Circumdatin A

Details

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Internal ID fd29fd9c-40c9-4557-b084-a4f9088a2329
Taxonomy Organoheterocyclic compounds > Pyrimidodiazepines
IUPAC Name 10,18-dimethoxy-21-oxa-6,14,23-triazapentacyclo[12.9.0.02,6.08,13.016,22]tricosa-1(23),8(13),9,11,16(22),17,19-heptaene-7,15-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H19N3O5/c1-27-12-5-6-16-14(10-12)20(25)23-8-3-4-17(23)18-22-19-15(21(26)24(16)18)11-13(28-2)7-9-29-19/h5-7,9-11,17H,3-4,8H2,1-2H3
InChI Key YWIHZIZWXOCIAO-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H19N3O5
Molecular Weight 393.40 g/mol
Exact Mass 393.13247072 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.43
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Circumdatin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.7115 71.15%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6659 66.59%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8664 86.64%
OATP1B3 inhibitior + 0.9376 93.76%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.8942 89.42%
P-glycoprotein inhibitior + 0.8714 87.14%
P-glycoprotein substrate + 0.5580 55.80%
CYP3A4 substrate + 0.6868 68.68%
CYP2C9 substrate - 0.5894 58.94%
CYP2D6 substrate - 0.8402 84.02%
CYP3A4 inhibition - 0.7876 78.76%
CYP2C9 inhibition - 0.6839 68.39%
CYP2C19 inhibition - 0.6718 67.18%
CYP2D6 inhibition - 0.9152 91.52%
CYP1A2 inhibition + 0.6268 62.68%
CYP2C8 inhibition + 0.5460 54.60%
CYP inhibitory promiscuity - 0.6112 61.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6009 60.09%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.9763 97.63%
Skin irritation - 0.8142 81.42%
Skin corrosion - 0.9477 94.77%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6255 62.55%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.5626 56.26%
skin sensitisation - 0.8926 89.26%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.6158 61.58%
Acute Oral Toxicity (c) III 0.6974 69.74%
Estrogen receptor binding + 0.7998 79.98%
Androgen receptor binding + 0.7095 70.95%
Thyroid receptor binding + 0.7785 77.85%
Glucocorticoid receptor binding + 0.8894 88.94%
Aromatase binding + 0.5180 51.80%
PPAR gamma - 0.5703 57.03%
Honey bee toxicity - 0.9000 90.00%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.8612 86.12%

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
CHEMBL1951 P21397 Monoamine oxidase A 97.53% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.69% 94.00%
CHEMBL2581 P07339 Cathepsin D 95.24% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.80% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 93.28% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.01% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.63% 86.33%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 91.83% 98.46%
CHEMBL5203 P33316 dUTP pyrophosphatase 91.39% 99.18%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.73% 85.14%
CHEMBL230 P35354 Cyclooxygenase-2 90.13% 89.63%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.96% 97.09%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 89.45% 93.65%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.65% 93.99%
CHEMBL1907 P15144 Aminopeptidase N 88.34% 93.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.53% 99.23%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.36% 93.40%
CHEMBL226 P30542 Adenosine A1 receptor 85.88% 95.93%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 85.67% 92.67%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 85.23% 90.24%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 83.99% 95.53%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.38% 99.15%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.86% 82.69%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.64% 96.67%
CHEMBL4208 P20618 Proteasome component C5 82.64% 90.00%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 81.30% 91.43%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.71% 92.94%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 80.47% 95.78%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.22% 90.71%

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 74347666
LOTUS LTS0266867
wikiData Q104202145