CID 72964398

Details

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Internal ID 605d5682-e6b3-4d2f-8fa7-780fe992ea02
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyrroloindoles
IUPAC Name 4-benzyl-9-(4-benzyl-5-methyl-3,6-dioxo-2,5,16-triazatetracyclo[7.7.0.02,7.010,15]hexadeca-10,12,14-trien-9-yl)-5-methyl-2,5,16-triazatetracyclo[7.7.0.02,7.010,15]hexadeca-10,12,14-triene-3,6-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H40N6O4/c1-45-31(21-25-13-5-3-6-14-25)37(51)47-33(35(45)49)23-41(27-17-9-11-19-29(27)43-39(41)47)42-24-34-36(50)46(2)32(22-26-15-7-4-8-16-26)38(52)48(34)40(42)44-30-20-12-10-18-28(30)42/h3-20,31-34,39-40,43-44H,21-24H2,1-2H3
InChI Key IQIGYVQQRKFGLN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C42H40N6O4
Molecular Weight 692.80 g/mol
Exact Mass 692.31110378 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 3.73
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 72964398

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9438 94.38%
Caco-2 - 0.7961 79.61%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6926 69.26%
OATP2B1 inhibitior + 0.7129 71.29%
OATP1B1 inhibitior + 0.9001 90.01%
OATP1B3 inhibitior + 0.9381 93.81%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7794 77.94%
BSEP inhibitior + 0.9844 98.44%
P-glycoprotein inhibitior + 0.8400 84.00%
P-glycoprotein substrate + 0.5699 56.99%
CYP3A4 substrate + 0.6094 60.94%
CYP2C9 substrate - 0.8149 81.49%
CYP2D6 substrate - 0.7957 79.57%
CYP3A4 inhibition - 0.7447 74.47%
CYP2C9 inhibition - 0.6191 61.91%
CYP2C19 inhibition - 0.6933 69.33%
CYP2D6 inhibition - 0.8506 85.06%
CYP1A2 inhibition - 0.8252 82.52%
CYP2C8 inhibition - 0.8428 84.28%
CYP inhibitory promiscuity - 0.7678 76.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6411 64.11%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9279 92.79%
Skin irritation - 0.7935 79.35%
Skin corrosion - 0.9379 93.79%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8864 88.64%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.8878 88.78%
Respiratory toxicity + 0.9222 92.22%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity + 0.6413 64.13%
Acute Oral Toxicity (c) III 0.5115 51.15%
Estrogen receptor binding + 0.7755 77.55%
Androgen receptor binding + 0.7770 77.70%
Thyroid receptor binding + 0.6280 62.80%
Glucocorticoid receptor binding + 0.6942 69.42%
Aromatase binding + 0.5331 53.31%
PPAR gamma + 0.7584 75.84%
Honey bee toxicity - 0.9053 90.53%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9302 93.02%

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 98.95% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.08% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.08% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.41% 95.56%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 87.62% 97.64%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.14% 93.00%
CHEMBL4208 P20618 Proteasome component C5 85.97% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.77% 94.45%
CHEMBL3524 P56524 Histone deacetylase 4 83.74% 92.97%
CHEMBL1937 Q92769 Histone deacetylase 2 82.82% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.46% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.34% 86.33%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.61% 90.08%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.74% 95.50%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.69% 96.25%
CHEMBL255 P29275 Adenosine A2b receptor 80.52% 98.59%

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 72964398
LOTUS LTS0094217
wikiData Q105117862