Khusol

Details

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Internal ID d19fb9dc-a2d0-46ac-a439-0286ffddac92
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-[(1R,4aR,8aR)-7-methyl-4-methylidene-2,3,4a,5,6,8a-hexahydro-1H-naphthalen-1-yl]propan-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-10-4-6-13-11(2)5-7-14(12(3)9-16)15(13)8-10/h8,12-16H,2,4-7,9H2,1,3H3/t12?,13-,14-,15+/m0/s1
InChI Key MYDKPYLMJFRWOU-WIGRTHMWSA-N
Popularity 12 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 3.10
Atomic LogP (AlogP) 3.55
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 Khusol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9914 99.14%
Caco-2 + 0.8697 86.97%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.7247 72.47%
OATP2B1 inhibitior - 0.8496 84.96%
OATP1B1 inhibitior + 0.8950 89.50%
OATP1B3 inhibitior + 0.9248 92.48%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9088 90.88%
P-glycoprotein inhibitior - 0.9313 93.13%
P-glycoprotein substrate - 0.8421 84.21%
CYP3A4 substrate - 0.5235 52.35%
CYP2C9 substrate - 0.7919 79.19%
CYP2D6 substrate - 0.7119 71.19%
CYP3A4 inhibition - 0.7001 70.01%
CYP2C9 inhibition - 0.7352 73.52%
CYP2C19 inhibition - 0.6546 65.46%
CYP2D6 inhibition - 0.8646 86.46%
CYP1A2 inhibition - 0.6148 61.48%
CYP2C8 inhibition - 0.8854 88.54%
CYP inhibitory promiscuity - 0.5804 58.04%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6565 65.65%
Eye corrosion - 0.8849 88.49%
Eye irritation - 0.6340 63.40%
Skin irritation - 0.7370 73.70%
Skin corrosion - 0.9568 95.68%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4440 44.40%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6162 61.62%
skin sensitisation + 0.7739 77.39%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6116 61.16%
Acute Oral Toxicity (c) III 0.7939 79.39%
Estrogen receptor binding - 0.9285 92.85%
Androgen receptor binding + 0.5529 55.29%
Thyroid receptor binding - 0.6042 60.42%
Glucocorticoid receptor binding - 0.5936 59.36%
Aromatase binding - 0.8278 82.78%
PPAR gamma - 0.8764 87.64%
Honey bee toxicity - 0.9502 95.02%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9949 99.49%

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 90.18% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.25% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.29% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.74% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.27% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.29% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.36% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.16% 95.89%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 82.20% 97.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.94% 95.56%

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.
Chrysopogon zizanioides

Cross-Links

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PubChem 12304864
LOTUS LTS0249900
wikiData Q105174814