selaginellin J

Details

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Internal ID 01f21445-b71b-4421-a25a-460e72093365
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name 4-[[2-[2-(3,4-dihydroxyphenyl)ethynyl]-3-(hydroxymethyl)-6-(4-hydroxyphenyl)phenyl]-(4-hydroxyphenyl)methylidene]cyclohexa-2,5-dien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C34H24O6/c35-20-25-9-17-29(22-3-10-26(36)11-4-22)34(30(25)16-1-21-2-18-31(39)32(40)19-21)33(23-5-12-27(37)13-6-23)24-7-14-28(38)15-8-24/h2-15,17-19,35-37,39-40H,20H2
InChI Key BPEDBCRRNTUBDG-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C34H24O6
Molecular Weight 528.50 g/mol
Exact Mass 528.15728848 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP 5.90
Atomic LogP (AlogP) 5.57
H-Bond Acceptor 6
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of selaginellin J

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9810 98.10%
Caco-2 - 0.9177 91.77%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8444 84.44%
OATP2B1 inhibitior + 0.5758 57.58%
OATP1B1 inhibitior + 0.8802 88.02%
OATP1B3 inhibitior + 0.9119 91.19%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9308 93.08%
P-glycoprotein inhibitior - 0.5055 50.55%
P-glycoprotein substrate - 0.5691 56.91%
CYP3A4 substrate + 0.6358 63.58%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8325 83.25%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition + 0.6199 61.99%
CYP2C19 inhibition - 0.6194 61.94%
CYP2D6 inhibition - 0.8664 86.64%
CYP1A2 inhibition + 0.8327 83.27%
CYP2C8 inhibition + 0.9143 91.43%
CYP inhibitory promiscuity + 0.8315 83.15%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7223 72.23%
Carcinogenicity (trinary) Non-required 0.7009 70.09%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.7731 77.31%
Skin irritation - 0.7204 72.04%
Skin corrosion - 0.9293 92.93%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7204 72.04%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.5981 59.81%
skin sensitisation + 0.5905 59.05%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.6253 62.53%
Acute Oral Toxicity (c) III 0.5808 58.08%
Estrogen receptor binding + 0.8603 86.03%
Androgen receptor binding + 0.9129 91.29%
Thyroid receptor binding + 0.5435 54.35%
Glucocorticoid receptor binding + 0.7395 73.95%
Aromatase binding + 0.5623 56.23%
PPAR gamma + 0.8477 84.77%
Honey bee toxicity - 0.8185 81.85%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9931 99.31%

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 98.44% 91.11%
CHEMBL242 Q92731 Estrogen receptor beta 97.61% 98.35%
CHEMBL2581 P07339 Cathepsin D 93.50% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.05% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.96% 99.15%
CHEMBL4208 P20618 Proteasome component C5 90.82% 90.00%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 90.60% 93.10%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 90.06% 91.71%
CHEMBL3194 P02766 Transthyretin 89.67% 90.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.33% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.00% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.61% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.03% 86.92%
CHEMBL1929 P47989 Xanthine dehydrogenase 85.67% 96.12%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.51% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.61% 94.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.31% 90.71%
CHEMBL2535 P11166 Glucose transporter 81.96% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 81.85% 94.73%
CHEMBL206 P03372 Estrogen receptor alpha 80.87% 97.64%
CHEMBL1907 P15144 Aminopeptidase N 80.28% 93.31%

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.
Selaginella tamariscina

Cross-Links

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PubChem 123383224
LOTUS LTS0144607
wikiData Q104941958