Details

Top
Internal ID 5407b622-e4f0-4b9f-b1ee-08b1a7e4ef09
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C56H38O12/c57-29-9-1-25(2-10-29)45-47-37(17-33(61)21-41(47)65)53-49-39(19-35(63)23-43(49)67-55(53)27-5-13-31(59)14-6-27)51(45)52-40-20-36(64)24-44-50(40)54(56(68-44)28-7-15-32(60)16-8-28)38-18-34(62)22-42(66)48(38)46(52)26-3-11-30(58)12-4-26/h1-24,45,51-53,55,57,59-66H/t45-,51-,52-,53-,55+/m1/s1
InChI Key SEMLMSKWBGDESX-ZDOZYXMHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C56H38O12
Molecular Weight 902.90 g/mol
Exact Mass 902.23632664 g/mol
Topological Polar Surface Area (TPSA) 222.00 Ų
XlogP 8.80
Atomic LogP (AlogP) 10.86
H-Bond Acceptor 12
H-Bond Donor 9
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 - 0.8984 89.84%
Blood Brain Barrier - 0.6629 66.29%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6654 66.54%
OATP2B1 inhibitior + 0.5817 58.17%
OATP1B1 inhibitior + 0.7965 79.65%
OATP1B3 inhibitior + 0.8221 82.21%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.8785 87.85%
P-glycoprotein inhibitior + 0.7168 71.68%
P-glycoprotein substrate + 0.5410 54.10%
CYP3A4 substrate + 0.6938 69.38%
CYP2C9 substrate - 0.7905 79.05%
CYP2D6 substrate - 0.7998 79.98%
CYP3A4 inhibition + 0.7831 78.31%
CYP2C9 inhibition + 0.8921 89.21%
CYP2C19 inhibition + 0.8461 84.61%
CYP2D6 inhibition - 0.8766 87.66%
CYP1A2 inhibition + 0.8571 85.71%
CYP2C8 inhibition + 0.8878 88.78%
CYP inhibitory promiscuity + 0.9678 96.78%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4251 42.51%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.8446 84.46%
Skin irritation - 0.5666 56.66%
Skin corrosion - 0.9463 94.63%
Ames mutagenesis - 0.5264 52.64%
Human Ether-a-go-go-Related Gene inhibition + 0.7938 79.38%
Micronuclear + 0.9300 93.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.6827 68.27%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.6326 63.26%
Acute Oral Toxicity (c) II 0.4081 40.81%
Estrogen receptor binding + 0.8246 82.46%
Androgen receptor binding + 0.8206 82.06%
Thyroid receptor binding + 0.6002 60.02%
Glucocorticoid receptor binding + 0.6681 66.81%
Aromatase binding - 0.5846 58.46%
PPAR gamma + 0.7178 71.78%
Honey bee toxicity - 0.7108 71.08%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9915 99.15%

Targets

Top

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 98.56% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.62% 89.00%
CHEMBL2581 P07339 Cathepsin D 96.26% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.14% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.01% 99.23%
CHEMBL1929 P47989 Xanthine dehydrogenase 90.75% 96.12%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.62% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.41% 85.14%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 89.26% 95.78%
CHEMBL242 Q92731 Estrogen receptor beta 88.96% 98.35%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.71% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.85% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.52% 93.40%
CHEMBL3194 P02766 Transthyretin 83.99% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 83.87% 94.73%
CHEMBL4530 P00488 Coagulation factor XIII 82.88% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.80% 86.33%
CHEMBL4208 P20618 Proteasome component C5 80.99% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.48% 99.17%

Plants that contains it

Top
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.
Upuna borneensis

Cross-Links

Top
PubChem 16154774
LOTUS LTS0050178
wikiData Q105251285