Cyclotryprostatin G

Details

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Internal ID 9245b454-e8fa-433d-8197-914cde927db7
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Beta carbolines
IUPAC Name (1S,2S,12S,15S)-1-hydroxy-2-methoxy-12-(2-methylprop-1-enyl)-10,13,19-triazapentacyclo[11.7.0.03,11.04,9.015,19]icosa-3(11),4,6,8-tetraene-14,20-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H25N3O4/c1-12(2)11-16-18-17(13-7-4-5-8-14(13)23-18)19(29-3)22(28)21(27)24-10-6-9-15(24)20(26)25(16)22/h4-5,7-8,11,15-16,19,23,28H,6,9-10H2,1-3H3/t15-,16-,19-,22-/m0/s1
InChI Key QTOVUUPWQCFFQD-ZLFOXAAKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H25N3O4
Molecular Weight 395.50 g/mol
Exact Mass 395.18450629 g/mol
Topological Polar Surface Area (TPSA) 85.90 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.40
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cyclotryprostatin G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7874 78.74%
Caco-2 + 0.6273 62.73%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8357 83.57%
OATP2B1 inhibitior - 0.8574 85.74%
OATP1B1 inhibitior + 0.8764 87.64%
OATP1B3 inhibitior + 0.9214 92.14%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.7567 75.67%
BSEP inhibitior + 0.9539 95.39%
P-glycoprotein inhibitior + 0.6084 60.84%
P-glycoprotein substrate - 0.5280 52.80%
CYP3A4 substrate + 0.7091 70.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8396 83.96%
CYP3A4 inhibition - 0.7988 79.88%
CYP2C9 inhibition - 0.8150 81.50%
CYP2C19 inhibition - 0.8412 84.12%
CYP2D6 inhibition - 0.8937 89.37%
CYP1A2 inhibition - 0.6390 63.90%
CYP2C8 inhibition - 0.6475 64.75%
CYP inhibitory promiscuity - 0.6747 67.47%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5707 57.07%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9647 96.47%
Skin irritation - 0.7868 78.68%
Skin corrosion - 0.9398 93.98%
Ames mutagenesis - 0.6070 60.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5063 50.63%
Micronuclear + 0.7300 73.00%
Hepatotoxicity - 0.5705 57.05%
skin sensitisation - 0.8914 89.14%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.6843 68.43%
Acute Oral Toxicity (c) III 0.6032 60.32%
Estrogen receptor binding + 0.7106 71.06%
Androgen receptor binding + 0.7963 79.63%
Thyroid receptor binding - 0.5490 54.90%
Glucocorticoid receptor binding + 0.7011 70.11%
Aromatase binding + 0.6352 63.52%
PPAR gamma + 0.6503 65.03%
Honey bee toxicity - 0.6988 69.88%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.8429 84.29%

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 99.11% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.87% 91.11%
CHEMBL1902 P62942 FK506-binding protein 1A 96.93% 97.05%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.07% 96.09%
CHEMBL3524 P56524 Histone deacetylase 4 95.59% 92.97%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.56% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.21% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.10% 85.14%
CHEMBL5103 Q969S8 Histone deacetylase 10 93.38% 90.08%
CHEMBL1937 Q92769 Histone deacetylase 2 92.42% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.47% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.27% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.64% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.69% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.92% 97.09%
CHEMBL3310 Q96DB2 Histone deacetylase 11 85.64% 88.56%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.06% 93.03%
CHEMBL284 P27487 Dipeptidyl peptidase IV 83.52% 95.69%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.13% 92.94%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 82.31% 96.39%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 81.24% 82.38%
CHEMBL5028 O14672 ADAM10 80.98% 97.50%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.48% 92.67%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.33% 97.25%

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 146683049
LOTUS LTS0224967
wikiData Q105227848