5,6,6',7,12-Pentamethoxy-2-methyl-1',2'-didehydroberbaman

Details

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Internal ID 6d9c4946-5f64-40d0-8ebc-f9e190f4b061
Taxonomy Phenylpropanoids and polyketides > Tannins
IUPAC Name 9,19,20,21,25-pentamethoxy-15-methyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-1(30),3(36),4,6(35),8,10,12(34),18(33),19,21,24,26,31-tridecaene
SMILES (Canonical) CN1CCC2=C3C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6=NCCC7=CC(=C(C=C76)OC3=C(C(=C2OC)OC)OC)OC)C=C5
SMILES (Isomeric) CN1CCC2=C3C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6=NCCC7=CC(=C(C=C76)OC3=C(C(=C2OC)OC)OC)OC)C=C5
InChI InChI=1S/C38H40N2O7/c1-40-16-14-26-34-29(40)18-23-9-12-30(41-2)32(19-23)46-25-10-7-22(8-11-25)17-28-27-21-33(31(42-3)20-24(27)13-15-39-28)47-36(34)38(45-6)37(44-5)35(26)43-4/h7-12,19-21,29H,13-18H2,1-6H3
InChI Key YWNUNVSMOKMJMG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C38H40N2O7
Molecular Weight 636.70 g/mol
Exact Mass 636.28355162 g/mol
Topological Polar Surface Area (TPSA) 80.20 Ų
XlogP 5.80
Atomic LogP (AlogP) 6.99
H-Bond Acceptor 9
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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5,6,6',7,12-Pentamethoxy-2-methyl-1',2'-didehydroberbaman

2D Structure

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2D Structure of 5,6,6',7,12-Pentamethoxy-2-methyl-1',2'-didehydroberbaman

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8290 82.90%
Caco-2 + 0.5584 55.84%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Lysosomes 0.4858 48.58%
OATP2B1 inhibitior - 0.8547 85.47%
OATP1B1 inhibitior + 0.9048 90.48%
OATP1B3 inhibitior + 0.9363 93.63%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.9960 99.60%
P-glycoprotein inhibitior + 0.9590 95.90%
P-glycoprotein substrate + 0.7341 73.41%
CYP3A4 substrate + 0.7126 71.26%
CYP2C9 substrate - 0.6189 61.89%
CYP2D6 substrate + 0.4842 48.42%
CYP3A4 inhibition - 0.6758 67.58%
CYP2C9 inhibition - 0.9360 93.60%
CYP2C19 inhibition - 0.8958 89.58%
CYP2D6 inhibition - 0.8532 85.32%
CYP1A2 inhibition - 0.9075 90.75%
CYP2C8 inhibition + 0.6107 61.07%
CYP inhibitory promiscuity - 0.9644 96.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6257 62.57%
Eye corrosion - 0.9870 98.70%
Eye irritation - 0.9531 95.31%
Skin irritation - 0.7774 77.74%
Skin corrosion - 0.9404 94.04%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9366 93.66%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.8739 87.39%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.8224 82.24%
Acute Oral Toxicity (c) III 0.6864 68.64%
Estrogen receptor binding + 0.7826 78.26%
Androgen receptor binding + 0.6729 67.29%
Thyroid receptor binding + 0.7312 73.12%
Glucocorticoid receptor binding + 0.8623 86.23%
Aromatase binding + 0.6088 60.88%
PPAR gamma + 0.6342 63.42%
Honey bee toxicity - 0.7427 74.27%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.8679 86.79%

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 99.27% 96.09%
CHEMBL4302 P08183 P-glycoprotein 1 97.49% 92.98%
CHEMBL5747 Q92793 CREB-binding protein 96.17% 95.12%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.81% 96.77%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 92.88% 95.78%
CHEMBL2581 P07339 Cathepsin D 92.85% 98.95%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 92.75% 82.38%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 92.53% 93.40%
CHEMBL2056 P21728 Dopamine D1 receptor 91.23% 91.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.91% 95.89%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 89.44% 95.53%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 89.08% 90.95%
CHEMBL2243 O00519 Anandamide amidohydrolase 88.54% 97.53%
CHEMBL1951 P21397 Monoamine oxidase A 88.37% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.62% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.55% 99.17%
CHEMBL5203 P33316 dUTP pyrophosphatase 85.81% 99.18%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.66% 94.00%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 84.06% 95.34%
CHEMBL2094108 P49354 Protein farnesyltransferase 84.05% 97.92%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.00% 93.99%
CHEMBL2535 P11166 Glucose transporter 83.94% 98.75%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 83.65% 91.43%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.61% 95.56%
CHEMBL217 P14416 Dopamine D2 receptor 83.57% 95.62%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 81.79% 82.67%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.77% 95.89%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.34% 100.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.63% 89.62%

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 foliolosum
Thalictrum simplex

Cross-Links

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PubChem 494542
NPASS NPC87364