Anhydrocyanobacterin

Details

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Internal ID 5a7abdc3-7804-4dd7-997d-e883b269638b
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name 3-[(7-chloro-1,3-benzodioxol-5-yl)methyl]-5-[(4-methoxyphenyl)methylidene]-4-propan-2-ylfuran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H21ClO5/c1-13(2)21-17(8-15-9-18(24)22-20(11-15)27-12-28-22)23(25)29-19(21)10-14-4-6-16(26-3)7-5-14/h4-7,9-11,13H,8,12H2,1-3H3
InChI Key GNRHIDBFAWGJDI-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H21ClO5
Molecular Weight 412.90 g/mol
Exact Mass 412.1077515 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.17
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Anhydrocyanobacterin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 + 0.6770 67.70%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6848 68.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9093 90.93%
OATP1B3 inhibitior + 0.9344 93.44%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9856 98.56%
P-glycoprotein inhibitior + 0.8299 82.99%
P-glycoprotein substrate - 0.8471 84.71%
CYP3A4 substrate + 0.6270 62.70%
CYP2C9 substrate - 0.5895 58.95%
CYP2D6 substrate - 0.8603 86.03%
CYP3A4 inhibition + 0.9572 95.72%
CYP2C9 inhibition + 0.8642 86.42%
CYP2C19 inhibition + 0.8935 89.35%
CYP2D6 inhibition - 0.5281 52.81%
CYP1A2 inhibition + 0.7013 70.13%
CYP2C8 inhibition - 0.5985 59.85%
CYP inhibitory promiscuity + 0.9760 97.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8438 84.38%
Carcinogenicity (trinary) Danger 0.4753 47.53%
Eye corrosion - 0.9856 98.56%
Eye irritation - 0.9390 93.90%
Skin irritation - 0.7808 78.08%
Skin corrosion - 0.9241 92.41%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7529 75.29%
Micronuclear - 0.5193 51.93%
Hepatotoxicity - 0.5585 55.85%
skin sensitisation - 0.6609 66.09%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.6494 64.94%
Acute Oral Toxicity (c) III 0.5209 52.09%
Estrogen receptor binding + 0.8987 89.87%
Androgen receptor binding + 0.7845 78.45%
Thyroid receptor binding + 0.5884 58.84%
Glucocorticoid receptor binding + 0.8691 86.91%
Aromatase binding + 0.5635 56.35%
PPAR gamma + 0.8297 82.97%
Honey bee toxicity - 0.7168 71.68%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.7547 75.47%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 99.63% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.82% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.67% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.63% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.32% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 94.79% 92.62%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 94.44% 94.80%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.00% 86.33%
CHEMBL4208 P20618 Proteasome component C5 93.88% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 93.46% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.73% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.71% 96.00%
CHEMBL5957 P21589 5'-nucleotidase 90.48% 97.78%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.21% 95.50%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.36% 99.15%
CHEMBL221 P23219 Cyclooxygenase-1 88.16% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.00% 95.89%
CHEMBL1929 P47989 Xanthine dehydrogenase 87.11% 96.12%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.37% 93.99%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.06% 90.24%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.33% 90.71%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.57% 95.17%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.35% 91.07%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.09% 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 163000127
LOTUS LTS0270202
wikiData Q105013151