2-(4,7-Dimethyl-1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalen-1-yl)propan-1-ol

Details

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Internal ID eb4de5cd-e61b-4e48-95ff-7c7abc1ec34b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-(4,7-dimethyl-1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalen-1-yl)propan-1-ol
SMILES (Canonical) CC1CCC2C(CCC(C2C1)C(C)CO)C
SMILES (Isomeric) CC1CCC2C(CCC(C2C1)C(C)CO)C
InChI InChI=1S/C15H28O/c1-10-4-6-13-11(2)5-7-14(12(3)9-16)15(13)8-10/h10-16H,4-9H2,1-3H3
InChI Key KGIBMKUEWBYMCC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H28O
Molecular Weight 224.38 g/mol
Exact Mass 224.214015512 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.00
Atomic LogP (AlogP) 3.71
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(4,7-Dimethyl-1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalen-1-yl)propan-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.8515 85.15%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.7379 73.79%
OATP2B1 inhibitior - 0.8457 84.57%
OATP1B1 inhibitior + 0.9370 93.70%
OATP1B3 inhibitior + 0.9050 90.50%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8869 88.69%
P-glycoprotein inhibitior - 0.9177 91.77%
P-glycoprotein substrate - 0.7660 76.60%
CYP3A4 substrate - 0.5391 53.91%
CYP2C9 substrate - 0.8218 82.18%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.8795 87.95%
CYP2C9 inhibition - 0.6676 66.76%
CYP2C19 inhibition - 0.6954 69.54%
CYP2D6 inhibition - 0.9142 91.42%
CYP1A2 inhibition - 0.5601 56.01%
CYP2C8 inhibition - 0.9035 90.35%
CYP inhibitory promiscuity - 0.7823 78.23%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.6720 67.20%
Eye corrosion - 0.7495 74.95%
Eye irritation + 0.8485 84.85%
Skin irritation - 0.7935 79.35%
Skin corrosion - 0.9333 93.33%
Ames mutagenesis - 0.7378 73.78%
Human Ether-a-go-go-Related Gene inhibition - 0.5648 56.48%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.7206 72.06%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.5757 57.57%
Acute Oral Toxicity (c) III 0.7360 73.60%
Estrogen receptor binding - 0.7414 74.14%
Androgen receptor binding + 0.5991 59.91%
Thyroid receptor binding - 0.5433 54.33%
Glucocorticoid receptor binding - 0.7279 72.79%
Aromatase binding - 0.6902 69.02%
PPAR gamma - 0.8855 88.55%
Honey bee toxicity - 0.9119 91.19%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.9603 96.03%

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 96.12% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.41% 97.25%
CHEMBL4040 P28482 MAP kinase ERK2 90.31% 83.82%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.75% 97.09%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 88.00% 97.23%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.56% 96.47%
CHEMBL2581 P07339 Cathepsin D 83.93% 98.95%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 80.76% 95.27%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.47% 93.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.35% 94.80%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 80.17% 98.46%

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.
Artemisia annua
Artemisia carvifolia

Cross-Links

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PubChem 5320412
NPASS NPC290844