(2S,8S)-5-propan-2-ylnonane-2,8-diol

Details

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Internal ID 90577722-5b1b-457b-a239-0880234d3d50
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (2S,8S)-5-propan-2-ylnonane-2,8-diol
SMILES (Canonical) CC(C)C(CCC(C)O)CCC(C)O
SMILES (Isomeric) C[C@@H](CCC(CC[C@H](C)O)C(C)C)O
InChI InChI=1S/C12H26O2/c1-9(2)12(7-5-10(3)13)8-6-11(4)14/h9-14H,5-8H2,1-4H3/t10-,11-/m0/s1
InChI Key UBXHRGCEAFKBFZ-QWRGUYRKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H26O2
Molecular Weight 202.33 g/mol
Exact Mass 202.193280068 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.58
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,8S)-5-propan-2-ylnonane-2,8-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.6906 69.06%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6228 62.28%
OATP2B1 inhibitior - 0.8460 84.60%
OATP1B1 inhibitior + 0.9644 96.44%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9770 97.70%
P-glycoprotein inhibitior - 0.9571 95.71%
P-glycoprotein substrate - 0.9396 93.96%
CYP3A4 substrate - 0.7484 74.84%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.6696 66.96%
CYP3A4 inhibition - 0.9331 93.31%
CYP2C9 inhibition - 0.9120 91.20%
CYP2C19 inhibition - 0.9262 92.62%
CYP2D6 inhibition - 0.9456 94.56%
CYP1A2 inhibition - 0.5970 59.70%
CYP2C8 inhibition - 0.9980 99.80%
CYP inhibitory promiscuity - 0.9270 92.70%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.7924 79.24%
Eye corrosion + 0.8300 83.00%
Eye irritation + 0.8928 89.28%
Skin irritation - 0.6640 66.40%
Skin corrosion - 0.9749 97.49%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6667 66.67%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5159 51.59%
skin sensitisation + 0.8787 87.87%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.8115 81.15%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity - 0.6168 61.68%
Acute Oral Toxicity (c) III 0.8927 89.27%
Estrogen receptor binding - 0.7994 79.94%
Androgen receptor binding - 0.8428 84.28%
Thyroid receptor binding - 0.4923 49.23%
Glucocorticoid receptor binding - 0.6068 60.68%
Aromatase binding - 0.8439 84.39%
PPAR gamma - 0.8676 86.76%
Honey bee toxicity - 0.9722 97.22%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.3669 36.69%

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
CHEMBL2581 P07339 Cathepsin D 92.91% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.29% 96.09%

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.
Nicotiana tabacum

Cross-Links

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PubChem 135390954
LOTUS LTS0241078
wikiData Q105269716