2-Penten-1-OL

Details

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Internal ID c7e539b0-f9a6-43dd-91bc-ad36e3afa8a9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name (E)-pent-2-en-1-ol
SMILES (Canonical) CCC=CCO
SMILES (Isomeric) CC/C=C/CO
InChI InChI=1S/C5H10O/c1-2-3-4-5-6/h3-4,6H,2,5H2,1H3/b4-3+
InChI Key BTSIZIIPFNVMHF-ONEGZZNKSA-N
Popularity 114 references in papers

Physical and Chemical Properties

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Molecular Formula C5H10O
Molecular Weight 86.13 g/mol
Exact Mass 86.073164938 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.94
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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(E)-Pent-2-en-1-ol
2-PENTEN-1-OL
1576-96-1
trans-2-pentenol
(E)-2-pentenol
2-Penten-1-ol, (E)-
(2E)-2-Penten-1-ol
2-Penten-1-ol, (2E)-
20273-24-9
2-pentenol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Penten-1-OL

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9839 98.39%
Caco-2 + 0.8822 88.22%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.5591 55.91%
OATP2B1 inhibitior - 0.8618 86.18%
OATP1B1 inhibitior + 0.9168 91.68%
OATP1B3 inhibitior + 0.9381 93.81%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9279 92.79%
P-glycoprotein inhibitior - 0.9855 98.55%
P-glycoprotein substrate - 0.9848 98.48%
CYP3A4 substrate - 0.7865 78.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9388 93.88%
CYP2C9 inhibition - 0.8891 88.91%
CYP2C19 inhibition - 0.8931 89.31%
CYP2D6 inhibition - 0.9421 94.21%
CYP1A2 inhibition - 0.6559 65.59%
CYP2C8 inhibition - 0.9873 98.73%
CYP inhibitory promiscuity - 0.7102 71.02%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.5329 53.29%
Eye corrosion + 0.9191 91.91%
Eye irritation + 0.9846 98.46%
Skin irritation + 0.7438 74.38%
Skin corrosion - 0.8467 84.67%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6901 69.01%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.7229 72.29%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.6209 62.09%
Acute Oral Toxicity (c) III 0.7636 76.36%
Estrogen receptor binding - 0.9626 96.26%
Androgen receptor binding - 0.9382 93.82%
Thyroid receptor binding - 0.9281 92.81%
Glucocorticoid receptor binding - 0.9037 90.37%
Aromatase binding - 0.9089 90.89%
PPAR gamma - 0.9018 90.18%
Honey bee toxicity - 0.9790 97.90%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity - 0.3781 37.81%

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 86.66% 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.
Capsicum annuum
Perilla frutescens
Vitis vinifera

Cross-Links

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PubChem 5364920
NPASS NPC119049
LOTUS LTS0003505
wikiData Q27260874