Allohedycariol

Details

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Internal ID 6e263a60-0743-43f5-a61c-e96e29e684c0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name (1E)-10-methyl-6-methylidene-3-propan-2-ylcyclodecene
SMILES (Canonical) CC1CCCC(=C)CCC(C=C1)C(C)C
SMILES (Isomeric) CC\1CCCC(=C)CCC(/C=C1)C(C)C
InChI InChI=1S/C15H26/c1-12(2)15-10-8-13(3)6-5-7-14(4)9-11-15/h9,11-12,14-15H,3,5-8,10H2,1-2,4H3/b11-9+
InChI Key ZWZJYKZYTGYQBZ-PKNBQFBNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26
Molecular Weight 206.37 g/mol
Exact Mass 206.203450829 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.97
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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SCHEMBL30648083
ZWZJYKZYTGYQBZ-PKNBQFBNSA-N

2D Structure

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2D Structure of Allohedycariol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.9192 91.92%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.4651 46.51%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.9248 92.48%
OATP1B3 inhibitior + 0.9412 94.12%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8544 85.44%
P-glycoprotein inhibitior - 0.9536 95.36%
P-glycoprotein substrate - 0.8533 85.33%
CYP3A4 substrate - 0.6437 64.37%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.7561 75.61%
CYP3A4 inhibition - 0.9422 94.22%
CYP2C9 inhibition - 0.8228 82.28%
CYP2C19 inhibition - 0.7961 79.61%
CYP2D6 inhibition - 0.9409 94.09%
CYP1A2 inhibition - 0.6853 68.53%
CYP2C8 inhibition - 0.9381 93.81%
CYP inhibitory promiscuity - 0.7758 77.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Warning 0.5024 50.24%
Eye corrosion + 0.5274 52.74%
Eye irritation + 0.7824 78.24%
Skin irritation + 0.7425 74.25%
Skin corrosion - 0.9779 97.79%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7122 71.22%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7410 74.10%
skin sensitisation + 0.8987 89.87%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.8527 85.27%
Acute Oral Toxicity (c) III 0.8141 81.41%
Estrogen receptor binding - 0.9039 90.39%
Androgen receptor binding - 0.8765 87.65%
Thyroid receptor binding - 0.6154 61.54%
Glucocorticoid receptor binding - 0.5602 56.02%
Aromatase binding - 0.8111 81.11%
PPAR gamma - 0.8303 83.03%
Honey bee toxicity - 0.9052 90.52%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9974 99.74%

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 96.54% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.93% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.03% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.55% 91.11%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 84.00% 91.43%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.93% 97.09%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 83.69% 97.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.95% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.38% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.97% 93.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.79% 100.00%

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.
Ferula arrigonii
Ferula communis

Cross-Links

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PubChem 91748905
LOTUS LTS0159998
wikiData Q105385333