2H-pyran

Details

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Internal ID f8dec21f-bf86-4f05-8a20-d1df0f516cac
Taxonomy Organoheterocyclic compounds > Pyrans
IUPAC Name 2H-pyran
SMILES (Canonical) C1C=CC=CO1
SMILES (Isomeric) C1C=CC=CO1
InChI InChI=1S/C5H6O/c1-2-4-6-5-3-1/h1-4H,5H2
InChI Key MGADZUXDNSDTHW-UHFFFAOYSA-N
Popularity 10,712 references in papers

Physical and Chemical Properties

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Molecular Formula C5H6O
Molecular Weight 82.10 g/mol
Exact Mass 82.041864811 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.09
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Pyran
1,2-Pyran
alpha-Pyran
CH5P2A5WTT
289-66-7
UNII-CH5P2A5WTT
31441-32-4
trans-pyran
pyran-
CHEBI:35592
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2H-pyran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.8780 87.80%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.4158 41.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9519 95.19%
OATP1B3 inhibitior + 0.9667 96.67%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9129 91.29%
P-glycoprotein inhibitior - 0.9889 98.89%
P-glycoprotein substrate - 0.9845 98.45%
CYP3A4 substrate - 0.7433 74.33%
CYP2C9 substrate + 0.6200 62.00%
CYP2D6 substrate - 0.7804 78.04%
CYP3A4 inhibition - 0.9663 96.63%
CYP2C9 inhibition - 0.8818 88.18%
CYP2C19 inhibition - 0.6995 69.95%
CYP2D6 inhibition - 0.9438 94.38%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.9705 97.05%
CYP inhibitory promiscuity - 0.7379 73.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6544 65.44%
Carcinogenicity (trinary) Warning 0.4656 46.56%
Eye corrosion + 0.9617 96.17%
Eye irritation + 0.9971 99.71%
Skin irritation + 0.9203 92.03%
Skin corrosion + 0.6288 62.88%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7647 76.47%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.5994 59.94%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6130 61.30%
Acute Oral Toxicity (c) III 0.6238 62.38%
Estrogen receptor binding - 0.9391 93.91%
Androgen receptor binding - 0.8517 85.17%
Thyroid receptor binding - 0.8956 89.56%
Glucocorticoid receptor binding - 0.7792 77.92%
Aromatase binding - 0.8782 87.82%
PPAR gamma - 0.8405 84.05%
Honey bee toxicity - 0.5408 54.08%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity - 0.6920 69.20%

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
No predicted targets yet!

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.
Wurfbainia neoaurantiaca

Cross-Links

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PubChem 186148
NPASS NPC46918