Castacrenin C

Details

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Internal ID a73c8f47-11d2-4c82-bd20-649c0226e70c
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name 6,7,13,14-tetrahydroxy-5-[5,6,7-trihydroxy-1-oxo-3-(1,2,3,4-tetrahydroxybutyl)isochromen-8-yl]-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione
SMILES (Canonical) C1=C2C3=C(C(=C1O)O)OC(=O)C4=C3C(=C(C(=C4C5=C(C(=C(C6=C5C(=O)OC(=C6)C(C(C(CO)O)O)O)O)O)O)O)O)OC2=O
SMILES (Isomeric) C1=C2C3=C(C(=C1O)O)OC(=O)C4=C3C(=C(C(=C4C5=C(C(=C(C6=C5C(=O)OC(=C6)C(C(C(CO)O)O)O)O)O)O)O)O)OC2=O
InChI InChI=1S/C27H18O17/c28-3-7(30)16(32)18(34)8-2-4-10(26(40)42-8)11(19(35)21(37)15(4)31)12-14-13-9-5(25(39)43-24(13)22(38)20(12)36)1-6(29)17(33)23(9)44-27(14)41/h1-2,7,16,18,28-38H,3H2
InChI Key AQPVDJOZILVCEZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C27H18O17
Molecular Weight 614.40 g/mol
Exact Mass 614.05439910 g/mol
Topological Polar Surface Area (TPSA) 301.00 Ų
XlogP -1.10
Atomic LogP (AlogP) -0.05
H-Bond Acceptor 17
H-Bond Donor 11
Rotatable Bonds 5

Synonyms

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DTXSID601317597
173450-72-1

2D Structure

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2D Structure of Castacrenin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5363 53.63%
Caco-2 - 0.9163 91.63%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Nucleus 0.4621 46.21%
OATP2B1 inhibitior + 0.7193 71.93%
OATP1B1 inhibitior + 0.8669 86.69%
OATP1B3 inhibitior + 0.9638 96.38%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5409 54.09%
P-glycoprotein inhibitior - 0.5906 59.06%
P-glycoprotein substrate - 0.6086 60.86%
CYP3A4 substrate + 0.5427 54.27%
CYP2C9 substrate - 0.6129 61.29%
CYP2D6 substrate - 0.8519 85.19%
CYP3A4 inhibition - 0.9237 92.37%
CYP2C9 inhibition - 0.9630 96.30%
CYP2C19 inhibition - 0.9713 97.13%
CYP2D6 inhibition - 0.9609 96.09%
CYP1A2 inhibition - 0.9639 96.39%
CYP2C8 inhibition - 0.5671 56.71%
CYP inhibitory promiscuity - 0.9699 96.99%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7332 73.32%
Eye corrosion - 0.9941 99.41%
Eye irritation - 0.8622 86.22%
Skin irritation - 0.8046 80.46%
Skin corrosion - 0.9577 95.77%
Ames mutagenesis - 0.5464 54.64%
Human Ether-a-go-go-Related Gene inhibition + 0.7788 77.88%
Micronuclear + 0.6733 67.33%
Hepatotoxicity - 0.7198 71.98%
skin sensitisation - 0.8991 89.91%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.9218 92.18%
Acute Oral Toxicity (c) IV 0.3818 38.18%
Estrogen receptor binding + 0.7573 75.73%
Androgen receptor binding + 0.7182 71.82%
Thyroid receptor binding + 0.5164 51.64%
Glucocorticoid receptor binding + 0.6936 69.36%
Aromatase binding + 0.5279 52.79%
PPAR gamma + 0.7732 77.32%
Honey bee toxicity - 0.8669 86.69%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.7966 79.66%

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 99.05% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.17% 94.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 92.64% 89.34%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.14% 89.00%
CHEMBL2581 P07339 Cathepsin D 91.90% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.90% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.66% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.61% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 86.18% 94.73%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.28% 96.67%
CHEMBL301 P24941 Cyclin-dependent kinase 2 82.38% 91.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.79% 99.17%
CHEMBL3194 P02766 Transthyretin 81.07% 90.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.26% 90.71%

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.
Castanea crenata

Cross-Links

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PubChem 85228592
LOTUS LTS0264072
wikiData Q104916992