saucerneol D

Details

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Internal ID aee7f1ab-df98-4a40-84d6-e18a059170e1
Taxonomy Lignans, neolignans and related compounds > Furanoid lignans > Tetrahydrofuran lignans > 7,7-epoxylignans
IUPAC Name (1S,2R)-2-[4-[(2S,3R,4R,5S)-5-(1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenoxy]-1-(3,4-dimethoxyphenyl)propan-1-ol
SMILES (Canonical) CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC(C)C(C5=CC(=C(C=C5)OC)OC)O)OC)C
SMILES (Isomeric) C[C@@H]1[C@H]([C@H](O[C@@H]1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O[C@H](C)[C@H](C5=CC(=C(C=C5)OC)OC)O)OC)C
InChI InChI=1S/C31H36O8/c1-17-18(2)31(22-8-11-24-28(15-22)37-16-36-24)39-30(17)21-9-12-25(27(14-21)35-6)38-19(3)29(32)20-7-10-23(33-4)26(13-20)34-5/h7-15,17-19,29-32H,16H2,1-6H3/t17-,18-,19-,29-,30+,31+/m1/s1
InChI Key BYTPMMJRDFCGKX-GJRFZWDISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H36O8
Molecular Weight 536.60 g/mol
Exact Mass 536.24101810 g/mol
Topological Polar Surface Area (TPSA) 84.80 Ų
XlogP 5.50
Atomic LogP (AlogP) 6.03
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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CHEMBL520077

2D Structure

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2D Structure of saucerneol D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 - 0.6558 65.58%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7681 76.81%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.9003 90.03%
OATP1B3 inhibitior + 0.9160 91.60%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9608 96.08%
P-glycoprotein inhibitior + 0.8861 88.61%
P-glycoprotein substrate - 0.6548 65.48%
CYP3A4 substrate + 0.5449 54.49%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6666 66.66%
CYP3A4 inhibition + 0.8155 81.55%
CYP2C9 inhibition + 0.9215 92.15%
CYP2C19 inhibition + 0.8696 86.96%
CYP2D6 inhibition + 0.5354 53.54%
CYP1A2 inhibition + 0.6001 60.01%
CYP2C8 inhibition - 0.8292 82.92%
CYP inhibitory promiscuity + 0.8927 89.27%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9308 93.08%
Carcinogenicity (trinary) Warning 0.3491 34.91%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9150 91.50%
Skin irritation - 0.7866 78.66%
Skin corrosion - 0.9715 97.15%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7678 76.78%
Micronuclear + 0.7600 76.00%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.8185 81.85%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6447 64.47%
Acute Oral Toxicity (c) III 0.6252 62.52%
Estrogen receptor binding + 0.8364 83.64%
Androgen receptor binding + 0.6393 63.93%
Thyroid receptor binding + 0.6693 66.93%
Glucocorticoid receptor binding + 0.7596 75.96%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.7473 74.73%
Honey bee toxicity - 0.7870 78.70%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9518 95.18%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.33% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.03% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.33% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.69% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.42% 94.45%
CHEMBL4208 P20618 Proteasome component C5 91.21% 90.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 89.73% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.70% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.57% 97.09%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.20% 89.62%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.40% 97.14%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.11% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.74% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.63% 94.80%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 87.24% 96.86%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 86.95% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.38% 92.62%
CHEMBL2413 P32246 C-C chemokine receptor type 1 85.60% 89.50%
CHEMBL2535 P11166 Glucose transporter 85.52% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.21% 95.89%
CHEMBL3438 Q05513 Protein kinase C zeta 83.01% 88.48%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 82.61% 82.67%
CHEMBL3401 O75469 Pregnane X receptor 82.60% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.01% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.55% 96.00%

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.
Juniperus communis
Pinus sibirica
Pteris multifida
Saururus chinensis

Cross-Links

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PubChem 44580018
NPASS NPC302506
ChEMBL CHEMBL520077
LOTUS LTS0212954
wikiData Q105378970