3-Hydroxyhexanoic acid

Details

Top
Internal ID ee3c65db-5512-4780-9841-40106de1c5f7
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name 3-hydroxyhexanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H12O3/c1-2-3-5(7)4-6(8)9/h5,7H,2-4H2,1H3,(H,8,9)
InChI Key HPMGFDVTYHWBAG-UHFFFAOYSA-N
Popularity 222 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H12O3
Molecular Weight 132.16 g/mol
Exact Mass 132.078644241 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.62
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

Top
10191-24-9
3-Hydroxycaproic acid
48NUX22XXO
FEMA NO. 5005
CHEBI:37035
DTXSID40906794
RefChem:502556
DTXCID701007909
3-HYDROXYHEXANOIC ACID, (A+-)-
600-248-5
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 3-Hydroxyhexanoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9106 91.06%
Caco-2 + 0.6982 69.82%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7286 72.86%
OATP2B1 inhibitior - 0.8482 84.82%
OATP1B1 inhibitior + 0.9495 94.95%
OATP1B3 inhibitior + 0.9320 93.20%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9572 95.72%
P-glycoprotein inhibitior - 0.9846 98.46%
P-glycoprotein substrate - 0.9513 95.13%
CYP3A4 substrate - 0.7301 73.01%
CYP2C9 substrate - 0.5774 57.74%
CYP2D6 substrate - 0.8588 85.88%
CYP3A4 inhibition - 0.9031 90.31%
CYP2C9 inhibition - 0.8572 85.72%
CYP2C19 inhibition - 0.8839 88.39%
CYP2D6 inhibition - 0.9219 92.19%
CYP1A2 inhibition - 0.6027 60.27%
CYP2C8 inhibition - 0.9968 99.68%
CYP inhibitory promiscuity - 0.8988 89.88%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8220 82.20%
Carcinogenicity (trinary) Non-required 0.6317 63.17%
Eye corrosion - 0.6608 66.08%
Eye irritation + 0.9770 97.70%
Skin irritation + 0.5140 51.40%
Skin corrosion + 0.7258 72.58%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7488 74.88%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.7940 79.40%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.7921 79.21%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.4941 49.41%
Acute Oral Toxicity (c) III 0.5919 59.19%
Estrogen receptor binding - 0.8987 89.87%
Androgen receptor binding - 0.9045 90.45%
Thyroid receptor binding - 0.8586 85.86%
Glucocorticoid receptor binding - 0.8668 86.68%
Aromatase binding - 0.8992 89.92%
PPAR gamma - 0.8319 83.19%
Honey bee toxicity - 0.9764 97.64%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity - 0.4509 45.09%

Targets

Top

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 96.01% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.60% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 88.40% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.22% 99.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.99% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.52% 93.56%

Plants that contains it

Top
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.
Solanum betaceum
Spondias mombin

Cross-Links

Top
PubChem 151492
LOTUS LTS0255045
wikiData Q27117019