Chaetoglobosinf

Details

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Internal ID 7ee52236-00db-4bca-b4b4-e1b233c50215
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name 5-hydroxy-19-(1H-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.01,18.014,16]henicosa-7,11-diene-2,6,21-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H38N2O5/c1-17-8-7-10-22-29-31(4,39-29)19(3)27-24(15-20-16-33-23-11-6-5-9-21(20)23)34-30(38)32(22,27)26(36)13-12-25(35)28(37)18(2)14-17/h5-7,9-11,14,16-17,19,22,24-25,27,29,33,35H,8,12-13,15H2,1-4H3,(H,34,38)
InChI Key KTFGDHPTDQFFRL-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C32H38N2O5
Molecular Weight 530.70 g/mol
Exact Mass 530.27807232 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.06
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Chaetoglobosinf

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9697 96.97%
Caco-2 - 0.7876 78.76%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.4885 48.85%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.8584 85.84%
OATP1B3 inhibitior + 0.9319 93.19%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7343 73.43%
BSEP inhibitior + 0.9953 99.53%
P-glycoprotein inhibitior + 0.7986 79.86%
P-glycoprotein substrate + 0.6608 66.08%
CYP3A4 substrate + 0.7229 72.29%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8742 87.42%
CYP3A4 inhibition + 0.5168 51.68%
CYP2C9 inhibition - 0.7190 71.90%
CYP2C19 inhibition - 0.6954 69.54%
CYP2D6 inhibition - 0.8954 89.54%
CYP1A2 inhibition - 0.7658 76.58%
CYP2C8 inhibition + 0.6663 66.63%
CYP inhibitory promiscuity + 0.5898 58.98%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Danger 0.4304 43.04%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.9675 96.75%
Skin irritation - 0.7573 75.73%
Skin corrosion - 0.9214 92.14%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8428 84.28%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.5676 56.76%
skin sensitisation - 0.8397 83.97%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.6277 62.77%
Acute Oral Toxicity (c) II 0.5335 53.35%
Estrogen receptor binding + 0.7986 79.86%
Androgen receptor binding + 0.6785 67.85%
Thyroid receptor binding + 0.6498 64.98%
Glucocorticoid receptor binding + 0.8363 83.63%
Aromatase binding + 0.6372 63.72%
PPAR gamma + 0.7496 74.96%
Honey bee toxicity - 0.7112 71.12%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5053 50.53%
Fish aquatic toxicity + 0.8225 82.25%

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 99.50% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.18% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.92% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.51% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.97% 98.95%
CHEMBL3310 Q96DB2 Histone deacetylase 11 93.71% 88.56%
CHEMBL230 P35354 Cyclooxygenase-2 93.49% 89.63%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.34% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.73% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.03% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.80% 93.99%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.59% 92.62%
CHEMBL1937 Q92769 Histone deacetylase 2 91.55% 94.75%
CHEMBL213 P08588 Beta-1 adrenergic receptor 90.15% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.79% 97.09%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 88.98% 96.39%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.74% 100.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.64% 93.03%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.07% 92.94%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 86.03% 97.64%
CHEMBL3401 O75469 Pregnane X receptor 85.46% 94.73%
CHEMBL5805 Q9NR97 Toll-like receptor 8 84.91% 96.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.22% 86.33%
CHEMBL4530 P00488 Coagulation factor XIII 80.94% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.70% 95.89%
CHEMBL2996 Q05655 Protein kinase C delta 80.37% 97.79%

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 171477
LOTUS LTS0091738
wikiData Q105145763