Isokibdelone A

Details

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Internal ID 4eb545f8-f4fb-4be5-a976-7e344493aa28
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name (5S,7S,8R)-20-chloro-5,7,8,12-tetrahydroxy-13-methoxy-22-methyl-21-propyl-3-oxa-22-azahexacyclo[12.12.0.02,11.04,9.017,26.019,24]hexacosa-1(14),2(11),4(9),12,15,17(26),19(24),20-octaene-10,18,23,25-tetrone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H24ClNO10/c1-4-5-11-20(30)16-17(29(39)31(11)2)23(36)14-9(21(16)34)6-7-10-15(14)28-19(25(38)26(10)40-3)24(37)18-22(35)12(32)8-13(33)27(18)41-28/h6-7,12-13,22,32-33,35,38H,4-5,8H2,1-3H3/t12-,13-,22-/m0/s1
InChI Key DKKCYFNZVNYTLD-MZFXBISCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C29H24ClNO10
Molecular Weight 582.00 g/mol
Exact Mass 581.1088737 g/mol
Topological Polar Surface Area (TPSA) 171.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.57
H-Bond Acceptor 11
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Isokibdelone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8845 88.45%
Caco-2 - 0.8409 84.09%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.3666 36.66%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.8299 82.99%
OATP1B3 inhibitior + 0.9238 92.38%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.7822 78.22%
BSEP inhibitior + 0.7408 74.08%
P-glycoprotein inhibitior + 0.5853 58.53%
P-glycoprotein substrate + 0.7966 79.66%
CYP3A4 substrate + 0.7253 72.53%
CYP2C9 substrate + 0.7984 79.84%
CYP2D6 substrate - 0.8498 84.98%
CYP3A4 inhibition - 0.7135 71.35%
CYP2C9 inhibition - 0.7848 78.48%
CYP2C19 inhibition - 0.7642 76.42%
CYP2D6 inhibition - 0.8756 87.56%
CYP1A2 inhibition - 0.6641 66.41%
CYP2C8 inhibition + 0.7048 70.48%
CYP inhibitory promiscuity - 0.7774 77.74%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.4537 45.37%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.9455 94.55%
Skin irritation - 0.7922 79.22%
Skin corrosion - 0.9302 93.02%
Ames mutagenesis + 0.5992 59.92%
Human Ether-a-go-go-Related Gene inhibition - 0.4770 47.70%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.5751 57.51%
skin sensitisation - 0.8677 86.77%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.8175 81.75%
Acute Oral Toxicity (c) III 0.6025 60.25%
Estrogen receptor binding + 0.8178 81.78%
Androgen receptor binding + 0.6534 65.34%
Thyroid receptor binding + 0.5553 55.53%
Glucocorticoid receptor binding + 0.7681 76.81%
Aromatase binding + 0.6745 67.45%
PPAR gamma + 0.6904 69.04%
Honey bee toxicity - 0.7420 74.20%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.7860 78.60%

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
CHEMBL2581 P07339 Cathepsin D 99.01% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.41% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.35% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.84% 89.00%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 94.83% 95.34%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.45% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.46% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.09% 96.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.56% 86.92%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.17% 95.89%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.32% 85.94%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.93% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.93% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 87.09% 91.49%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.68% 90.71%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 86.20% 95.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.74% 92.62%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.26% 96.95%
CHEMBL226 P30542 Adenosine A1 receptor 84.93% 95.93%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.75% 96.77%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 84.75% 98.46%
CHEMBL255 P29275 Adenosine A2b receptor 84.05% 98.59%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.54% 94.42%
CHEMBL1871 P10275 Androgen Receptor 83.30% 96.43%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.32% 100.00%
CHEMBL3820 P35557 Hexokinase type IV 81.21% 91.96%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.93% 96.67%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.01% 97.14%

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 11994733
LOTUS LTS0066753
wikiData Q77421517