9-Hydroxyoudemansin A

Details

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Internal ID ed53b969-5bc4-45f2-a146-1b1f4431bf5e
Taxonomy Phenylpropanoids and polyketides > Cinnamyl alcohols
IUPAC Name methyl (E,2E,3R,4S)-4-hydroxy-2-(methoxymethylidene)-3-methyl-6-phenylhex-5-enoate
SMILES (Canonical) CC(C(C=CC1=CC=CC=C1)O)C(=COC)C(=O)OC
SMILES (Isomeric) C[C@@H]([C@H](/C=C/C1=CC=CC=C1)O)/C(=C\OC)/C(=O)OC
InChI InChI=1S/C16H20O4/c1-12(14(11-19-2)16(18)20-3)15(17)10-9-13-7-5-4-6-8-13/h4-12,15,17H,1-3H3/b10-9+,14-11+/t12-,15+/m1/s1
InChI Key REMSURQDUDTWHG-MIAXAGHPSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H20O4
Molecular Weight 276.33 g/mol
Exact Mass 276.13615911 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.40
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9-Hydroxyoudemansin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9842 98.42%
Caco-2 + 0.8879 88.79%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8058 80.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9147 91.47%
OATP1B3 inhibitior + 0.9536 95.36%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5308 53.08%
P-glycoprotein inhibitior - 0.6377 63.77%
P-glycoprotein substrate - 0.8722 87.22%
CYP3A4 substrate - 0.5839 58.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8482 84.82%
CYP3A4 inhibition - 0.8597 85.97%
CYP2C9 inhibition - 0.9294 92.94%
CYP2C19 inhibition - 0.8673 86.73%
CYP2D6 inhibition - 0.9546 95.46%
CYP1A2 inhibition - 0.9366 93.66%
CYP2C8 inhibition - 0.6928 69.28%
CYP inhibitory promiscuity - 0.7045 70.45%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) + 0.5027 50.27%
Carcinogenicity (trinary) Non-required 0.6804 68.04%
Eye corrosion - 0.9250 92.50%
Eye irritation - 0.6808 68.08%
Skin irritation - 0.6720 67.20%
Skin corrosion - 0.9967 99.67%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6915 69.15%
Micronuclear - 0.6400 64.00%
Hepatotoxicity - 0.5537 55.37%
skin sensitisation - 0.5678 56.78%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.4845 48.45%
Acute Oral Toxicity (c) III 0.5137 51.37%
Estrogen receptor binding + 0.5513 55.13%
Androgen receptor binding - 0.7491 74.91%
Thyroid receptor binding - 0.5616 56.16%
Glucocorticoid receptor binding - 0.7498 74.98%
Aromatase binding - 0.6903 69.03%
PPAR gamma - 0.7778 77.78%
Honey bee toxicity - 0.8208 82.08%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9323 93.23%

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
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.62% 96.00%
CHEMBL2581 P07339 Cathepsin D 94.16% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.11% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.04% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.96% 96.09%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 87.18% 94.08%
CHEMBL221 P23219 Cyclooxygenase-1 85.40% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 85.07% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.65% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.58% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.40% 86.33%
CHEMBL5028 O14672 ADAM10 84.33% 97.50%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.03% 100.00%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.48% 94.62%
CHEMBL4208 P20618 Proteasome component C5 82.35% 90.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.52% 93.56%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.42% 100.00%
CHEMBL2535 P11166 Glucose transporter 80.19% 98.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10754928
LOTUS LTS0247730
wikiData Q77386641