Emycine F

Details

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Internal ID c3fb2531-cdba-4fb5-aefe-8769677f2350
Taxonomy Benzenoids > Tetralins
IUPAC Name (1S,10R,17S)-17-methyl-2,19-dioxapentacyclo[8.8.1.11,11.04,9.015,20]icosa-4(9),5,7,11,13,15(20)-hexaene-5,12-diol
SMILES (Canonical) CC1CC2=C3C(=C(C=C2)O)C4C5=C(COC3(C1)O4)C(=CC=C5)O
SMILES (Isomeric) C[C@H]1CC2=C3C(=C(C=C2)O)[C@H]4C5=C(CO[C@@]3(C1)O4)C(=CC=C5)O
InChI InChI=1S/C19H18O4/c1-10-7-11-5-6-15(21)16-17(11)19(8-10)22-9-13-12(18(16)23-19)3-2-4-14(13)20/h2-6,10,18,20-21H,7-9H2,1H3/t10-,18+,19-/m0/s1
InChI Key GBIKCCXZTJUNIH-LDNBXIJLSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H18O4
Molecular Weight 310.30 g/mol
Exact Mass 310.12050905 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Emycine F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9838 98.38%
Caco-2 + 0.6917 69.17%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7812 78.12%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.9223 92.23%
OATP1B3 inhibitior + 0.9192 91.92%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.4826 48.26%
P-glycoprotein inhibitior - 0.8615 86.15%
P-glycoprotein substrate - 0.5676 56.76%
CYP3A4 substrate + 0.6115 61.15%
CYP2C9 substrate - 0.6012 60.12%
CYP2D6 substrate - 0.6701 67.01%
CYP3A4 inhibition - 0.7993 79.93%
CYP2C9 inhibition - 0.6107 61.07%
CYP2C19 inhibition - 0.5106 51.06%
CYP2D6 inhibition - 0.8278 82.78%
CYP1A2 inhibition - 0.5825 58.25%
CYP2C8 inhibition - 0.5983 59.83%
CYP inhibitory promiscuity - 0.7952 79.52%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.4927 49.27%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.9119 91.19%
Skin irritation - 0.8003 80.03%
Skin corrosion - 0.9623 96.23%
Ames mutagenesis + 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6793 67.93%
Micronuclear + 0.5400 54.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8399 83.99%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6288 62.88%
Acute Oral Toxicity (c) III 0.5739 57.39%
Estrogen receptor binding + 0.7017 70.17%
Androgen receptor binding + 0.6704 67.04%
Thyroid receptor binding + 0.6578 65.78%
Glucocorticoid receptor binding + 0.7899 78.99%
Aromatase binding + 0.6446 64.46%
PPAR gamma + 0.7702 77.02%
Honey bee toxicity - 0.8473 84.73%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9892 98.92%

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 98.93% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.48% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.28% 96.09%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 89.47% 96.39%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 89.13% 85.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.20% 86.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.84% 93.56%
CHEMBL2581 P07339 Cathepsin D 87.72% 98.95%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 86.01% 100.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.69% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.17% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.83% 97.09%
CHEMBL217 P14416 Dopamine D2 receptor 82.31% 95.62%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.76% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.40% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.23% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.21% 97.25%

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.
There are no matching plants.

Cross-Links

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PubChem 101038810
LOTUS LTS0030344
wikiData Q75058556