aglacin C

Details

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Internal ID 3db6b303-2318-425c-a2ee-7eb0a3c8dba2
Taxonomy Lignans, neolignans and related compounds > Aryltetralin lignans
IUPAC Name (3aS,4R,9aS)-4-(3,4-dimethoxyphenyl)-5,6,7-trimethoxy-1,3,3a,4,9,9a-hexahydrobenzo[f][2]benzofuran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H28O6/c1-24-17-7-6-13(9-18(17)25-2)20-16-12-29-11-15(16)8-14-10-19(26-3)22(27-4)23(28-5)21(14)20/h6-7,9-10,15-16,20H,8,11-12H2,1-5H3/t15-,16-,20+/m1/s1
InChI Key RKVVUMUMIOPICX-QINHECLXSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H28O6
Molecular Weight 400.50 g/mol
Exact Mass 400.18858861 g/mol
Topological Polar Surface Area (TPSA) 55.40 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.68
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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CHEMBL491182

2D Structure

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2D Structure of aglacin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9037 90.37%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7039 70.39%
OATP2B1 inhibitior - 0.8716 87.16%
OATP1B1 inhibitior + 0.9273 92.73%
OATP1B3 inhibitior + 0.9797 97.97%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.8970 89.70%
P-glycoprotein inhibitior + 0.7935 79.35%
P-glycoprotein substrate - 0.6974 69.74%
CYP3A4 substrate + 0.5724 57.24%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate + 0.5712 57.12%
CYP3A4 inhibition + 0.6102 61.02%
CYP2C9 inhibition + 0.7415 74.15%
CYP2C19 inhibition + 0.8310 83.10%
CYP2D6 inhibition - 0.8637 86.37%
CYP1A2 inhibition + 0.6666 66.66%
CYP2C8 inhibition + 0.6128 61.28%
CYP inhibitory promiscuity + 0.8903 89.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9108 91.08%
Carcinogenicity (trinary) Non-required 0.4940 49.40%
Eye corrosion - 0.9858 98.58%
Eye irritation - 0.8795 87.95%
Skin irritation - 0.8539 85.39%
Skin corrosion - 0.9765 97.65%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8303 83.03%
Micronuclear + 0.6359 63.59%
Hepatotoxicity - 0.7195 71.95%
skin sensitisation - 0.7421 74.21%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.7560 75.60%
Acute Oral Toxicity (c) III 0.5752 57.52%
Estrogen receptor binding + 0.8201 82.01%
Androgen receptor binding + 0.7335 73.35%
Thyroid receptor binding + 0.7845 78.45%
Glucocorticoid receptor binding + 0.8390 83.90%
Aromatase binding - 0.5685 56.85%
PPAR gamma + 0.6229 62.29%
Honey bee toxicity - 0.8122 81.22%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9780 97.80%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.16% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 94.97% 92.94%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.43% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.73% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.28% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.42% 97.09%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 85.33% 97.31%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.18% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.23% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.31% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.17% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.38% 89.00%
CHEMBL2535 P11166 Glucose transporter 80.03% 98.75%

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.
Aglaia tomentosa subsp. cordata

Cross-Links

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PubChem 11741714
NPASS NPC42204