Naviculol

Details

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Internal ID 2c4c18f8-4f45-40bb-a374-68c2d411224d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2E)-2-[(1R,3aS,4R,7aS)-1,3a,4,7a-tetramethyl-1,2,3,4,6,7-hexahydroinden-5-ylidene]ethanol
SMILES (Canonical) CC1CCC2(C1(CCC(=CCO)C2C)C)C
SMILES (Isomeric) C[C@@H]1CC[C@@]2([C@]1(CC/C(=C\CO)/[C@H]2C)C)C
InChI InChI=1S/C15H26O/c1-11-5-8-15(4)12(2)13(7-10-16)6-9-14(11,15)3/h7,11-12,16H,5-6,8-10H2,1-4H3/b13-7+/t11-,12-,14+,15+/m1/s1
InChI Key RMIRDGFNJKHARM-LAPNCVBBSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.78
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL504928

2D Structure

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2D Structure of Naviculol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9916 99.16%
Caco-2 + 0.8329 83.29%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.8412 84.12%
OATP2B1 inhibitior - 0.8471 84.71%
OATP1B1 inhibitior + 0.8846 88.46%
OATP1B3 inhibitior + 0.8628 86.28%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8528 85.28%
P-glycoprotein inhibitior - 0.9213 92.13%
P-glycoprotein substrate - 0.9147 91.47%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.7500 75.00%
CYP2C9 inhibition - 0.7497 74.97%
CYP2C19 inhibition - 0.7736 77.36%
CYP2D6 inhibition - 0.9122 91.22%
CYP1A2 inhibition - 0.7822 78.22%
CYP2C8 inhibition - 0.7759 77.59%
CYP inhibitory promiscuity - 0.5749 57.49%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6013 60.13%
Eye corrosion - 0.9574 95.74%
Eye irritation - 0.6609 66.09%
Skin irritation - 0.5799 57.99%
Skin corrosion - 0.9737 97.37%
Ames mutagenesis - 0.8170 81.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4765 47.65%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5817 58.17%
skin sensitisation + 0.6023 60.23%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.7301 73.01%
Acute Oral Toxicity (c) III 0.8041 80.41%
Estrogen receptor binding - 0.8025 80.25%
Androgen receptor binding + 0.5198 51.98%
Thyroid receptor binding - 0.6241 62.41%
Glucocorticoid receptor binding - 0.7559 75.59%
Aromatase binding - 0.6955 69.55%
PPAR gamma - 0.7862 78.62%
Honey bee toxicity - 0.9061 90.61%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9870 98.70%

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 94.14% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.96% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.34% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.01% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.29% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.71% 97.09%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.04% 95.50%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 82.82% 83.57%
CHEMBL206 P03372 Estrogen receptor alpha 81.40% 97.64%
CHEMBL1937 Q92769 Histone deacetylase 2 81.03% 94.75%
CHEMBL1977 P11473 Vitamin D receptor 80.95% 99.43%

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.
Frullanoides densifolia
Porella navicularis

Cross-Links

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PubChem 14313693
LOTUS LTS0274875
wikiData Q104402167