Sinensol D

Details

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Internal ID ec68d3de-fd95-4b0a-afb2-80681a3a3fee
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name 7-[(4-hydroxyphenyl)methyl]-8-methoxy-2,2-dimethyl-5,6-dihydronaphtho[2,1-f]chromen-10-ol
SMILES (Canonical) CC1(C=CC2=C(O1)C=CC3=C2CCC4=C3C(=CC(=C4CC5=CC=C(C=C5)O)OC)O)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C=CC3=C2CCC4=C3C(=CC(=C4CC5=CC=C(C=C5)O)OC)O)C
InChI InChI=1S/C27H26O4/c1-27(2)13-12-19-18-8-9-21-22(14-16-4-6-17(28)7-5-16)25(30-3)15-23(29)26(21)20(18)10-11-24(19)31-27/h4-7,10-13,15,28-29H,8-9,14H2,1-3H3
InChI Key OBAJVJGJCGPZCJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C27H26O4
Molecular Weight 414.50 g/mol
Exact Mass 414.18310931 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 5.90
Atomic LogP (AlogP) 5.65
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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CHEMBL471472

2D Structure

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2D Structure of Sinensol D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9357 93.57%
Caco-2 - 0.5125 51.25%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8169 81.69%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.7519 75.19%
OATP1B3 inhibitior + 0.9494 94.94%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.9941 99.41%
P-glycoprotein inhibitior + 0.8369 83.69%
P-glycoprotein substrate + 0.5393 53.93%
CYP3A4 substrate + 0.6600 66.00%
CYP2C9 substrate + 0.5981 59.81%
CYP2D6 substrate + 0.4032 40.32%
CYP3A4 inhibition - 0.7345 73.45%
CYP2C9 inhibition - 0.6146 61.46%
CYP2C19 inhibition + 0.6169 61.69%
CYP2D6 inhibition - 0.7826 78.26%
CYP1A2 inhibition + 0.6265 62.65%
CYP2C8 inhibition + 0.8478 84.78%
CYP inhibitory promiscuity + 0.7137 71.37%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6992 69.92%
Eye corrosion - 0.9885 98.85%
Eye irritation - 0.7600 76.00%
Skin irritation - 0.8146 81.46%
Skin corrosion - 0.9568 95.68%
Ames mutagenesis - 0.5337 53.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7749 77.49%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5301 53.01%
skin sensitisation - 0.8520 85.20%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6553 65.53%
Acute Oral Toxicity (c) III 0.5115 51.15%
Estrogen receptor binding + 0.9385 93.85%
Androgen receptor binding + 0.7996 79.96%
Thyroid receptor binding + 0.7864 78.64%
Glucocorticoid receptor binding + 0.9183 91.83%
Aromatase binding + 0.6813 68.13%
PPAR gamma + 0.8660 86.60%
Honey bee toxicity - 0.7614 76.14%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.5951 59.51%
Fish aquatic toxicity + 0.9855 98.55%

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 99.30% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.94% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.87% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.43% 94.45%
CHEMBL4208 P20618 Proteasome component C5 93.93% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.84% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.59% 95.89%
CHEMBL242 Q92731 Estrogen receptor beta 91.54% 98.35%
CHEMBL2535 P11166 Glucose transporter 91.22% 98.75%
CHEMBL1951 P21397 Monoamine oxidase A 90.74% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.35% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.53% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.58% 93.99%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 87.21% 95.78%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.79% 95.56%
CHEMBL1255126 O15151 Protein Mdm4 86.68% 90.20%
CHEMBL5747 Q92793 CREB-binding protein 86.15% 95.12%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.90% 95.50%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 84.90% 95.34%
CHEMBL5555 O00767 Acyl-CoA desaturase 84.79% 97.50%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 84.51% 95.53%
CHEMBL2413 P32246 C-C chemokine receptor type 1 84.41% 89.50%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.40% 93.40%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.09% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.42% 99.15%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.29% 95.17%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.13% 97.14%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 82.29% 85.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.78% 92.62%
CHEMBL6175 Q9H3R0 Lysine-specific demethylase 4C 80.82% 96.69%

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.
Spiranthes sinensis
Spiranthes vernalis

Cross-Links

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PubChem 10621720
LOTUS LTS0153061
wikiData Q105188917