Cangumycin B

Details

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Internal ID d5593ceb-ee4e-4d95-bd04-d1e0500cf537
Taxonomy Benzenoids > Tetralins
IUPAC Name (3S,6aR,7S,12aR)-6a,7,8-trihydroxy-3-methyl-3,4,7,12a-tetrahydro-2H-benzo[a]anthracene-1,12-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H18O5/c1-9-7-10-5-6-19(24)16(14(10)13(21)8-9)17(22)11-3-2-4-12(20)15(11)18(19)23/h2-6,9,16,18,20,23-24H,7-8H2,1H3/t9-,16-,18-,19+/m0/s1
InChI Key KINBEBQZPVMMJN-JEMNGFDGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O5
Molecular Weight 326.30 g/mol
Exact Mass 326.11542367 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 0.40
Atomic LogP (AlogP) 1.83
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cangumycin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9883 98.83%
Caco-2 - 0.6995 69.95%
Blood Brain Barrier - 0.6379 63.79%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7713 77.13%
OATP2B1 inhibitior - 0.7187 71.87%
OATP1B1 inhibitior + 0.9263 92.63%
OATP1B3 inhibitior + 0.9670 96.70%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9088 90.88%
BSEP inhibitior - 0.7103 71.03%
P-glycoprotein inhibitior - 0.8665 86.65%
P-glycoprotein substrate + 0.5084 50.84%
CYP3A4 substrate + 0.6296 62.96%
CYP2C9 substrate - 0.8006 80.06%
CYP2D6 substrate - 0.8613 86.13%
CYP3A4 inhibition - 0.8001 80.01%
CYP2C9 inhibition + 0.5207 52.07%
CYP2C19 inhibition - 0.7141 71.41%
CYP2D6 inhibition - 0.8142 81.42%
CYP1A2 inhibition + 0.6498 64.98%
CYP2C8 inhibition - 0.7894 78.94%
CYP inhibitory promiscuity - 0.6943 69.43%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9143 91.43%
Carcinogenicity (trinary) Non-required 0.5189 51.89%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.9519 95.19%
Skin irritation - 0.5790 57.90%
Skin corrosion - 0.8603 86.03%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6646 66.46%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.5447 54.47%
skin sensitisation - 0.5497 54.97%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.7168 71.68%
Acute Oral Toxicity (c) III 0.4623 46.23%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding + 0.6607 66.07%
Thyroid receptor binding - 0.6066 60.66%
Glucocorticoid receptor binding + 0.6954 69.54%
Aromatase binding - 0.5464 54.64%
PPAR gamma + 0.7486 74.86%
Honey bee toxicity - 0.9271 92.71%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9940 99.40%

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
CHEMBL1951 P21397 Monoamine oxidase A 98.68% 91.49%
CHEMBL2581 P07339 Cathepsin D 98.12% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.88% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.61% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 93.02% 94.75%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 92.41% 82.69%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.92% 99.23%
CHEMBL2535 P11166 Glucose transporter 90.56% 98.75%
CHEMBL221 P23219 Cyclooxygenase-1 90.47% 90.17%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 90.12% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.88% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.78% 97.09%
CHEMBL1907 P15144 Aminopeptidase N 88.04% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.41% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.78% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.71% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.65% 89.00%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 84.32% 96.00%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.23% 92.88%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.87% 99.15%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.60% 91.24%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.15% 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 146683608
LOTUS LTS0050256
wikiData Q105141600