[(1S,4E,6R,10R,12E,14R,15S,17S,18S,19S)-19-benzyl-6-hydroxy-10,17-dimethyl-16-methylidene-3,21-dioxo-2-oxa-20-azatricyclo[12.7.0.01,18]henicosa-4,12-dien-15-yl] acetate

Details

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Internal ID 4129497f-2c71-49a2-a74b-fa0cffb2bc7b
Taxonomy Organoheterocyclic compounds > Isoindoles and derivatives > Isoindoles
IUPAC Name [(1S,4E,6R,10R,12E,14R,15S,17S,18S,19S)-19-benzyl-6-hydroxy-10,17-dimethyl-16-methylidene-3,21-dioxo-2-oxa-20-azatricyclo[12.7.0.01,18]henicosa-4,12-dien-15-yl] acetate
SMILES (Canonical) CC1CCCC(C=CC(=O)OC23C(C=CC1)C(C(=C)C(C2C(NC3=O)CC4=CC=CC=C4)C)OC(=O)C)O
SMILES (Isomeric) C[C@@H]1CCC[C@H](/C=C/C(=O)O[C@]23[C@H](/C=C/C1)[C@@H](C(=C)[C@H]([C@H]2[C@@H](NC3=O)CC4=CC=CC=C4)C)OC(=O)C)O
InChI InChI=1S/C31H39NO6/c1-19-10-8-14-24(34)16-17-27(35)38-31-25(15-9-11-19)29(37-22(4)33)21(3)20(2)28(31)26(32-30(31)36)18-23-12-6-5-7-13-23/h5-7,9,12-13,15-17,19-20,24-26,28-29,34H,3,8,10-11,14,18H2,1-2,4H3,(H,32,36)/b15-9+,17-16+/t19-,20-,24-,25-,26+,28+,29-,31-/m1/s1
InChI Key GCERPZSZVAOMGR-OLRGGGCCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H39NO6
Molecular Weight 521.60 g/mol
Exact Mass 521.27773796 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.06
H-Bond Acceptor 6
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 [(1S,4E,6R,10R,12E,14R,15S,17S,18S,19S)-19-benzyl-6-hydroxy-10,17-dimethyl-16-methylidene-3,21-dioxo-2-oxa-20-azatricyclo[12.7.0.01,18]henicosa-4,12-dien-15-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9726 97.26%
Caco-2 - 0.8382 83.82%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Plasma membrane 0.4644 46.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8042 80.42%
OATP1B3 inhibitior + 0.8846 88.46%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7322 73.22%
BSEP inhibitior + 0.8843 88.43%
P-glycoprotein inhibitior - 0.4421 44.21%
P-glycoprotein substrate + 0.6644 66.44%
CYP3A4 substrate + 0.7179 71.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8884 88.84%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.8264 82.64%
CYP2C19 inhibition - 0.7813 78.13%
CYP2D6 inhibition - 0.9292 92.92%
CYP1A2 inhibition - 0.8528 85.28%
CYP2C8 inhibition + 0.7089 70.89%
CYP inhibitory promiscuity + 0.5054 50.54%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Danger 0.4551 45.51%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9466 94.66%
Skin irritation - 0.6960 69.60%
Skin corrosion - 0.9279 92.79%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3790 37.90%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.5585 55.85%
skin sensitisation - 0.8440 84.40%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.5728 57.28%
Acute Oral Toxicity (c) III 0.4668 46.68%
Estrogen receptor binding + 0.7033 70.33%
Androgen receptor binding + 0.6563 65.63%
Thyroid receptor binding - 0.5222 52.22%
Glucocorticoid receptor binding + 0.8100 81.00%
Aromatase binding + 0.5828 58.28%
PPAR gamma + 0.7494 74.94%
Honey bee toxicity - 0.7004 70.04%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9870 98.70%

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
CHEMBL2581 P07339 Cathepsin D 99.58% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.55% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.39% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.03% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.49% 94.45%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.68% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.64% 86.33%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 89.01% 97.64%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.49% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.90% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.38% 95.89%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.56% 94.62%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.15% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.91% 99.23%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.17% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.50% 89.00%
CHEMBL4208 P20618 Proteasome component C5 80.34% 90.00%

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 163186391
LOTUS LTS0006220
wikiData Q105006249