1,22-Docosanediol

Details

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Internal ID 3bed83ce-4449-4d5e-a08b-510234d0e091
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name docosane-1,22-diol
SMILES (Canonical) C(CCCCCCCCCCCO)CCCCCCCCCCO
SMILES (Isomeric) C(CCCCCCCCCCCO)CCCCCCCCCCO
InChI InChI=1S/C22H46O2/c23-21-19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18-20-22-24/h23-24H,1-22H2
InChI Key HIBKFQRBONXURO-UHFFFAOYSA-N
Popularity 19 references in papers

Physical and Chemical Properties

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Molecular Formula C22H46O2
Molecular Weight 342.60 g/mol
Exact Mass 342.349780706 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 9.00
Atomic LogP (AlogP) 6.77
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 21

Synonyms

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docosane-1,22-diol
22513-81-1
NSC405997
1,22-hexadecanediol
SCHEMBL472790
AMY038
CHEMBL470773
C(CCCCCCCCCCO)CCCCCCCCCCCO
DTXSID00324197
MFCD30470109
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,22-Docosanediol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9461 94.61%
Caco-2 - 0.6475 64.75%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.5544 55.44%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.9655 96.55%
OATP1B3 inhibitior + 0.9463 94.63%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8997 89.97%
P-glycoprotein inhibitior - 0.8848 88.48%
P-glycoprotein substrate - 0.9900 99.00%
CYP3A4 substrate - 0.8031 80.31%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6902 69.02%
CYP3A4 inhibition - 0.9700 97.00%
CYP2C9 inhibition - 0.8980 89.80%
CYP2C19 inhibition - 0.9491 94.91%
CYP2D6 inhibition - 0.9706 97.06%
CYP1A2 inhibition - 0.8671 86.71%
CYP2C8 inhibition - 0.9866 98.66%
CYP inhibitory promiscuity - 0.9440 94.40%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6204 62.04%
Eye corrosion + 0.9714 97.14%
Eye irritation + 0.9199 91.99%
Skin irritation - 0.5374 53.74%
Skin corrosion - 0.9481 94.81%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5879 58.79%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5368 53.68%
skin sensitisation + 0.5129 51.29%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.5955 59.55%
Acute Oral Toxicity (c) III 0.8566 85.66%
Estrogen receptor binding - 0.7680 76.80%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.6810 68.10%
Glucocorticoid receptor binding - 0.6395 63.95%
Aromatase binding - 0.6686 66.86%
PPAR gamma - 0.6373 63.73%
Honey bee toxicity - 0.9729 97.29%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.8284 82.84%
Fish aquatic toxicity - 0.9040 90.40%

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
CHEMBL2885 P07451 Carbonic anhydrase III 89.13% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.76% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.48% 97.29%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.38% 91.11%

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.
Codonopsis pilosula
Ficus carica
Hibiscus syriacus

Cross-Links

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PubChem 347359
NPASS NPC152759