Cyclopiamide J

Details

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Internal ID c0a6cf34-6b1b-40c0-9d0c-745f089275ef
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name (1R,2R,3S,4R,5S,9R)-3,4,5-trihydroxy-8,8,16-trimethyl-5-(2-oxopropyl)-19-oxa-7,16-diazahexacyclo[9.6.1.11,4.02,9.03,7.015,18]nonadeca-11(18),12,14-triene-6,17-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H24N2O7/c1-10(25)9-19(28)16(26)24-18(2,3)12-8-11-6-5-7-13-14(11)20(17(27)23(13)4)15(12)21(24,29)22(19,30)31-20/h5-7,12,15,28-30H,8-9H2,1-4H3/t12-,15-,19-,20+,21+,22-/m1/s1
InChI Key SECNHDOFHUTKGZ-UEYCCITJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H24N2O7
Molecular Weight 428.40 g/mol
Exact Mass 428.15835111 g/mol
Topological Polar Surface Area (TPSA) 128.00 Ų
XlogP -1.20
Atomic LogP (AlogP) -0.60
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cyclopiamide J

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5471 54.71%
Caco-2 - 0.5703 57.03%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.3968 39.68%
OATP2B1 inhibitior - 0.8477 84.77%
OATP1B1 inhibitior + 0.8823 88.23%
OATP1B3 inhibitior + 0.9317 93.17%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8143 81.43%
P-glycoprotein inhibitior - 0.5740 57.40%
P-glycoprotein substrate + 0.5146 51.46%
CYP3A4 substrate + 0.6781 67.81%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.8492 84.92%
CYP3A4 inhibition - 0.8238 82.38%
CYP2C9 inhibition - 0.8436 84.36%
CYP2C19 inhibition - 0.8298 82.98%
CYP2D6 inhibition - 0.9177 91.77%
CYP1A2 inhibition - 0.7825 78.25%
CYP2C8 inhibition - 0.7324 73.24%
CYP inhibitory promiscuity - 0.8648 86.48%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5204 52.04%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9292 92.92%
Skin irritation - 0.7863 78.63%
Skin corrosion - 0.9295 92.95%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3671 36.71%
Micronuclear + 0.8000 80.00%
Hepatotoxicity - 0.5084 50.84%
skin sensitisation - 0.8639 86.39%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.6501 65.01%
Acute Oral Toxicity (c) III 0.6288 62.88%
Estrogen receptor binding + 0.6561 65.61%
Androgen receptor binding + 0.7381 73.81%
Thyroid receptor binding + 0.5755 57.55%
Glucocorticoid receptor binding + 0.6430 64.30%
Aromatase binding + 0.6301 63.01%
PPAR gamma + 0.6263 62.63%
Honey bee toxicity - 0.8685 86.85%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.8886 88.86%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.89% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.85% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.86% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.26% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.38% 95.56%
CHEMBL217 P14416 Dopamine D2 receptor 91.67% 95.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.62% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.57% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.12% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.44% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.83% 100.00%

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 122218859
LOTUS LTS0170129
wikiData Q77424466