Citreamicin theta B

Details

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Internal ID 0a4c5067-72be-4954-987a-f9889b539d5f
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name (7S,10S)-3,18,19,23-tetrahydroxy-7-(hydroxymethyl)-24-methoxy-7,10-dimethyl-9,28-dioxa-6-azaheptacyclo[15.12.0.02,14.04,12.06,10.020,29.022,27]nonacosa-1(17),2,4(12),13,18,20(29),22(27),23,25-nonaene-5,8,21-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H25NO11/c1-29(10-32)28(39)42-30(2)9-12-8-11-4-5-13-18(16(11)23(35)17(12)27(38)31(29)30)26-20(25(37)21(13)33)24(36)19-14(41-26)6-7-15(40-3)22(19)34/h6-8,32-35,37H,4-5,9-10H2,1-3H3/t29-,30-/m0/s1
InChI Key CELAFVAJJRUNHZ-KYJUHHDHSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C30H25NO11
Molecular Weight 575.50 g/mol
Exact Mass 575.14276061 g/mol
Topological Polar Surface Area (TPSA) 183.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 2.57
H-Bond Acceptor 11
H-Bond Donor 5
Rotatable Bonds 2

Synonyms

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CHEMBL4277938

2D Structure

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2D Structure of Citreamicin theta B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6329 63.29%
Caco-2 - 0.7870 78.70%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6570 65.70%
OATP2B1 inhibitior - 0.7122 71.22%
OATP1B1 inhibitior + 0.8721 87.21%
OATP1B3 inhibitior + 0.9204 92.04%
MATE1 inhibitior - 0.6400 64.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9181 91.81%
P-glycoprotein inhibitior + 0.6457 64.57%
P-glycoprotein substrate + 0.5336 53.36%
CYP3A4 substrate + 0.7047 70.47%
CYP2C9 substrate + 0.6319 63.19%
CYP2D6 substrate - 0.8510 85.10%
CYP3A4 inhibition - 0.7787 77.87%
CYP2C9 inhibition - 0.7677 76.77%
CYP2C19 inhibition - 0.8193 81.93%
CYP2D6 inhibition - 0.9237 92.37%
CYP1A2 inhibition - 0.8371 83.71%
CYP2C8 inhibition + 0.7349 73.49%
CYP inhibitory promiscuity - 0.8020 80.20%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5306 53.06%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.8978 89.78%
Skin irritation - 0.8012 80.12%
Skin corrosion - 0.9395 93.95%
Ames mutagenesis + 0.6236 62.36%
Human Ether-a-go-go-Related Gene inhibition - 0.6111 61.11%
Micronuclear + 0.7100 71.00%
Hepatotoxicity - 0.5046 50.46%
skin sensitisation - 0.8945 89.45%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.5438 54.38%
Acute Oral Toxicity (c) III 0.6047 60.47%
Estrogen receptor binding + 0.7401 74.01%
Androgen receptor binding + 0.7741 77.41%
Thyroid receptor binding + 0.5438 54.38%
Glucocorticoid receptor binding + 0.7452 74.52%
Aromatase binding + 0.6898 68.98%
PPAR gamma + 0.6909 69.09%
Honey bee toxicity - 0.7894 78.94%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5232 52.32%
Fish aquatic toxicity + 0.7540 75.40%

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 99.37% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.84% 94.45%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.79% 93.99%
CHEMBL2581 P07339 Cathepsin D 97.05% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.85% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.17% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.30% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.95% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.60% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.68% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.65% 95.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 87.51% 93.00%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 86.36% 95.53%
CHEMBL1255126 O15151 Protein Mdm4 86.08% 90.20%
CHEMBL4208 P20618 Proteasome component C5 85.76% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.93% 99.17%
CHEMBL3820 P35557 Hexokinase type IV 83.65% 91.96%
CHEMBL5555 O00767 Acyl-CoA desaturase 81.85% 97.50%
CHEMBL2535 P11166 Glucose transporter 81.62% 98.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.89% 96.95%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 80.83% 85.49%
CHEMBL3714531 Q6P988 Palmitoleoyl-protein carboxylesterase NOTUM 80.39% 97.14%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.36% 96.21%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.09% 92.62%

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 139586056
LOTUS LTS0171480
wikiData Q77497903