Desacetylanisomycin

Details

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Internal ID fbcdc3ba-0f86-43c4-920a-06defe449280
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name (2R,3R,4R)-2-[(4-methoxyphenyl)methyl]pyrrolidine-3,4-diol
SMILES (Canonical) COC1=CC=C(C=C1)CC2C(C(CN2)O)O
SMILES (Isomeric) COC1=CC=C(C=C1)C[C@@H]2[C@H]([C@@H](CN2)O)O
InChI InChI=1S/C12H17NO3/c1-16-9-4-2-8(3-5-9)6-10-12(15)11(14)7-13-10/h2-5,10-15H,6-7H2,1H3/t10-,11-,12-/m1/s1
InChI Key UMWAPBCLJQSOJX-IJLUTSLNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H17NO3
Molecular Weight 223.27 g/mol
Exact Mass 223.12084340 g/mol
Topological Polar Surface Area (TPSA) 61.70 Ų
XlogP 0.30
Atomic LogP (AlogP) -0.07
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Desacetylanisomycin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9501 95.01%
Caco-2 + 0.7466 74.66%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7649 76.49%
OATP2B1 inhibitior - 0.8626 86.26%
OATP1B1 inhibitior + 0.9562 95.62%
OATP1B3 inhibitior + 0.9545 95.45%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8870 88.70%
P-glycoprotein inhibitior - 0.9714 97.14%
P-glycoprotein substrate - 0.7844 78.44%
CYP3A4 substrate - 0.5155 51.55%
CYP2C9 substrate - 0.8132 81.32%
CYP2D6 substrate + 0.6786 67.86%
CYP3A4 inhibition - 0.9850 98.50%
CYP2C9 inhibition - 0.9221 92.21%
CYP2C19 inhibition - 0.8774 87.74%
CYP2D6 inhibition + 0.5665 56.65%
CYP1A2 inhibition - 0.9130 91.30%
CYP2C8 inhibition - 0.7607 76.07%
CYP inhibitory promiscuity - 0.8764 87.64%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6585 65.85%
Eye corrosion - 0.9842 98.42%
Eye irritation - 0.9341 93.41%
Skin irritation - 0.7036 70.36%
Skin corrosion - 0.8191 81.91%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7251 72.51%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.6233 62.33%
skin sensitisation - 0.8195 81.95%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.8932 89.32%
Acute Oral Toxicity (c) III 0.4655 46.55%
Estrogen receptor binding - 0.8307 83.07%
Androgen receptor binding - 0.7103 71.03%
Thyroid receptor binding - 0.7229 72.29%
Glucocorticoid receptor binding - 0.6628 66.28%
Aromatase binding - 0.6503 65.03%
PPAR gamma - 0.6614 66.14%
Honey bee toxicity - 0.9496 94.96%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.8924 89.24%

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 98.61% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.40% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.28% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.24% 97.09%
CHEMBL2581 P07339 Cathepsin D 91.41% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.94% 95.89%
CHEMBL4208 P20618 Proteasome component C5 90.56% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.84% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.73% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.45% 96.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.02% 92.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.70% 95.50%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.79% 93.99%
CHEMBL2535 P11166 Glucose transporter 82.12% 98.75%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.58% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.02% 99.17%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.68% 90.24%
CHEMBL226 P30542 Adenosine A1 receptor 80.44% 95.93%

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 11447409
LOTUS LTS0162756
wikiData Q77379734