16,22-Dihydroxydocosan-3-one

Details

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Internal ID a7f14f26-8ff2-4c8d-9957-2a66d4a47918
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 16,22-dihydroxydocosan-3-one
SMILES (Canonical) CCC(=O)CCCCCCCCCCCCC(CCCCCCO)O
SMILES (Isomeric) CCC(=O)CCCCCCCCCCCCC(CCCCCCO)O
InChI InChI=1S/C22H44O3/c1-2-21(24)17-13-9-7-5-3-4-6-8-10-14-18-22(25)19-15-11-12-16-20-23/h22-23,25H,2-20H2,1H3
InChI Key DRBOQXGWUWINES-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H44O3
Molecular Weight 356.60 g/mol
Exact Mass 356.32904526 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 6.40
Atomic LogP (AlogP) 5.95
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 20

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 16,22-Dihydroxydocosan-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 - 0.6336 63.36%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7986 79.86%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.9425 94.25%
OATP1B3 inhibitior + 0.9356 93.56%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.6802 68.02%
P-glycoprotein inhibitior - 0.8284 82.84%
P-glycoprotein substrate - 0.8559 85.59%
CYP3A4 substrate - 0.6084 60.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7715 77.15%
CYP3A4 inhibition - 0.9009 90.09%
CYP2C9 inhibition - 0.8689 86.89%
CYP2C19 inhibition - 0.9353 93.53%
CYP2D6 inhibition - 0.9035 90.35%
CYP1A2 inhibition - 0.6336 63.36%
CYP2C8 inhibition - 0.9525 95.25%
CYP inhibitory promiscuity - 0.9034 90.34%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.7677 76.77%
Eye corrosion - 0.7345 73.45%
Eye irritation + 0.7575 75.75%
Skin irritation - 0.7980 79.80%
Skin corrosion - 0.9389 93.89%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4949 49.49%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6395 63.95%
skin sensitisation - 0.7620 76.20%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.8857 88.57%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.5525 55.25%
Acute Oral Toxicity (c) IV 0.5656 56.56%
Estrogen receptor binding - 0.7191 71.91%
Androgen receptor binding - 0.8479 84.79%
Thyroid receptor binding + 0.6028 60.28%
Glucocorticoid receptor binding - 0.5133 51.33%
Aromatase binding - 0.6672 66.72%
PPAR gamma + 0.5808 58.08%
Honey bee toxicity - 0.9616 96.16%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.7380 73.80%
Fish aquatic toxicity - 0.5311 53.11%

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 97.37% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 94.02% 97.29%
CHEMBL2581 P07339 Cathepsin D 93.55% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.19% 99.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.76% 100.00%
CHEMBL4040 P28482 MAP kinase ERK2 84.55% 83.82%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.98% 95.17%
CHEMBL2885 P07451 Carbonic anhydrase III 83.62% 87.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.66% 96.95%

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.
Cissus quadrangularis

Cross-Links

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PubChem 163189613
LOTUS LTS0123834
wikiData Q104987327