Dienomycin C

Details

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Internal ID 2cdc8bc2-6051-499c-92ff-6f4c09eac6f9
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name (2R,3R,4S)-3-methyl-2-[(1E,3E)-4-phenylbuta-1,3-dienyl]piperidin-4-ol
SMILES (Canonical) CC1C(CCNC1C=CC=CC2=CC=CC=C2)O
SMILES (Isomeric) C[C@H]1[C@H](CCN[C@@H]1/C=C/C=C/C2=CC=CC=C2)O
InChI InChI=1S/C16H21NO/c1-13-15(17-12-11-16(13)18)10-6-5-9-14-7-3-2-4-8-14/h2-10,13,15-18H,11-12H2,1H3/b9-5+,10-6+/t13-,15-,16+/m1/s1
InChI Key BDDSGELKWZUGTC-UHNNFJLTSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H21NO
Molecular Weight 243.34 g/mol
Exact Mass 243.162314293 g/mol
Topological Polar Surface Area (TPSA) 32.30 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.61
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dienomycin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9788 97.88%
Caco-2 + 0.7650 76.50%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.5007 50.07%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8960 89.60%
OATP1B3 inhibitior + 0.9502 95.02%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.5750 57.50%
BSEP inhibitior - 0.7074 70.74%
P-glycoprotein inhibitior - 0.9435 94.35%
P-glycoprotein substrate - 0.7153 71.53%
CYP3A4 substrate - 0.5531 55.31%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate + 0.4758 47.58%
CYP3A4 inhibition - 0.8763 87.63%
CYP2C9 inhibition - 0.9158 91.58%
CYP2C19 inhibition - 0.8764 87.64%
CYP2D6 inhibition - 0.6215 62.15%
CYP1A2 inhibition - 0.8253 82.53%
CYP2C8 inhibition - 0.7725 77.25%
CYP inhibitory promiscuity - 0.9142 91.42%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6602 66.02%
Eye corrosion - 0.9565 95.65%
Eye irritation - 0.9707 97.07%
Skin irritation - 0.5648 56.48%
Skin corrosion - 0.6713 67.13%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6846 68.46%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.7716 77.16%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.8109 81.09%
Acute Oral Toxicity (c) III 0.6258 62.58%
Estrogen receptor binding - 0.6420 64.20%
Androgen receptor binding - 0.7843 78.43%
Thyroid receptor binding - 0.5202 52.02%
Glucocorticoid receptor binding - 0.7364 73.64%
Aromatase binding - 0.5828 58.28%
PPAR gamma + 0.5816 58.16%
Honey bee toxicity - 0.9279 92.79%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity - 0.9042 90.42%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.13% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.88% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.14% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.08% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.97% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 89.20% 90.17%
CHEMBL2581 P07339 Cathepsin D 84.70% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.93% 85.14%
CHEMBL5028 O14672 ADAM10 83.36% 97.50%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.24% 93.99%

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 49831773
LOTUS LTS0150903
wikiData Q104923966