Isotridecanol

Details

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Internal ID 479e44fb-d677-4f9a-9dc0-98eacaa94672
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 11-methyldodecan-1-ol
SMILES (Canonical) CC(C)CCCCCCCCCCO
SMILES (Isomeric) CC(C)CCCCCCCCCCO
InChI InChI=1S/C13H28O/c1-13(2)11-9-7-5-3-4-6-8-10-12-14/h13-14H,3-12H2,1-2H3
InChI Key XUJLWPFSUCHPQL-UHFFFAOYSA-N
Popularity 54 references in papers

Physical and Chemical Properties

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Molecular Formula C13H28O
Molecular Weight 200.36 g/mol
Exact Mass 200.214015512 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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11-Methyldodecanol
ISOTRIDECYL ALCOHOL
11-methyldodecan-1-ol
85763-57-1
Isotridecan-1-ol
27458-92-0
68526-86-3
Iso-Tridecyl-alcohol
Isotridecanol-
VX3T72M5SG
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isotridecanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.8504 85.04%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Lysosomes 0.6482 64.82%
OATP2B1 inhibitior - 0.8491 84.91%
OATP1B1 inhibitior + 0.9695 96.95%
OATP1B3 inhibitior + 0.9281 92.81%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7704 77.04%
P-glycoprotein inhibitior - 0.9538 95.38%
P-glycoprotein substrate - 0.9238 92.38%
CYP3A4 substrate - 0.7006 70.06%
CYP2C9 substrate - 0.8468 84.68%
CYP2D6 substrate - 0.7359 73.59%
CYP3A4 inhibition - 0.9449 94.49%
CYP2C9 inhibition - 0.8928 89.28%
CYP2C19 inhibition - 0.9404 94.04%
CYP2D6 inhibition - 0.9473 94.73%
CYP1A2 inhibition - 0.7547 75.47%
CYP2C8 inhibition - 0.9925 99.25%
CYP inhibitory promiscuity - 0.9468 94.68%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.7709 77.09%
Eye corrosion + 0.7993 79.93%
Eye irritation + 0.9728 97.28%
Skin irritation + 0.5985 59.85%
Skin corrosion - 0.9834 98.34%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6594 65.94%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5156 51.56%
skin sensitisation + 0.9577 95.77%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.9677 96.77%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.4830 48.30%
Acute Oral Toxicity (c) III 0.7514 75.14%
Estrogen receptor binding - 0.8625 86.25%
Androgen receptor binding - 0.8184 81.84%
Thyroid receptor binding + 0.5209 52.09%
Glucocorticoid receptor binding - 0.7713 77.13%
Aromatase binding - 0.8455 84.55%
PPAR gamma - 0.8576 85.76%
Honey bee toxicity - 0.9853 98.53%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.8229 82.29%
Fish aquatic toxicity + 0.7029 70.29%

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 95.39% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 93.35% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.56% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.20% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.26% 92.86%
CHEMBL1907 P15144 Aminopeptidase N 83.93% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.67% 99.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.54% 93.56%

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.
Vitis vinifera

Cross-Links

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PubChem 33865
LOTUS LTS0027553
wikiData Q27146966