12-(5-Hydroxy-6-methyl-2-pyridinyl)dodecane-1,6-diol

Details

Top
Internal ID 947aa0cd-a4cb-44ea-9527-4003e8f67a2b
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Methylpyridines
IUPAC Name 12-(5-hydroxy-6-methyl-2-pyridinyl)dodecane-1,6-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H31NO3/c1-15-18(22)13-12-16(19-15)9-5-2-3-6-10-17(21)11-7-4-8-14-20/h12-13,17,20-22H,2-11,14H2,1H3
InChI Key NVCDYIVRRNILOL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H31NO3
Molecular Weight 309.40 g/mol
Exact Mass 309.23039385 g/mol
Topological Polar Surface Area (TPSA) 73.60 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.50
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 12

Synonyms

Top
CHEMBL2022770

2D Structure

Top
2D Structure of 12-(5-Hydroxy-6-methyl-2-pyridinyl)dodecane-1,6-diol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9927 99.27%
Caco-2 + 0.6205 62.05%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8991 89.91%
OATP2B1 inhibitior - 0.8520 85.20%
OATP1B1 inhibitior + 0.9496 94.96%
OATP1B3 inhibitior + 0.9407 94.07%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.4695 46.95%
P-glycoprotein inhibitior - 0.8997 89.97%
P-glycoprotein substrate - 0.7564 75.64%
CYP3A4 substrate - 0.5294 52.94%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7106 71.06%
CYP3A4 inhibition - 0.7255 72.55%
CYP2C9 inhibition - 0.8963 89.63%
CYP2C19 inhibition - 0.8407 84.07%
CYP2D6 inhibition - 0.9343 93.43%
CYP1A2 inhibition - 0.8074 80.74%
CYP2C8 inhibition - 0.7540 75.40%
CYP inhibitory promiscuity - 0.8321 83.21%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.7335 73.35%
Eye corrosion - 0.9804 98.04%
Eye irritation - 0.8391 83.91%
Skin irritation - 0.7043 70.43%
Skin corrosion - 0.9126 91.26%
Ames mutagenesis - 0.8154 81.54%
Human Ether-a-go-go-Related Gene inhibition + 0.8939 89.39%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.5706 57.06%
skin sensitisation - 0.7645 76.45%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.5659 56.59%
Acute Oral Toxicity (c) III 0.7900 79.00%
Estrogen receptor binding + 0.7601 76.01%
Androgen receptor binding - 0.6056 60.56%
Thyroid receptor binding + 0.7325 73.25%
Glucocorticoid receptor binding - 0.5791 57.91%
Aromatase binding - 0.6274 62.74%
PPAR gamma + 0.7643 76.43%
Honey bee toxicity - 0.9737 97.37%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7301 73.01%
Fish aquatic toxicity - 0.9207 92.07%

Targets

Top

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
CHEMBL2581 P07339 Cathepsin D 94.01% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.77% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 90.95% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.24% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.87% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.46% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 84.37% 87.45%
CHEMBL1951 P21397 Monoamine oxidase A 83.93% 91.49%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.58% 96.90%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 81.43% 92.68%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.70% 96.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.60% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 80.43% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.04% 86.33%

Plants that contains it

Top
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.
Senna multijuga

Cross-Links

Top
PubChem 57382622
LOTUS LTS0214825
wikiData Q105186151