(Z,2E,3R,4S)-2-[(E)-but-2-enylidene]-3,4-dihydroxyhept-5-enal

Details

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Internal ID 112d52db-2f95-4844-8607-a545e8d51601
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (Z,2E,3R,4S)-2-[(E)-but-2-enylidene]-3,4-dihydroxyhept-5-enal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H16O3/c1-3-5-7-9(8-12)11(14)10(13)6-4-2/h3-8,10-11,13-14H,1-2H3/b5-3+,6-4-,9-7-/t10-,11+/m0/s1
InChI Key VPDVLNNSGPCYGT-DPCQOWFFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16O3
Molecular Weight 196.24 g/mol
Exact Mass 196.109944368 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.99
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z,2E,3R,4S)-2-[(E)-but-2-enylidene]-3,4-dihydroxyhept-5-enal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9771 97.71%
Caco-2 + 0.7000 70.00%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7109 71.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8844 88.44%
OATP1B3 inhibitior + 0.9640 96.40%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8516 85.16%
P-glycoprotein inhibitior - 0.9493 94.93%
P-glycoprotein substrate - 0.9503 95.03%
CYP3A4 substrate - 0.5846 58.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8449 84.49%
CYP3A4 inhibition - 0.8640 86.40%
CYP2C9 inhibition - 0.6714 67.14%
CYP2C19 inhibition - 0.8765 87.65%
CYP2D6 inhibition - 0.9282 92.82%
CYP1A2 inhibition - 0.8198 81.98%
CYP2C8 inhibition - 0.9720 97.20%
CYP inhibitory promiscuity - 0.8142 81.42%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) + 0.5577 55.77%
Carcinogenicity (trinary) Non-required 0.6452 64.52%
Eye corrosion + 0.6230 62.30%
Eye irritation - 0.6876 68.76%
Skin irritation + 0.6934 69.34%
Skin corrosion + 0.6156 61.56%
Ames mutagenesis + 0.5485 54.85%
Human Ether-a-go-go-Related Gene inhibition - 0.6592 65.92%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.6300 63.00%
skin sensitisation + 0.5381 53.81%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.8470 84.70%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.7351 73.51%
Acute Oral Toxicity (c) III 0.6673 66.73%
Estrogen receptor binding - 0.8952 89.52%
Androgen receptor binding - 0.9334 93.34%
Thyroid receptor binding - 0.6940 69.40%
Glucocorticoid receptor binding - 0.7248 72.48%
Aromatase binding - 0.8352 83.52%
PPAR gamma - 0.8540 85.40%
Honey bee toxicity - 0.6981 69.81%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity - 0.4740 47.40%

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 89.00% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.69% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.62% 95.56%

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.
Taxus brevifolia

Cross-Links

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PubChem 139583096
LOTUS LTS0274236
wikiData Q105290658