Prezizaan-15-al

Details

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Internal ID 57f346f3-77fb-4ef6-8022-caefb4ebb139
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,2S,8R)-2,6,6-trimethyltricyclo[6.2.1.01,5]undecane-7-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-10-4-5-13-14(2,3)12(9-16)11-6-7-15(10,13)8-11/h9-13H,4-8H2,1-3H3/t10-,11+,12?,13?,15-/m0/s1
InChI Key FHSLAXWYMZHYPS-XILHMQAWSA-N
Popularity 2 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) 17.10 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.67
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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FHSLAXWYMZHYPS-XILHMQAWSA-N

2D Structure

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2D Structure of Prezizaan-15-al

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.6465 64.65%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.6735 67.35%
OATP2B1 inhibitior - 0.8512 85.12%
OATP1B1 inhibitior + 0.9293 92.93%
OATP1B3 inhibitior + 0.9554 95.54%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8640 86.40%
P-glycoprotein inhibitior - 0.8798 87.98%
P-glycoprotein substrate - 0.8853 88.53%
CYP3A4 substrate + 0.5455 54.55%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.7680 76.80%
CYP3A4 inhibition - 0.9393 93.93%
CYP2C9 inhibition - 0.8554 85.54%
CYP2C19 inhibition - 0.8900 89.00%
CYP2D6 inhibition - 0.9635 96.35%
CYP1A2 inhibition - 0.8105 81.05%
CYP2C8 inhibition - 0.8484 84.84%
CYP inhibitory promiscuity - 0.9146 91.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.6283 62.83%
Eye corrosion - 0.8486 84.86%
Eye irritation - 0.6317 63.17%
Skin irritation + 0.5665 56.65%
Skin corrosion - 0.9777 97.77%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5966 59.66%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5948 59.48%
skin sensitisation + 0.8301 83.01%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.5405 54.05%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.5856 58.56%
Acute Oral Toxicity (c) III 0.5395 53.95%
Estrogen receptor binding - 0.5271 52.71%
Androgen receptor binding - 0.6028 60.28%
Thyroid receptor binding - 0.6829 68.29%
Glucocorticoid receptor binding - 0.7612 76.12%
Aromatase binding - 0.6583 65.83%
PPAR gamma - 0.7621 76.21%
Honey bee toxicity - 0.6620 66.20%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.8000 80.00%
Fish aquatic toxicity + 0.9905 99.05%

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
CHEMBL233 P35372 Mu opioid receptor 87.22% 97.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.63% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.49% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 85.68% 90.17%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.36% 93.04%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.27% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.19% 82.69%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 83.53% 94.78%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.32% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.05% 95.56%
CHEMBL259 P32245 Melanocortin receptor 4 80.68% 95.38%

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 6428399
LOTUS LTS0216796
wikiData Q104667184