(-)-Thalmiculimine

Details

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Internal ID 96d5180e-676e-4974-8824-4a34016d6de3
Taxonomy Lignans, neolignans and related compounds
IUPAC Name (25S)-4,5,20,31-tetramethoxy-26-methyl-2,18-dioxa-11,26-diazaheptacyclo[23.6.2.214,17.119,23.03,8.07,12.029,33]hexatriaconta-1(31),3(8),4,6,11,14(36),15,17(35),19,21,23(34),29,32-tridecaen-30-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C37H38N2O7/c1-39-15-13-24-27-20-33(36(43-4)34(24)40)46-35-25-12-14-38-28(26(25)19-32(42-3)37(35)44-5)16-21-6-9-23(10-7-21)45-31-18-22(17-29(27)39)8-11-30(31)41-2/h6-11,18-20,29,40H,12-17H2,1-5H3/t29-/m0/s1
InChI Key GLADJWPVQRCRIG-LJAQVGFWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C37H38N2O7
Molecular Weight 622.70 g/mol
Exact Mass 622.26790156 g/mol
Topological Polar Surface Area (TPSA) 91.20 Ų
XlogP 5.80
Atomic LogP (AlogP) 6.68
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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Thalmiculimine
105437-18-1
1H-8,9,13-(1,3)Butadien(1)yl(4)ylidene-4,6:15,18-dietheno-20,24-metheno-10H-pyrido(2,3-t)(1,13,6)dioxaazacyclotricosin-34-ol, 2,3,11,14,25,25a-hexahydro-21,31,32,33-tetramethoxy-1-methyl-, (S)-

2D Structure

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2D Structure of (-)-Thalmiculimine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7926 79.26%
Caco-2 - 0.5813 58.13%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Lysosomes 0.3950 39.50%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.8737 87.37%
OATP1B3 inhibitior + 0.9314 93.14%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.9966 99.66%
P-glycoprotein inhibitior + 0.9297 92.97%
P-glycoprotein substrate + 0.7252 72.52%
CYP3A4 substrate + 0.7152 71.52%
CYP2C9 substrate - 0.6166 61.66%
CYP2D6 substrate + 0.4532 45.32%
CYP3A4 inhibition - 0.6601 66.01%
CYP2C9 inhibition - 0.8914 89.14%
CYP2C19 inhibition - 0.9099 90.99%
CYP2D6 inhibition - 0.8632 86.32%
CYP1A2 inhibition - 0.8514 85.14%
CYP2C8 inhibition + 0.7145 71.45%
CYP inhibitory promiscuity - 0.9842 98.42%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6748 67.48%
Eye corrosion - 0.9864 98.64%
Eye irritation - 0.9408 94.08%
Skin irritation - 0.7534 75.34%
Skin corrosion - 0.9388 93.88%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8815 88.15%
Micronuclear + 0.5300 53.00%
Hepatotoxicity - 0.7341 73.41%
skin sensitisation - 0.8723 87.23%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.8935 89.35%
Acute Oral Toxicity (c) III 0.6475 64.75%
Estrogen receptor binding + 0.8208 82.08%
Androgen receptor binding + 0.6929 69.29%
Thyroid receptor binding + 0.7196 71.96%
Glucocorticoid receptor binding + 0.8726 87.26%
Aromatase binding + 0.6990 69.90%
PPAR gamma + 0.6972 69.72%
Honey bee toxicity - 0.7697 76.97%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.8598 85.98%

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 99.53% 96.09%
CHEMBL5747 Q92793 CREB-binding protein 96.32% 95.12%
CHEMBL2056 P21728 Dopamine D1 receptor 93.82% 91.00%
CHEMBL2581 P07339 Cathepsin D 93.75% 98.95%
CHEMBL4302 P08183 P-glycoprotein 1 93.13% 92.98%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 91.84% 82.38%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.38% 95.89%
CHEMBL2535 P11166 Glucose transporter 91.21% 98.75%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 91.19% 95.78%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 89.89% 93.40%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.80% 89.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.41% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.18% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.53% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.21% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.64% 94.00%
CHEMBL1951 P21397 Monoamine oxidase A 87.63% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.98% 85.14%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.67% 96.77%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.18% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.85% 93.99%
CHEMBL2094108 P49354 Protein farnesyltransferase 83.66% 97.92%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.32% 100.00%
CHEMBL217 P14416 Dopamine D2 receptor 83.16% 95.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.61% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.18% 99.23%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 81.13% 95.53%

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 184489
LOTUS LTS0242627
wikiData Q105010705