(-)-Thalmiculine

Details

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Internal ID 49c65f28-c6bc-4f2e-8434-ecb17e1ba30e
Taxonomy Lignans, neolignans and related compounds
IUPAC Name (12S,25S)-4,5,20,31-tetramethoxy-11,26-dimethyl-2,18-dioxa-11,26-diazaheptacyclo[23.6.2.214,17.119,23.03,8.07,12.029,33]hexatriaconta-1(31),3(8),4,6,14(36),15,17(35),19,21,23(34),29,32-dodecaen-30-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C38H42N2O7/c1-39-15-13-25-27-21-34(37(44-5)35(25)41)47-36-26-14-16-40(2)29(28(26)20-33(43-4)38(36)45-6)17-22-7-10-24(11-8-22)46-32-19-23(18-30(27)39)9-12-31(32)42-3/h7-12,19-21,29-30,41H,13-18H2,1-6H3/t29-,30-/m0/s1
InChI Key DPEKXFZXWPFXLP-KYJUHHDHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C38H42N2O7
Molecular Weight 638.70 g/mol
Exact Mass 638.29920168 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 6.30
Atomic LogP (AlogP) 6.87
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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Thalmiculine
106146-69-4

2D Structure

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2D Structure of (-)-Thalmiculine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8495 84.95%
Caco-2 + 0.5657 56.57%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.3936 39.36%
OATP2B1 inhibitior - 0.8553 85.53%
OATP1B1 inhibitior + 0.9076 90.76%
OATP1B3 inhibitior + 0.9366 93.66%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 1.0000 100.00%
P-glycoprotein inhibitior + 0.9287 92.87%
P-glycoprotein substrate + 0.5639 56.39%
CYP3A4 substrate + 0.6565 65.65%
CYP2C9 substrate + 0.7890 78.90%
CYP2D6 substrate + 0.7253 72.53%
CYP3A4 inhibition - 0.8348 83.48%
CYP2C9 inhibition - 0.9204 92.04%
CYP2C19 inhibition - 0.9348 93.48%
CYP2D6 inhibition - 0.8976 89.76%
CYP1A2 inhibition - 0.8546 85.46%
CYP2C8 inhibition + 0.6571 65.71%
CYP inhibitory promiscuity - 0.9776 97.76%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6759 67.59%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9353 93.53%
Skin irritation - 0.7625 76.25%
Skin corrosion - 0.9472 94.72%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9388 93.88%
Micronuclear + 0.5600 56.00%
Hepatotoxicity - 0.7966 79.66%
skin sensitisation - 0.8920 89.20%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.9170 91.70%
Acute Oral Toxicity (c) III 0.6540 65.40%
Estrogen receptor binding + 0.7613 76.13%
Androgen receptor binding + 0.7452 74.52%
Thyroid receptor binding + 0.6319 63.19%
Glucocorticoid receptor binding + 0.8627 86.27%
Aromatase binding + 0.6140 61.40%
PPAR gamma + 0.6653 66.53%
Honey bee toxicity - 0.7611 76.11%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.8453 84.53%

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 99.16% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.63% 91.11%
CHEMBL2056 P21728 Dopamine D1 receptor 93.35% 91.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.12% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.68% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.91% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.71% 93.40%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.50% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.08% 95.89%
CHEMBL5747 Q92793 CREB-binding protein 87.84% 95.12%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.66% 93.99%
CHEMBL2535 P11166 Glucose transporter 87.59% 98.75%
CHEMBL2581 P07339 Cathepsin D 87.24% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.08% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 86.51% 91.49%
CHEMBL4208 P20618 Proteasome component C5 86.14% 90.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.00% 89.62%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 84.32% 82.38%
CHEMBL4302 P08183 P-glycoprotein 1 83.78% 92.98%
CHEMBL2413 P32246 C-C chemokine receptor type 1 82.89% 89.50%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.60% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.47% 90.71%
CHEMBL217 P14416 Dopamine D2 receptor 82.40% 95.62%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 82.20% 95.78%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.79% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.78% 94.00%

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 cultratum

Cross-Links

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PubChem 184621
LOTUS LTS0261230
wikiData Q104986462