUPAC Name (2R,6S,7R)-2,4,4,7-tetramethyltricyclo[4.3.2.01,5]undecan-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O/c1-10-5-7-15-8-6-11(10)12(15)13(2,3)9-14(15,4)16/h10-12,16H,5-9H2,1-4H3/t10-,11+,12?,14-,15?/m1/s1
InChI Key FBFJGCPGMBRKTN-WGNAFFPOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.61
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
FBFJGCPGMBRKTN-WGNAFFPOSA-N

2D Structure

Top
2D Structure of (-)-Nopsan-4-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 + 0.7397 73.97%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.6292 62.92%
OATP2B1 inhibitior - 0.8457 84.57%
OATP1B1 inhibitior + 0.9344 93.44%
OATP1B3 inhibitior + 0.9459 94.59%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9090 90.90%
P-glycoprotein inhibitior - 0.9392 93.92%
P-glycoprotein substrate - 0.9057 90.57%
CYP3A4 substrate + 0.5402 54.02%
CYP2C9 substrate + 0.6198 61.98%
CYP2D6 substrate - 0.7380 73.80%
CYP3A4 inhibition - 0.9520 95.20%
CYP2C9 inhibition - 0.6493 64.93%
CYP2C19 inhibition - 0.8164 81.64%
CYP2D6 inhibition - 0.9613 96.13%
CYP1A2 inhibition - 0.5761 57.61%
CYP2C8 inhibition - 0.8856 88.56%
CYP inhibitory promiscuity - 0.9579 95.79%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.6671 66.71%
Eye corrosion - 0.9209 92.09%
Eye irritation + 0.8479 84.79%
Skin irritation + 0.7430 74.30%
Skin corrosion - 0.8846 88.46%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5373 53.73%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6480 64.80%
skin sensitisation + 0.6576 65.76%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6586 65.86%
Acute Oral Toxicity (c) III 0.8563 85.63%
Estrogen receptor binding - 0.5331 53.31%
Androgen receptor binding + 0.7165 71.65%
Thyroid receptor binding - 0.6202 62.02%
Glucocorticoid receptor binding - 0.7042 70.42%
Aromatase binding - 0.5940 59.40%
PPAR gamma - 0.7183 71.83%
Honey bee toxicity - 0.9162 91.62%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.8642 86.42%

Targets

Top

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.49% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.06% 96.09%
CHEMBL1871 P10275 Androgen Receptor 84.92% 96.43%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.55% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.05% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.04% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.18% 92.94%

Plants that contains it

Top
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.
Echinops giganteus

Cross-Links

Top
PubChem 91748572
LOTUS LTS0036981
wikiData Q104664554