Junicedranol

Details

Top
Internal ID 9a7d2501-1394-49d1-ae16-570a6c2c8b70
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Chamigranes
IUPAC Name (1R,6R,8R)-2,2,6,7-tetramethyltricyclo[5.2.2.01,6]undecan-8-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O/c1-12(2)6-5-7-14(4)13(3)8-9-15(12,14)10-11(13)16/h11,16H,5-10H2,1-4H3/t11-,13?,14+,15-/m1/s1
InChI Key LKUBLENFVRHTGX-HYIGYNPQSA-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 4.40
Atomic LogP (AlogP) 3.75
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
SCHEMBL31571678
LKUBLENFVRHTGX-HYIGYNPQSA-N
Q67879973

2D Structure

Top
2D Structure of Junicedranol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.8271 82.71%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.4957 49.57%
OATP2B1 inhibitior - 0.8484 84.84%
OATP1B1 inhibitior + 0.9433 94.33%
OATP1B3 inhibitior + 0.9323 93.23%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9030 90.30%
P-glycoprotein inhibitior - 0.9552 95.52%
P-glycoprotein substrate - 0.9218 92.18%
CYP3A4 substrate + 0.5079 50.79%
CYP2C9 substrate - 0.7698 76.98%
CYP2D6 substrate - 0.6725 67.25%
CYP3A4 inhibition - 0.9232 92.32%
CYP2C9 inhibition - 0.7296 72.96%
CYP2C19 inhibition - 0.8298 82.98%
CYP2D6 inhibition - 0.9712 97.12%
CYP1A2 inhibition - 0.6166 61.66%
CYP2C8 inhibition - 0.9384 93.84%
CYP inhibitory promiscuity - 0.9145 91.45%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6216 62.16%
Eye corrosion - 0.9722 97.22%
Eye irritation + 0.9005 90.05%
Skin irritation + 0.7394 73.94%
Skin corrosion - 0.8860 88.60%
Ames mutagenesis - 0.6619 66.19%
Human Ether-a-go-go-Related Gene inhibition - 0.5766 57.66%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5021 50.21%
skin sensitisation + 0.5829 58.29%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.7787 77.87%
Acute Oral Toxicity (c) III 0.8025 80.25%
Estrogen receptor binding - 0.7138 71.38%
Androgen receptor binding + 0.5773 57.73%
Thyroid receptor binding - 0.7590 75.90%
Glucocorticoid receptor binding - 0.8301 83.01%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.8429 84.29%
Honey bee toxicity - 0.9303 93.03%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9570 95.70%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.76% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.78% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.63% 85.14%
CHEMBL259 P32245 Melanocortin receptor 4 86.88% 95.38%
CHEMBL1937 Q92769 Histone deacetylase 2 83.37% 94.75%
CHEMBL2039 P27338 Monoamine oxidase B 82.69% 92.51%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.22% 95.89%
CHEMBL1951 P21397 Monoamine oxidase A 80.86% 91.49%

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.
Daucus carota
Juniperus oxycedrus

Cross-Links

Top
PubChem 91753598
NPASS NPC82629
LOTUS LTS0274318
wikiData Q67879973