3,7,11,15,19,23,27,31,35-Nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-ol

Details

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Internal ID f84a789c-5c90-4919-bd90-e3aea5aff6a9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Polyprenols
IUPAC Name 3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-ol
SMILES (Canonical) CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C
SMILES (Isomeric) CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C
InChI InChI=1S/C45H74O/c1-37(2)19-11-20-38(3)21-12-22-39(4)23-13-24-40(5)25-14-26-41(6)27-15-28-42(7)29-16-30-43(8)31-17-32-44(9)33-18-34-45(10)35-36-46/h19,21,23,25,27,29,31,33,35,46H,11-18,20,22,24,26,28,30,32,34,36H2,1-10H3
InChI Key AFPLNGZPBSKHHQ-UHFFFAOYSA-N
Popularity 62 references in papers

Physical and Chemical Properties

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Molecular Formula C45H74O
Molecular Weight 631.10 g/mol
Exact Mass 630.57396698 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 15.90
Atomic LogP (AlogP) 14.76
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 25

Synonyms

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NCGC00095707-03
FT-0602497
S0525
B0005-464623

2D Structure

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2D Structure of 3,7,11,15,19,23,27,31,35-Nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 - 0.7779 77.79%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.5576 55.76%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.9449 94.49%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9356 93.56%
P-glycoprotein inhibitior + 0.7259 72.59%
P-glycoprotein substrate - 0.9741 97.41%
CYP3A4 substrate - 0.6422 64.22%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.9088 90.88%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9026 90.26%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition - 0.9046 90.46%
CYP2C8 inhibition - 0.9772 97.72%
CYP inhibitory promiscuity - 0.7650 76.50%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6507 65.07%
Eye corrosion + 0.5325 53.25%
Eye irritation - 0.8379 83.79%
Skin irritation + 0.8492 84.92%
Skin corrosion - 0.9100 91.00%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3833 38.33%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.9375 93.75%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9812 98.12%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6319 63.19%
Acute Oral Toxicity (c) III 0.8552 85.52%
Estrogen receptor binding + 0.7714 77.14%
Androgen receptor binding - 0.7737 77.37%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.5770 57.70%
Aromatase binding - 0.5182 51.82%
PPAR gamma + 0.6927 69.27%
Honey bee toxicity - 0.9445 94.45%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9500 95.00%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.25% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.82% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.45% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.91% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.90% 99.17%

Cross-Links

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PubChem 83218
NPASS NPC256766
LOTUS LTS0019552
wikiData Q104911394