(8S,9R,10S)-3,4,5,19-tetramethoxy-9,10-dimethyl-8-phenoxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-9-ol

Details

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Internal ID 864d040d-5f09-4a22-85d4-0c037a2a07f8
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name (8S,9R,10S)-3,4,5,19-tetramethoxy-9,10-dimethyl-8-phenoxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-9-ol
SMILES (Canonical) CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC5=CC=CC=C5)OC)OC)OC)OC)OCO3
SMILES (Isomeric) C[C@H]1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4[C@@H]([C@]1(C)O)OC5=CC=CC=C5)OC)OC)OC)OC)OCO3
InChI InChI=1S/C29H32O8/c1-16-12-17-13-21-25(36-15-35-21)26(33-5)22(17)23-19(14-20(31-3)24(32-4)27(23)34-6)28(29(16,2)30)37-18-10-8-7-9-11-18/h7-11,13-14,16,28,30H,12,15H2,1-6H3/t16-,28-,29+/m0/s1
InChI Key MSHJHBLTCDLVSX-MQUUAHRSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H32O8
Molecular Weight 508.60 g/mol
Exact Mass 508.20971797 g/mol
Topological Polar Surface Area (TPSA) 84.80 Ų
XlogP 5.10
Atomic LogP (AlogP) 5.18
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8S,9R,10S)-3,4,5,19-tetramethoxy-9,10-dimethyl-8-phenoxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-9-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9868 98.68%
Caco-2 + 0.7085 70.85%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.5886 58.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9022 90.22%
OATP1B3 inhibitior + 0.9331 93.31%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9554 95.54%
P-glycoprotein inhibitior + 0.9099 90.99%
P-glycoprotein substrate - 0.7012 70.12%
CYP3A4 substrate + 0.6620 66.20%
CYP2C9 substrate - 0.5852 58.52%
CYP2D6 substrate + 0.3508 35.08%
CYP3A4 inhibition + 0.7409 74.09%
CYP2C9 inhibition + 0.5972 59.72%
CYP2C19 inhibition + 0.5355 53.55%
CYP2D6 inhibition - 0.7233 72.33%
CYP1A2 inhibition - 0.6045 60.45%
CYP2C8 inhibition + 0.7020 70.20%
CYP inhibitory promiscuity - 0.5239 52.39%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4266 42.66%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9064 90.64%
Skin irritation - 0.7812 78.12%
Skin corrosion - 0.9528 95.28%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8252 82.52%
Micronuclear + 0.5500 55.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.7888 78.88%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.8059 80.59%
Acute Oral Toxicity (c) III 0.5910 59.10%
Estrogen receptor binding + 0.8645 86.45%
Androgen receptor binding + 0.5955 59.55%
Thyroid receptor binding + 0.7362 73.62%
Glucocorticoid receptor binding + 0.8010 80.10%
Aromatase binding + 0.5890 58.90%
PPAR gamma + 0.8133 81.33%
Honey bee toxicity - 0.7111 71.11%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.9815 98.15%

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 99.35% 91.11%
CHEMBL261 P00915 Carbonic anhydrase I 97.74% 96.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.79% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.52% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.66% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.41% 92.62%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 87.09% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.18% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.68% 95.89%
CHEMBL240 Q12809 HERG 85.48% 89.76%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.44% 94.45%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.11% 95.89%
CHEMBL2535 P11166 Glucose transporter 85.02% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.98% 93.99%
CHEMBL4208 P20618 Proteasome component C5 84.57% 90.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.97% 97.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.26% 99.17%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.72% 94.03%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.75% 97.09%
CHEMBL2056 P21728 Dopamine D1 receptor 81.17% 91.00%

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.
Schisandra arisanensis
Schisandra sphenanthera

Cross-Links

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PubChem 5317798
LOTUS LTS0132671
wikiData Q105171170