Globuxanthone

Details

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Internal ID a95e7e65-925b-4c3b-ad1a-6a940abec6d3
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,2,5-trihydroxy-4-(2-methylbut-3-en-2-yl)xanthen-9-one
SMILES (Canonical) CC(C)(C=C)C1=CC(=C(C2=C1OC3=C(C2=O)C=CC=C3O)O)O
SMILES (Isomeric) CC(C)(C=C)C1=CC(=C(C2=C1OC3=C(C2=O)C=CC=C3O)O)O
InChI InChI=1S/C18H16O5/c1-4-18(2,3)10-8-12(20)15(22)13-14(21)9-6-5-7-11(19)16(9)23-17(10)13/h4-8,19-20,22H,1H2,2-3H3
InChI Key OBZOCMORJAPERH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O5
Molecular Weight 312.30 g/mol
Exact Mass 312.09977361 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.53
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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BDBM50268297

2D Structure

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2D Structure of Globuxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9694 96.94%
Caco-2 - 0.5573 55.73%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7284 72.84%
OATP2B1 inhibitior - 0.6966 69.66%
OATP1B1 inhibitior + 0.8998 89.98%
OATP1B3 inhibitior + 0.9888 98.88%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5101 51.01%
P-glycoprotein inhibitior - 0.6655 66.55%
P-glycoprotein substrate - 0.7927 79.27%
CYP3A4 substrate + 0.5603 56.03%
CYP2C9 substrate - 0.6339 63.39%
CYP2D6 substrate - 0.8641 86.41%
CYP3A4 inhibition + 0.5751 57.51%
CYP2C9 inhibition - 0.5500 55.00%
CYP2C19 inhibition - 0.5439 54.39%
CYP2D6 inhibition - 0.8129 81.29%
CYP1A2 inhibition + 0.7584 75.84%
CYP2C8 inhibition + 0.5278 52.78%
CYP inhibitory promiscuity - 0.5813 58.13%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6207 62.07%
Eye corrosion - 0.9864 98.64%
Eye irritation + 0.8491 84.91%
Skin irritation - 0.6491 64.91%
Skin corrosion - 0.8154 81.54%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6082 60.82%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.6215 62.15%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6673 66.73%
Acute Oral Toxicity (c) III 0.6502 65.02%
Estrogen receptor binding + 0.8359 83.59%
Androgen receptor binding + 0.7167 71.67%
Thyroid receptor binding + 0.6497 64.97%
Glucocorticoid receptor binding + 0.9038 90.38%
Aromatase binding + 0.8030 80.30%
PPAR gamma + 0.8315 83.15%
Honey bee toxicity - 0.9048 90.48%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9904 99.04%

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 98.79% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.79% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 96.72% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.38% 89.00%
CHEMBL2581 P07339 Cathepsin D 93.98% 98.95%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 92.60% 83.57%
CHEMBL1951 P21397 Monoamine oxidase A 91.26% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.16% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.93% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.24% 99.23%
CHEMBL4530 P00488 Coagulation factor XIII 87.37% 96.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.14% 93.99%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.64% 93.65%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.17% 89.34%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 80.66% 98.11%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.50% 80.78%

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 subelliptica
Garcinia vilersiana
Garcinia xanthochymus
Symphonia globulifera

Cross-Links

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PubChem 60148490
NPASS NPC109713
LOTUS LTS0274253
wikiData Q104397990