(17S)-12,21,22-trihydroxy-8,8,18,18-tetramethyl-3,9,19-trioxahexacyclo[15.6.1.02,15.04,13.05,10.020,24]tetracosa-1(23),2(15),4(13),5(10),6,11,20(24),21-octaen-14-one

Details

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Internal ID a6914e78-908a-46f6-a74a-dd2a067a9913
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > Pyranoxanthones
IUPAC Name (17S)-12,21,22-trihydroxy-8,8,18,18-tetramethyl-3,9,19-trioxahexacyclo[15.6.1.02,15.04,13.05,10.020,24]tetracosa-1(23),2(15),4(13),5(10),6,11,20(24),21-octaen-14-one
SMILES (Canonical) CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)CC5C6=C(C(=C(C=C64)O)O)OC5(C)C)O)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C[C@H]5C6=C(C(=C(C=C64)O)O)OC5(C)C)O)C
InChI InChI=1S/C25H22O7/c1-24(2)6-5-10-16(31-24)9-14(26)18-19(28)12-7-13-17-11(21(12)30-22(10)18)8-15(27)20(29)23(17)32-25(13,3)4/h5-6,8-9,13,26-27,29H,7H2,1-4H3/t13-/m0/s1
InChI Key FNUANQPCXYWIED-ZDUSSCGKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C25H22O7
Molecular Weight 434.40 g/mol
Exact Mass 434.13655304 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.57
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (17S)-12,21,22-trihydroxy-8,8,18,18-tetramethyl-3,9,19-trioxahexacyclo[15.6.1.02,15.04,13.05,10.020,24]tetracosa-1(23),2(15),4(13),5(10),6,11,20(24),21-octaen-14-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 - 0.6239 62.39%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7509 75.09%
OATP2B1 inhibitior - 0.7099 70.99%
OATP1B1 inhibitior + 0.8575 85.75%
OATP1B3 inhibitior + 0.9763 97.63%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.5964 59.64%
P-glycoprotein inhibitior + 0.6315 63.15%
P-glycoprotein substrate + 0.5711 57.11%
CYP3A4 substrate + 0.6562 65.62%
CYP2C9 substrate - 0.5919 59.19%
CYP2D6 substrate - 0.8252 82.52%
CYP3A4 inhibition - 0.7690 76.90%
CYP2C9 inhibition - 0.6313 63.13%
CYP2C19 inhibition - 0.5275 52.75%
CYP2D6 inhibition - 0.8046 80.46%
CYP1A2 inhibition + 0.6842 68.42%
CYP2C8 inhibition + 0.5688 56.88%
CYP inhibitory promiscuity + 0.5127 51.27%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4485 44.85%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.5442 54.42%
Skin irritation - 0.6652 66.52%
Skin corrosion - 0.8995 89.95%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5316 53.16%
Micronuclear + 0.5800 58.00%
Hepatotoxicity - 0.6199 61.99%
skin sensitisation - 0.6945 69.45%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7201 72.01%
Acute Oral Toxicity (c) III 0.6071 60.71%
Estrogen receptor binding + 0.8915 89.15%
Androgen receptor binding + 0.7893 78.93%
Thyroid receptor binding + 0.6549 65.49%
Glucocorticoid receptor binding + 0.8327 83.27%
Aromatase binding + 0.6030 60.30%
PPAR gamma + 0.7583 75.83%
Honey bee toxicity - 0.7954 79.54%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9903 99.03%

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 99.81% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.62% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 95.59% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.37% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.97% 94.45%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 91.49% 85.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.35% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.13% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.73% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.07% 94.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.05% 94.42%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.36% 96.77%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 86.02% 95.71%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.87% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.67% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.74% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.51% 90.71%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.39% 93.04%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.50% 93.40%

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.
Artocarpus kemando

Cross-Links

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PubChem 162881751
LOTUS LTS0012941
wikiData Q104998518