2,3,4,5-Tetramethylhexane-1,2,3,4,5-pentol

Details

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Internal ID 7da6cb8b-8f9f-4bd2-b326-042562e500f5
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 2,3,4,5-tetramethylhexane-1,2,3,4,5-pentol
SMILES (Canonical) CC(C)(C(C)(C(C)(C(C)(CO)O)O)O)O
SMILES (Isomeric) CC(C)(C(C)(C(C)(C(C)(CO)O)O)O)O
InChI InChI=1S/C10H22O5/c1-7(2,12)9(4,14)10(5,15)8(3,13)6-11/h11-15H,6H2,1-5H3
InChI Key YNWGIYBRIPKRJK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H22O5
Molecular Weight 222.28 g/mol
Exact Mass 222.14672380 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP -1.80
Atomic LogP (AlogP) -1.00
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,3,4,5-Tetramethylhexane-1,2,3,4,5-pentol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7577 75.77%
Caco-2 + 0.5940 59.40%
Blood Brain Barrier + 0.6385 63.85%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5476 54.76%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.9386 93.86%
OATP1B3 inhibitior + 0.9369 93.69%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9470 94.70%
P-glycoprotein inhibitior - 0.9671 96.71%
P-glycoprotein substrate - 0.9639 96.39%
CYP3A4 substrate - 0.6619 66.19%
CYP2C9 substrate - 0.8348 83.48%
CYP2D6 substrate - 0.8084 80.84%
CYP3A4 inhibition - 0.8094 80.94%
CYP2C9 inhibition - 0.8605 86.05%
CYP2C19 inhibition - 0.8646 86.46%
CYP2D6 inhibition - 0.9314 93.14%
CYP1A2 inhibition - 0.8321 83.21%
CYP2C8 inhibition - 0.9832 98.32%
CYP inhibitory promiscuity - 0.9428 94.28%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.7243 72.43%
Eye corrosion - 0.9721 97.21%
Eye irritation + 0.7022 70.22%
Skin irritation - 0.6800 68.00%
Skin corrosion - 0.9788 97.88%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5688 56.88%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6594 65.94%
skin sensitisation - 0.7428 74.28%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.5935 59.35%
Acute Oral Toxicity (c) III 0.5030 50.30%
Estrogen receptor binding - 0.6252 62.52%
Androgen receptor binding - 0.6115 61.15%
Thyroid receptor binding - 0.6947 69.47%
Glucocorticoid receptor binding - 0.7046 70.46%
Aromatase binding - 0.6245 62.45%
PPAR gamma - 0.7609 76.09%
Honey bee toxicity - 0.9344 93.44%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity - 0.7650 76.50%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.39% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.87% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.98% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.63% 85.14%

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.
Cnidium monnieri

Cross-Links

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PubChem 45126424
LOTUS LTS0109367
wikiData Q105351136