Butyrate

Details

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Internal ID cbfb5d72-e20c-4c41-84be-76b92cacc2b8
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Straight chain fatty acids
IUPAC Name butanoate
SMILES (Canonical) CCCC(=O)[O-]
SMILES (Isomeric) CCCC(=O)[O-]
InChI InChI=1S/C4H8O2/c1-2-3-4(5)6/h2-3H2,1H3,(H,5,6)/p-1
InChI Key FERIUCNNQQJTOY-UHFFFAOYSA-M
Popularity 11,177 references in papers

Physical and Chemical Properties

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Molecular Formula C4H7O2-
Molecular Weight 87.10 g/mol
Exact Mass 87.044604462 g/mol
Topological Polar Surface Area (TPSA) 40.10 Ų
XlogP 1.40
Atomic LogP (AlogP) -0.46
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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butanoate
N-Butyrate
Butyrates
n-butanoate
Butanoic acid, ion(1-)
propylformate
461-55-2
butanate
1-butanoate
propanecarboxylate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Butyrate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9787 97.87%
Caco-2 + 0.8296 82.96%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Plasma membrane 0.5114 51.14%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.9267 92.67%
OATP1B3 inhibitior + 0.9320 93.20%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9359 93.59%
P-glycoprotein inhibitior - 0.9851 98.51%
P-glycoprotein substrate - 0.9771 97.71%
CYP3A4 substrate - 0.7726 77.26%
CYP2C9 substrate + 0.6276 62.76%
CYP2D6 substrate - 0.8931 89.31%
CYP3A4 inhibition - 0.9776 97.76%
CYP2C9 inhibition - 0.9151 91.51%
CYP2C19 inhibition - 0.9285 92.85%
CYP2D6 inhibition - 0.9492 94.92%
CYP1A2 inhibition - 0.5390 53.90%
CYP2C8 inhibition - 0.9857 98.57%
CYP inhibitory promiscuity - 0.9590 95.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5120 51.20%
Carcinogenicity (trinary) Non-required 0.5819 58.19%
Eye corrosion + 0.9951 99.51%
Eye irritation + 0.9948 99.48%
Skin irritation + 0.8550 85.50%
Skin corrosion + 0.6894 68.94%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8185 81.85%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6449 64.49%
skin sensitisation - 0.7953 79.53%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.4810 48.10%
Acute Oral Toxicity (c) III 0.7787 77.87%
Estrogen receptor binding - 0.9529 95.29%
Androgen receptor binding - 0.9612 96.12%
Thyroid receptor binding - 0.9306 93.06%
Glucocorticoid receptor binding - 0.9367 93.67%
Aromatase binding - 0.9218 92.18%
PPAR gamma - 0.9189 91.89%
Honey bee toxicity - 0.9778 97.78%
Biodegradation + 1.0000 100.00%
Crustacea aquatic toxicity - 0.7632 76.32%
Fish aquatic toxicity - 0.5443 54.43%

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 93.00% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.42% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.50% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.94% 99.17%

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.
Akebia quinata
Akebia trifoliata
Aloe africana
Aloe ferox
Aloe spicata
Aloe vera
Angelica acutiloba
Angelica gigas
Angelica sinensis

Cross-Links

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PubChem 104775
NPASS NPC149193