2,3,4,5,6,7,8,8abeta-Octahydro-3beta,7,8,8-tetramethyl-1H-3abeta,6beta-methanoazulen-7alpha-ol

Details

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Internal ID 58d7856d-25b1-4c2b-94d9-f599f6f4dc54
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,2R,5R,7S,8S)-2,6,6,7-tetramethyltricyclo[6.2.1.01,5]undecan-7-ol
SMILES (Canonical) CC1CCC2C13CCC(C3)C(C2(C)C)(C)O
SMILES (Isomeric) C[C@@H]1CC[C@@H]2[C@@]13CC[C@@H](C3)[C@](C2(C)C)(C)O
InChI InChI=1S/C15H26O/c1-10-5-6-12-13(2,3)14(4,16)11-7-8-15(10,12)9-11/h10-12,16H,5-9H2,1-4H3/t10-,11+,12+,14+,15-/m1/s1
InChI Key IJVXAOHQRPSJDV-FUQNVFFISA-N
Popularity 0 references 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 4.10
Atomic LogP (AlogP) 3.61
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,3,4,5,6,7,8,8abeta-Octahydro-3beta,7,8,8-tetramethyl-1H-3abeta,6beta-methanoazulen-7alpha-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.6713 67.13%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.5633 56.33%
OATP2B1 inhibitior - 0.8478 84.78%
OATP1B1 inhibitior + 0.9466 94.66%
OATP1B3 inhibitior + 0.9346 93.46%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8929 89.29%
P-glycoprotein inhibitior - 0.9485 94.85%
P-glycoprotein substrate - 0.9163 91.63%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate + 0.6165 61.65%
CYP2D6 substrate - 0.7496 74.96%
CYP3A4 inhibition - 0.8893 88.93%
CYP2C9 inhibition - 0.6703 67.03%
CYP2C19 inhibition - 0.8399 83.99%
CYP2D6 inhibition - 0.9560 95.60%
CYP1A2 inhibition - 0.5268 52.68%
CYP2C8 inhibition - 0.9085 90.85%
CYP inhibitory promiscuity - 0.9098 90.98%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6521 65.21%
Eye corrosion - 0.9088 90.88%
Eye irritation + 0.8118 81.18%
Skin irritation + 0.6842 68.42%
Skin corrosion - 0.8744 87.44%
Ames mutagenesis - 0.8637 86.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6653 66.53%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5448 54.48%
skin sensitisation + 0.6535 65.35%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6505 65.05%
Acute Oral Toxicity (c) III 0.7685 76.85%
Estrogen receptor binding - 0.6413 64.13%
Androgen receptor binding - 0.6703 67.03%
Thyroid receptor binding - 0.6307 63.07%
Glucocorticoid receptor binding - 0.7336 73.36%
Aromatase binding - 0.5887 58.87%
PPAR gamma - 0.8160 81.60%
Honey bee toxicity - 0.8558 85.58%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9767 97.67%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.01% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.73% 96.09%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 86.81% 96.38%
CHEMBL206 P03372 Estrogen receptor alpha 84.84% 97.64%
CHEMBL221 P23219 Cyclooxygenase-1 84.75% 90.17%

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.
Aquilaria malaccensis
Aquilaria sinensis
Eremophila georgei

Cross-Links

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PubChem 11117656
NPASS NPC94209
LOTUS LTS0060905
wikiData Q105114168