Rhinoclactone C

Details

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Internal ID e32e0bbc-7d8a-4515-8db6-c1abddaabd2b
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (4S,10R)-15-chloro-10,16-dihydroxy-18-methoxy-4-methyl-3-oxabicyclo[12.4.0]octadeca-1(18),14,16-triene-2,7,12-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H23ClO7/c1-10-3-4-11(21)5-6-12(22)7-13(23)8-14-17(19(25)27-10)16(26-2)9-15(24)18(14)20/h9-10,12,22,24H,3-8H2,1-2H3/t10-,12+/m0/s1
InChI Key FYSVSOAMDIXBBX-CMPLNLGQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H23ClO7
Molecular Weight 398.80 g/mol
Exact Mass 398.1132308 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.61
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Rhinoclactone C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 + 0.5730 57.30%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7124 71.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8941 89.41%
OATP1B3 inhibitior + 0.8930 89.30%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8071 80.71%
BSEP inhibitior + 0.6988 69.88%
P-glycoprotein inhibitior - 0.6843 68.43%
P-glycoprotein substrate - 0.7537 75.37%
CYP3A4 substrate + 0.6325 63.25%
CYP2C9 substrate - 0.7914 79.14%
CYP2D6 substrate - 0.8240 82.40%
CYP3A4 inhibition - 0.7159 71.59%
CYP2C9 inhibition - 0.8390 83.90%
CYP2C19 inhibition - 0.8390 83.90%
CYP2D6 inhibition - 0.9041 90.41%
CYP1A2 inhibition + 0.5797 57.97%
CYP2C8 inhibition - 0.5654 56.54%
CYP inhibitory promiscuity - 0.9477 94.77%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7505 75.05%
Carcinogenicity (trinary) Non-required 0.6005 60.05%
Eye corrosion - 0.9833 98.33%
Eye irritation - 0.9023 90.23%
Skin irritation - 0.7469 74.69%
Skin corrosion - 0.9153 91.53%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5908 59.08%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.7157 71.57%
skin sensitisation - 0.8451 84.51%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.6222 62.22%
Acute Oral Toxicity (c) II 0.3604 36.04%
Estrogen receptor binding + 0.7429 74.29%
Androgen receptor binding + 0.6152 61.52%
Thyroid receptor binding - 0.6008 60.08%
Glucocorticoid receptor binding + 0.8468 84.68%
Aromatase binding + 0.6207 62.07%
PPAR gamma + 0.6636 66.36%
Honey bee toxicity - 0.8371 83.71%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5151 51.51%
Fish aquatic toxicity + 0.9932 99.32%

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 99.51% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.92% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.07% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.44% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.39% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.67% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.98% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.63% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.51% 89.00%
CHEMBL2535 P11166 Glucose transporter 85.96% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.80% 93.99%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.53% 90.71%
CHEMBL217 P14416 Dopamine D2 receptor 85.34% 95.62%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.08% 97.14%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 83.22% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.01% 92.62%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.86% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.71% 99.17%
CHEMBL4208 P20618 Proteasome component C5 80.67% 90.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.58% 93.40%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.47% 91.07%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 80.25% 82.67%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 146682691
LOTUS LTS0003127
wikiData Q105004697