5-hydroxy-15-[2-(1H-indol-3-yl)ethyl]-3,17,17-trimethyl-7-methylidene-15-azatricyclo[8.5.2.013,16]heptadeca-3,13(16)-dien-14-one

Details

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Internal ID 8bf53290-fed0-4ab2-a8ed-6c24ae049955
Taxonomy Phenylpropanoids and polyketides > Macrolactams
IUPAC Name 5-hydroxy-15-[2-(1H-indol-3-yl)ethyl]-3,17,17-trimethyl-7-methylidene-15-azatricyclo[8.5.2.013,16]heptadeca-3,13(16)-dien-14-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H38N2O2/c1-19-9-10-22-11-12-25-28(30(22,3)4)27(17-20(2)16-23(33)15-19)32(29(25)34)14-13-21-18-31-26-8-6-5-7-24(21)26/h5-8,16,18,22-23,27,31,33H,1,9-15,17H2,2-4H3
InChI Key ABTDHHPHHKFQBT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H38N2O2
Molecular Weight 458.60 g/mol
Exact Mass 458.293328459 g/mol
Topological Polar Surface Area (TPSA) 56.30 Ų
XlogP 5.00
Atomic LogP (AlogP) 6.09
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 5-hydroxy-15-[2-(1H-indol-3-yl)ethyl]-3,17,17-trimethyl-7-methylidene-15-azatricyclo[8.5.2.013,16]heptadeca-3,13(16)-dien-14-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 - 0.6443 64.43%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6725 67.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8636 86.36%
OATP1B3 inhibitior + 0.9315 93.15%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.9899 98.99%
P-glycoprotein inhibitior + 0.8302 83.02%
P-glycoprotein substrate + 0.6012 60.12%
CYP3A4 substrate + 0.7253 72.53%
CYP2C9 substrate - 0.6220 62.20%
CYP2D6 substrate - 0.8502 85.02%
CYP3A4 inhibition + 0.8590 85.90%
CYP2C9 inhibition - 0.6839 68.39%
CYP2C19 inhibition - 0.6159 61.59%
CYP2D6 inhibition - 0.8031 80.31%
CYP1A2 inhibition - 0.7575 75.75%
CYP2C8 inhibition + 0.4628 46.28%
CYP inhibitory promiscuity + 0.6670 66.70%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5403 54.03%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9579 95.79%
Skin irritation - 0.7699 76.99%
Skin corrosion - 0.9001 90.01%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7403 74.03%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8534 85.34%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.9054 90.54%
Acute Oral Toxicity (c) III 0.5619 56.19%
Estrogen receptor binding + 0.7975 79.75%
Androgen receptor binding + 0.5669 56.69%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7145 71.45%
Aromatase binding + 0.5981 59.81%
PPAR gamma + 0.6538 65.38%
Honey bee toxicity - 0.7693 76.93%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9874 98.74%

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 99.10% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.28% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.56% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.13% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.03% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.09% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.24% 85.14%
CHEMBL3310 Q96DB2 Histone deacetylase 11 90.80% 88.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.56% 99.23%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 90.54% 90.71%
CHEMBL5805 Q9NR97 Toll-like receptor 8 90.00% 96.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.37% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.52% 94.00%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 86.24% 96.39%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.91% 97.25%
CHEMBL5103 Q969S8 Histone deacetylase 10 85.76% 90.08%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.74% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.57% 93.03%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.40% 92.62%
CHEMBL1937 Q92769 Histone deacetylase 2 84.26% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.11% 86.33%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 83.01% 97.64%
CHEMBL4302 P08183 P-glycoprotein 1 81.18% 92.98%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.47% 100.00%

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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Cross-Links

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PubChem 162996651
LOTUS LTS0201229
wikiData Q104908820