(3S)-hexan-3-ol

Details

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Internal ID df7c9e55-9bee-46bf-99a0-7e985d342982
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name (3S)-hexan-3-ol
SMILES (Canonical) CCCC(CC)O
SMILES (Isomeric) CCC[C@H](CC)O
InChI InChI=1S/C6H14O/c1-3-5-6(7)4-2/h6-7H,3-5H2,1-2H3/t6-/m0/s1
InChI Key ZOCHHNOQQHDWHG-LURJTMIESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C6H14O
Molecular Weight 102.17 g/mol
Exact Mass 102.104465066 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.56
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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(s)-hexan-3-ol
6210-51-1
Hexan-3S-ol
(3S)-3-Hexanol
SCHEMBL1462441
DTXSID40348539
LMFA05000463
EN300-6762808

2D Structure

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2D Structure of (3S)-hexan-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.8987 89.87%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.4228 42.28%
OATP2B1 inhibitior - 0.8414 84.14%
OATP1B1 inhibitior + 0.9475 94.75%
OATP1B3 inhibitior + 0.9247 92.47%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9446 94.46%
P-glycoprotein inhibitior - 0.9876 98.76%
P-glycoprotein substrate - 0.9452 94.52%
CYP3A4 substrate - 0.7743 77.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6625 66.25%
CYP3A4 inhibition - 0.9560 95.60%
CYP2C9 inhibition - 0.9191 91.91%
CYP2C19 inhibition - 0.9231 92.31%
CYP2D6 inhibition - 0.9205 92.05%
CYP1A2 inhibition + 0.6009 60.09%
CYP2C8 inhibition - 0.9941 99.41%
CYP inhibitory promiscuity - 0.8884 88.84%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.7288 72.88%
Eye corrosion + 0.8544 85.44%
Eye irritation + 0.9822 98.22%
Skin irritation + 0.6473 64.73%
Skin corrosion - 0.8585 85.85%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6360 63.60%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6662 66.62%
skin sensitisation + 0.9217 92.17%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.9037 90.37%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8788 87.88%
Estrogen receptor binding - 0.9098 90.98%
Androgen receptor binding - 0.9222 92.22%
Thyroid receptor binding - 0.8870 88.70%
Glucocorticoid receptor binding - 0.8877 88.77%
Aromatase binding - 0.9353 93.53%
PPAR gamma - 0.9269 92.69%
Honey bee toxicity - 0.9595 95.95%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity - 0.4808 48.08%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.42% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.38% 97.25%
CHEMBL2581 P07339 Cathepsin D 90.79% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 81.34% 90.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 81.27% 92.86%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 80.90% 98.75%

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.
Aloe africana
Aloe ferox
Aloe spicata
Aloe vera
Carthamus tinctorius

Cross-Links

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PubChem 638098
NPASS NPC30760