4-Hexen-1-ol, trifluoroacetate

Details

Top
Internal ID 3e1f71f2-5dfc-4a43-9e18-af777b6d40b4
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Alpha-halocarboxylic acids and derivatives > Alpha-halocarboxylic acid derivatives
IUPAC Name [(E)-hex-4-enyl] 2,2,2-trifluoroacetate
SMILES (Canonical) CC=CCCCOC(=O)C(F)(F)F
SMILES (Isomeric) C/C=C/CCCOC(=O)C(F)(F)F
InChI InChI=1S/C8H11F3O2/c1-2-3-4-5-6-13-7(12)8(9,10)11/h2-3H,4-6H2,1H3/b3-2+
InChI Key VGZQUSPVQQXMSU-NSCUHMNNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C8H11F3O2
Molecular Weight 196.17 g/mol
Exact Mass 196.07111408 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
VGZQUSPVQQXMSU-NSCUHMNNSA-N

2D Structure

Top
2D Structure of 4-Hexen-1-ol, trifluoroacetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.7247 72.47%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7571 75.71%
OATP2B1 inhibitior - 0.8513 85.13%
OATP1B1 inhibitior + 0.8537 85.37%
OATP1B3 inhibitior + 0.9327 93.27%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8813 88.13%
P-glycoprotein inhibitior - 0.9749 97.49%
P-glycoprotein substrate - 0.9692 96.92%
CYP3A4 substrate - 0.5323 53.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8144 81.44%
CYP3A4 inhibition - 0.9215 92.15%
CYP2C9 inhibition - 0.8966 89.66%
CYP2C19 inhibition - 0.7968 79.68%
CYP2D6 inhibition - 0.9236 92.36%
CYP1A2 inhibition + 0.5721 57.21%
CYP2C8 inhibition - 0.8602 86.02%
CYP inhibitory promiscuity - 0.8833 88.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5907 59.07%
Carcinogenicity (trinary) Non-required 0.5657 56.57%
Eye corrosion + 0.9189 91.89%
Eye irritation + 0.8841 88.41%
Skin irritation - 0.6602 66.02%
Skin corrosion - 0.9540 95.40%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5140 51.40%
Micronuclear - 0.8326 83.26%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.9137 91.37%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.7278 72.78%
Acute Oral Toxicity (c) I 0.4892 48.92%
Estrogen receptor binding - 0.9430 94.30%
Androgen receptor binding - 0.8774 87.74%
Thyroid receptor binding - 0.8839 88.39%
Glucocorticoid receptor binding - 0.7473 74.73%
Aromatase binding - 0.8150 81.50%
PPAR gamma - 0.8198 81.98%
Honey bee toxicity - 0.9137 91.37%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8334 83.34%

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 95.14% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.33% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.96% 97.25%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.64% 89.34%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 84.09% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 81.86% 94.73%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 80.28% 92.95%

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.
Mentha arvensis
Mentha canadensis

Cross-Links

Top
PubChem 91694359
NPASS NPC43493