Sequosempervirin F

Details

Top
Internal ID 01b03b3b-4c32-481c-a9f0-ef839c01e75b
Taxonomy Lignans, neolignans and related compounds
IUPAC Name (3S,4S,6R)-4-(4-hydroxy-3-methoxyphenyl)-6-(4-hydroxyphenyl)oxan-3-ol
SMILES (Canonical) COC1=C(C=CC(=C1)C2CC(OCC2O)C3=CC=C(C=C3)O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)[C@@H]2C[C@@H](OC[C@H]2O)C3=CC=C(C=C3)O)O
InChI InChI=1S/C18H20O5/c1-22-18-8-12(4-7-15(18)20)14-9-17(23-10-16(14)21)11-2-5-13(19)6-3-11/h2-8,14,16-17,19-21H,9-10H2,1H3/t14-,16+,17+/m0/s1
InChI Key OSCHVWVCQJBFNN-USXIJHARSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C18H20O5
Molecular Weight 316.30 g/mol
Exact Mass 316.13107373 g/mol
Topological Polar Surface Area (TPSA) 79.20 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.71
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

Top
CHEBI:69977
Q27138322

2D Structure

Top
2D Structure of Sequosempervirin F

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9578 95.78%
Caco-2 + 0.6529 65.29%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.8857 88.57%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.8863 88.63%
OATP1B3 inhibitior + 0.9064 90.64%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8873 88.73%
P-glycoprotein inhibitior - 0.7585 75.85%
P-glycoprotein substrate - 0.7926 79.26%
CYP3A4 substrate + 0.5627 56.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4750 47.50%
CYP3A4 inhibition - 0.9000 90.00%
CYP2C9 inhibition - 0.7271 72.71%
CYP2C19 inhibition - 0.5561 55.61%
CYP2D6 inhibition - 0.9100 91.00%
CYP1A2 inhibition - 0.7655 76.55%
CYP2C8 inhibition + 0.7347 73.47%
CYP inhibitory promiscuity - 0.5583 55.83%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8907 89.07%
Carcinogenicity (trinary) Non-required 0.5849 58.49%
Eye corrosion - 0.9867 98.67%
Eye irritation - 0.7674 76.74%
Skin irritation - 0.7983 79.83%
Skin corrosion - 0.9585 95.85%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5059 50.59%
Micronuclear + 0.6418 64.18%
Hepatotoxicity - 0.6820 68.20%
skin sensitisation - 0.8849 88.49%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.8306 83.06%
Acute Oral Toxicity (c) III 0.7514 75.14%
Estrogen receptor binding + 0.6051 60.51%
Androgen receptor binding + 0.5316 53.16%
Thyroid receptor binding + 0.6474 64.74%
Glucocorticoid receptor binding - 0.4854 48.54%
Aromatase binding - 0.6926 69.26%
PPAR gamma - 0.5382 53.82%
Honey bee toxicity - 0.8561 85.61%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.7608 76.08%

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 99.12% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.16% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.03% 97.09%
CHEMBL3438 Q05513 Protein kinase C zeta 92.51% 88.48%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 92.06% 89.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.23% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.23% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.94% 95.56%
CHEMBL4208 P20618 Proteasome component C5 86.75% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.92% 94.00%
CHEMBL3194 P02766 Transthyretin 83.84% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.63% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.09% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.06% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.21% 99.15%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.73% 95.89%
CHEMBL2581 P07339 Cathepsin D 81.63% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.51% 99.17%
CHEMBL301 P24941 Cyclin-dependent kinase 2 80.89% 91.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.84% 94.45%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.28% 93.10%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.15% 100.00%

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.
Metasequoia glyptostroboides

Cross-Links

Top
PubChem 70698264
NPASS NPC86927
LOTUS LTS0115313
wikiData Q27138322