Kadcoccilactone L

Details

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Internal ID f50faf11-2893-4780-a8e1-9567bd197bbb
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name (1R,2S,5R,13S,15R,26R)-13,26-dihydroxy-1,6,6,20,24-pentamethyl-7,22-dioxahexacyclo[13.12.0.02,13.05,11.016,25.018,23]heptacosa-9,11,16(25),17,19,23-hexaene-8,21-dione
SMILES (Canonical) CC1=CC2=CC3=C(C(CC4(C3CC5(C4CCC6C(=C5)C=CC(=O)OC6(C)C)O)C)O)C(=C2OC1=O)C
SMILES (Isomeric) CC1=CC2=CC3=C([C@@H](C[C@@]4([C@H]3C[C@]5([C@H]4CC[C@@H]6C(=C5)C=CC(=O)OC6(C)C)O)C)O)C(=C2OC1=O)C
InChI InChI=1S/C30H34O6/c1-15-10-18-11-19-21-13-30(34)12-17-6-9-24(32)36-28(3,4)20(17)7-8-23(30)29(21,5)14-22(31)25(19)16(2)26(18)35-27(15)33/h6,9-12,20-23,31,34H,7-8,13-14H2,1-5H3/t20-,21+,22-,23+,29-,30-/m1/s1
InChI Key DMOCICSLTAAKOU-VBLYNVHQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H34O6
Molecular Weight 490.60 g/mol
Exact Mass 490.23553880 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 3.70
Atomic LogP (AlogP) 4.92
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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1100747-35-0
KadcoccilactoneL

2D Structure

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2D Structure of Kadcoccilactone L

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9859 98.59%
Caco-2 - 0.6275 62.75%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8349 83.49%
OATP2B1 inhibitior - 0.7075 70.75%
OATP1B1 inhibitior + 0.8864 88.64%
OATP1B3 inhibitior + 0.8295 82.95%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6821 68.21%
BSEP inhibitior + 0.9709 97.09%
P-glycoprotein inhibitior + 0.7552 75.52%
P-glycoprotein substrate + 0.5378 53.78%
CYP3A4 substrate + 0.6923 69.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8722 87.22%
CYP3A4 inhibition - 0.7623 76.23%
CYP2C9 inhibition - 0.7195 71.95%
CYP2C19 inhibition - 0.8085 80.85%
CYP2D6 inhibition - 0.9070 90.70%
CYP1A2 inhibition - 0.5425 54.25%
CYP2C8 inhibition + 0.6571 65.71%
CYP inhibitory promiscuity - 0.8875 88.75%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5608 56.08%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.9430 94.30%
Skin irritation - 0.6226 62.26%
Skin corrosion - 0.9304 93.04%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7171 71.71%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.7937 79.37%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.7461 74.61%
Acute Oral Toxicity (c) III 0.3964 39.64%
Estrogen receptor binding + 0.8947 89.47%
Androgen receptor binding + 0.7290 72.90%
Thyroid receptor binding + 0.6403 64.03%
Glucocorticoid receptor binding + 0.8780 87.80%
Aromatase binding + 0.7183 71.83%
PPAR gamma + 0.6789 67.89%
Honey bee toxicity - 0.8373 83.73%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5700 57.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.64% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.24% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.19% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.87% 92.94%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.19% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.99% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.95% 94.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.87% 100.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.56% 93.00%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 84.08% 85.49%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.43% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.18% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.99% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.80% 96.77%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.60% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.15% 86.33%

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.
Kadsura coccinea

Cross-Links

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PubChem 25180593
LOTUS LTS0242785
wikiData Q104985238