Turbomycin A

Details

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Internal ID 31674768-55b3-4bdf-bc1e-505a2038c7c9
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles
IUPAC Name 3-[bis(1H-indol-3-yl)methylidene]indole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H17N3/c1-4-10-22-16(7-1)19(13-26-22)25(20-14-27-23-11-5-2-8-17(20)23)21-15-28-24-12-6-3-9-18(21)24/h1-15,26-27H
InChI Key ALYLUFTWTDPILH-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C25H17N3
Molecular Weight 359.40 g/mol
Exact Mass 359.142247555 g/mol
Topological Polar Surface Area (TPSA) 43.90 Ų
XlogP 5.30
Atomic LogP (AlogP) 6.32
H-Bond Acceptor 1
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 Turbomycin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.4914 49.14%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.3240 32.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9090 90.90%
OATP1B3 inhibitior + 0.9464 94.64%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.9241 92.41%
P-glycoprotein inhibitior - 0.6381 63.81%
P-glycoprotein substrate - 0.8292 82.92%
CYP3A4 substrate - 0.5155 51.55%
CYP2C9 substrate + 0.6176 61.76%
CYP2D6 substrate - 0.7601 76.01%
CYP3A4 inhibition + 0.6965 69.65%
CYP2C9 inhibition + 0.7340 73.40%
CYP2C19 inhibition + 0.6813 68.13%
CYP2D6 inhibition + 0.7020 70.20%
CYP1A2 inhibition + 0.9513 95.13%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.9787 97.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.6394 63.94%
Eye corrosion - 0.9798 97.98%
Eye irritation + 0.9358 93.58%
Skin irritation - 0.6138 61.38%
Skin corrosion - 0.9323 93.23%
Ames mutagenesis + 0.5430 54.30%
Human Ether-a-go-go-Related Gene inhibition - 0.4243 42.43%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7371 73.71%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.4584 45.84%
Acute Oral Toxicity (c) III 0.5260 52.60%
Estrogen receptor binding + 0.9816 98.16%
Androgen receptor binding + 0.7312 73.12%
Thyroid receptor binding + 0.8847 88.47%
Glucocorticoid receptor binding + 0.8963 89.63%
Aromatase binding + 0.9503 95.03%
PPAR gamma + 0.9340 93.40%
Honey bee toxicity - 0.9167 91.67%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9372 93.72%

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 93.64% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 92.55% 91.49%
CHEMBL6007 O75762 Transient receptor potential cation channel subfamily A member 1 91.36% 92.17%
CHEMBL2581 P07339 Cathepsin D 90.11% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.64% 95.56%
CHEMBL2535 P11166 Glucose transporter 88.49% 98.75%
CHEMBL3310 Q96DB2 Histone deacetylase 11 86.70% 88.56%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 85.62% 92.67%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 85.42% 85.49%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 84.85% 89.44%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.51% 94.00%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 84.31% 96.39%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.03% 96.67%
CHEMBL3902 P09211 Glutathione S-transferase Pi 82.69% 93.81%
CHEMBL213 P08588 Beta-1 adrenergic receptor 82.50% 95.56%
CHEMBL5805 Q9NR97 Toll-like receptor 8 82.37% 96.25%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 82.34% 96.47%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.01% 94.62%

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 13521337
LOTUS LTS0109263
wikiData Q104914436