3-Hydroxy-butyraldehyde

Details

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Internal ID a8534bf2-1dc1-4060-95cd-e7823d3da971
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Beta-hydroxy aldehydes
IUPAC Name (3R)-3-hydroxybutanal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H8O2/c1-4(6)2-3-5/h3-4,6H,2H2,1H3/t4-/m1/s1
InChI Key HSJKGGMUJITCBW-SCSAIBSYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C4H8O2
Molecular Weight 88.11 g/mol
Exact Mass 88.052429494 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP -0.60
Atomic LogP (AlogP) -0.04
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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(3r)-3-Hydroxybutanal
RefChem:1067973
(r)-3-hydroxybutyraldehyde
SCHEMBL9027
SCHEMBL181898

2D Structure

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2D Structure of 3-Hydroxy-butyraldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.5548 55.48%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6486 64.86%
OATP2B1 inhibitior - 0.8695 86.95%
OATP1B1 inhibitior + 0.9397 93.97%
OATP1B3 inhibitior + 0.9599 95.99%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9509 95.09%
P-glycoprotein inhibitior - 0.9832 98.32%
P-glycoprotein substrate - 0.9805 98.05%
CYP3A4 substrate - 0.7702 77.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7548 75.48%
CYP3A4 inhibition - 0.9695 96.95%
CYP2C9 inhibition - 0.9736 97.36%
CYP2C19 inhibition - 0.8527 85.27%
CYP2D6 inhibition - 0.9430 94.30%
CYP1A2 inhibition - 0.7712 77.12%
CYP2C8 inhibition - 0.9964 99.64%
CYP inhibitory promiscuity - 0.9675 96.75%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) + 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.6832 68.32%
Eye corrosion + 0.9897 98.97%
Eye irritation + 0.9783 97.83%
Skin irritation + 0.8624 86.24%
Skin corrosion + 0.9136 91.36%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8168 81.68%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.5534 55.34%
skin sensitisation - 0.7899 78.99%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.4664 46.64%
Acute Oral Toxicity (c) III 0.7837 78.37%
Estrogen receptor binding - 0.9418 94.18%
Androgen receptor binding - 0.9220 92.20%
Thyroid receptor binding - 0.8605 86.05%
Glucocorticoid receptor binding - 0.9238 92.38%
Aromatase binding - 0.9095 90.95%
PPAR gamma - 0.8947 89.47%
Honey bee toxicity - 0.9553 95.53%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.9800 98.00%
Fish aquatic toxicity - 0.9157 91.57%

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 91.72% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.13% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 85.57% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.61% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.35% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 80.46% 94.73%

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.
Hymenophyton flabellatum

Cross-Links

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PubChem 13061653
LOTUS LTS0052123
wikiData Q105033086