Scortechinone W

Details

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Internal ID 4928cb53-dd90-47e8-a04d-d2e2e54ae6e8
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name (7S)-7-[(E)-3-carboxybut-2-enyl]-14-hydroxy-9-methoxy-5,5,16,16,17-pentamethyl-20-(3-methylbut-2-enyl)-12-oxo-2,6,18-trioxapentacyclo[11.7.0.03,11.04,8.015,19]icosa-1(20),3,8,10,13,15(19)-hexaene-7-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C34H38O10/c1-15(2)10-11-18-27-21(26(36)24-28(18)42-17(4)32(24,5)6)25(35)19-14-20(41-9)22-23(29(19)43-27)33(7,8)44-34(22,31(39)40)13-12-16(3)30(37)38/h10,12,14,17,36H,11,13H2,1-9H3,(H,37,38)(H,39,40)/b16-12+/t17?,34-/m0/s1
InChI Key FZCGEJLHEWDOTR-SJDNDDLKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C34H38O10
Molecular Weight 606.70 g/mol
Exact Mass 606.24649740 g/mol
Topological Polar Surface Area (TPSA) 149.00 Ų
XlogP 6.50
Atomic LogP (AlogP) 6.19
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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CHEMBL510785

2D Structure

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2D Structure of Scortechinone W

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9724 97.24%
Caco-2 - 0.7783 77.83%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6777 67.77%
OATP2B1 inhibitior - 0.8574 85.74%
OATP1B1 inhibitior + 0.7988 79.88%
OATP1B3 inhibitior - 0.3517 35.17%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9792 97.92%
P-glycoprotein inhibitior + 0.7586 75.86%
P-glycoprotein substrate + 0.6084 60.84%
CYP3A4 substrate + 0.6754 67.54%
CYP2C9 substrate + 0.6198 61.98%
CYP2D6 substrate - 0.8827 88.27%
CYP3A4 inhibition - 0.7515 75.15%
CYP2C9 inhibition + 0.5600 56.00%
CYP2C19 inhibition - 0.5335 53.35%
CYP2D6 inhibition - 0.8116 81.16%
CYP1A2 inhibition - 0.6198 61.98%
CYP2C8 inhibition + 0.6903 69.03%
CYP inhibitory promiscuity + 0.5749 57.49%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Danger 0.4599 45.99%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.8732 87.32%
Skin irritation - 0.7449 74.49%
Skin corrosion - 0.9309 93.09%
Ames mutagenesis + 0.5635 56.35%
Human Ether-a-go-go-Related Gene inhibition - 0.5130 51.30%
Micronuclear - 0.5200 52.00%
Hepatotoxicity - 0.6073 60.73%
skin sensitisation - 0.7825 78.25%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.8117 81.17%
Acute Oral Toxicity (c) I 0.4349 43.49%
Estrogen receptor binding + 0.7503 75.03%
Androgen receptor binding + 0.7181 71.81%
Thyroid receptor binding + 0.5814 58.14%
Glucocorticoid receptor binding + 0.7552 75.52%
Aromatase binding + 0.7799 77.99%
PPAR gamma + 0.7312 73.12%
Honey bee toxicity - 0.7523 75.23%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9907 99.07%

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 99.43% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.56% 89.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 95.99% 92.94%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.50% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.45% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.85% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.57% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.12% 95.56%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 92.17% 85.30%
CHEMBL340 P08684 Cytochrome P450 3A4 91.57% 91.19%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.35% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.75% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.50% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 87.86% 90.20%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.63% 94.42%
CHEMBL1937 Q92769 Histone deacetylase 2 87.48% 94.75%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 84.77% 92.38%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 84.58% 82.38%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.57% 89.34%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.35% 95.89%
CHEMBL2535 P11166 Glucose transporter 82.57% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 82.41% 94.73%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.29% 91.07%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.75% 89.50%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.35% 96.09%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.76% 94.03%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.07% 95.50%

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.
Garcinia scortechinii

Cross-Links

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PubChem 11678846
LOTUS LTS0036634
wikiData Q105004855