N-Desmethylthalrugosidine

Details

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Internal ID fbaf5f0c-9a69-49ec-9e93-a1ca907fb8b0
Taxonomy Lignans, neolignans and related compounds
IUPAC Name (3S,22S)-10,11,16,27-tetramethoxy-4-methyl-13,29-dioxa-4,21-diazaheptacyclo[28.2.2.114,18.124,28.03,8.07,12.022,36]hexatriaconta-1(33),7(12),8,10,14(36),15,17,24(35),25,27,30(34),31-dodecaen-15-ol
SMILES (Canonical) CN1CCC2=C3C(=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6)OC)O)OC)OC)OC
SMILES (Isomeric) CN1CCC2=C3C(=C(C=C2[C@@H]1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)C[C@H]6C7=C(O3)C(=C(C=C7CCN6)OC)O)OC)OC)OC
InChI InChI=1S/C37H40N2O7/c1-39-15-13-25-26-20-32(43-4)36(44-5)35(25)46-37-33-23(19-31(42-3)34(37)40)12-14-38-27(33)16-22-8-11-29(41-2)30(18-22)45-24-9-6-21(7-10-24)17-28(26)39/h6-11,18-20,27-28,38,40H,12-17H2,1-5H3/t27-,28-/m0/s1
InChI Key MSEKZZNGEVAPPO-NSOVKSMOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C37H40N2O7
Molecular Weight 624.70 g/mol
Exact Mass 624.28355162 g/mol
Topological Polar Surface Area (TPSA) 90.90 Ų
XlogP 5.80
Atomic LogP (AlogP) 6.53
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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Thalidasan-7-ol, 6,6',7',12-tetramethoxy-2'-methyl-
74683-04-8
Thalidasan-7-ol, 6,6,7,12-tetramethoxy-2-methyl-
N2-Demethylthalrugosidine
CHEMBL3577068
DTXSID80225658
C37H40N2O7
C37-H40-N2-O7

2D Structure

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2D Structure of N-Desmethylthalrugosidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7908 79.08%
Caco-2 + 0.4909 49.09%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.6772 67.72%
OATP2B1 inhibitior - 0.7186 71.86%
OATP1B1 inhibitior + 0.8980 89.80%
OATP1B3 inhibitior + 0.9417 94.17%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9908 99.08%
P-glycoprotein inhibitior + 0.9285 92.85%
P-glycoprotein substrate + 0.7338 73.38%
CYP3A4 substrate + 0.6992 69.92%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate + 0.7102 71.02%
CYP3A4 inhibition - 0.9272 92.72%
CYP2C9 inhibition - 0.9394 93.94%
CYP2C19 inhibition - 0.9392 93.92%
CYP2D6 inhibition - 0.9464 94.64%
CYP1A2 inhibition - 0.9322 93.22%
CYP2C8 inhibition + 0.7118 71.18%
CYP inhibitory promiscuity - 0.9852 98.52%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6597 65.97%
Eye corrosion - 0.9857 98.57%
Eye irritation - 0.9474 94.74%
Skin irritation - 0.7660 76.60%
Skin corrosion - 0.9412 94.12%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8866 88.66%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation - 0.8791 87.91%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.9091 90.91%
Acute Oral Toxicity (c) III 0.5946 59.46%
Estrogen receptor binding + 0.8104 81.04%
Androgen receptor binding + 0.7025 70.25%
Thyroid receptor binding + 0.7046 70.46%
Glucocorticoid receptor binding + 0.8940 89.40%
Aromatase binding + 0.6725 67.25%
PPAR gamma + 0.6543 65.43%
Honey bee toxicity - 0.6986 69.86%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.6661 66.61%

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 99.29% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 96.97% 93.99%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.87% 94.45%
CHEMBL2056 P21728 Dopamine D1 receptor 94.23% 91.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.89% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.83% 85.14%
CHEMBL217 P14416 Dopamine D2 receptor 92.79% 95.62%
CHEMBL2535 P11166 Glucose transporter 90.64% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.51% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.32% 95.89%
CHEMBL2581 P07339 Cathepsin D 89.80% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.26% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.98% 97.09%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 87.82% 89.62%
CHEMBL1951 P21397 Monoamine oxidase A 85.96% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.76% 95.56%
CHEMBL4208 P20618 Proteasome component C5 85.04% 90.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 85.03% 91.03%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.87% 99.17%
CHEMBL2413 P32246 C-C chemokine receptor type 1 83.51% 89.50%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.36% 93.40%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 83.34% 95.78%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 81.76% 90.95%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 81.66% 95.53%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 81.18% 82.38%
CHEMBL4302 P08183 P-glycoprotein 1 80.64% 92.98%

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.
Thalictrum alpinum
Thalictrum flavum

Cross-Links

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PubChem 156760
NPASS NPC48490
ChEMBL CHEMBL3577068
LOTUS LTS0068482
wikiData Q83104724