Neoisolongifolene-8-ol

Details

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Internal ID dacae826-3bd3-410c-bcb5-24cd1218fa88
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Cyclic alcohols and derivatives
IUPAC Name 5,5,11,11-tetramethyltricyclo[6.2.1.01,6]undec-6-en-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-13(2)7-6-12(16)15-8-5-10(9-11(13)15)14(15,3)4/h9-10,12,16H,5-8H2,1-4H3
InChI Key RJQXTBGTCWRVIX-UHFFFAOYSA-N
Popularity 0 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 3.40
Atomic LogP (AlogP) 3.53
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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RJQXTBGTCWRVIX-UHFFFAOYSA-N

2D Structure

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2D Structure of Neoisolongifolene-8-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8674 86.74%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.4566 45.66%
OATP2B1 inhibitior - 0.8439 84.39%
OATP1B1 inhibitior + 0.9227 92.27%
OATP1B3 inhibitior + 0.9567 95.67%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9479 94.79%
P-glycoprotein inhibitior - 0.9390 93.90%
P-glycoprotein substrate - 0.8915 89.15%
CYP3A4 substrate + 0.5104 51.04%
CYP2C9 substrate - 0.6077 60.77%
CYP2D6 substrate - 0.7196 71.96%
CYP3A4 inhibition - 0.9251 92.51%
CYP2C9 inhibition - 0.7357 73.57%
CYP2C19 inhibition - 0.6383 63.83%
CYP2D6 inhibition - 0.9332 93.32%
CYP1A2 inhibition - 0.8504 85.04%
CYP2C8 inhibition - 0.8536 85.36%
CYP inhibitory promiscuity - 0.7737 77.37%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5370 53.70%
Eye corrosion - 0.9849 98.49%
Eye irritation + 0.6438 64.38%
Skin irritation + 0.6529 65.29%
Skin corrosion - 0.9495 94.95%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4509 45.09%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6991 69.91%
skin sensitisation + 0.5999 59.99%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.7312 73.12%
Acute Oral Toxicity (c) III 0.8045 80.45%
Estrogen receptor binding - 0.7310 73.10%
Androgen receptor binding + 0.5629 56.29%
Thyroid receptor binding - 0.6150 61.50%
Glucocorticoid receptor binding - 0.7132 71.32%
Aromatase binding + 0.6491 64.91%
PPAR gamma - 0.8192 81.92%
Honey bee toxicity - 0.9136 91.36%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9787 97.87%

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
CHEMBL221 P23219 Cyclooxygenase-1 92.74% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.66% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 91.64% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.52% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.75% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.52% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.32% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.69% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.53% 94.45%

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.
Abrus melanospermus subsp. melanospermus

Cross-Links

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PubChem 596452
NPASS NPC256826