Tragopogonsaponin N

Details

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Internal ID 2cce7e67-d022-44cc-96eb-4516ae7406be
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name 3,4,5-trihydroxy-6-[[8-hydroxy-8a-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(E)-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyl]oxyoxan-2-yl]oxycarbonyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]oxane-2-carboxylic acid
SMILES (Canonical) CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C(=O)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)OC(=O)C=CC9=CC=C(C=C9)OC1C(C(C(C(O1)CO)O)O)O)C
SMILES (Isomeric) CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C(=O)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)OC(=O)/C=C/C9=CC=C(C=C9)OC1C(C(C(C(O1)CO)O)O)O)C
InChI InChI=1S/C62H90O26/c1-57(2)20-21-62(30(22-57)29-13-14-35-59(5)18-17-37(84-54-47(76)43(72)44(73)49(87-54)51(77)78)58(3,4)34(59)16-19-60(35,6)61(29,7)23-36(62)66)56(79)88-55-50(48(31(65)26-80-55)86-53-46(75)42(71)40(69)33(25-64)83-53)85-38(67)15-10-27-8-11-28(12-9-27)81-52-45(74)41(70)39(68)32(24-63)82-52/h8-13,15,30-37,39-50,52-55,63-66,68-76H,14,16-26H2,1-7H3,(H,77,78)/b15-10+
InChI Key OAGSYWJOJWVKBS-XNTDXEJSSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C62H90O26
Molecular Weight 1251.40 g/mol
Exact Mass 1250.57203297 g/mol
Topological Polar Surface Area (TPSA) 418.00 Ų
XlogP 2.70
Atomic LogP (AlogP) -0.71
H-Bond Acceptor 25
H-Bond Donor 14
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tragopogonsaponin N

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8567 85.67%
Caco-2 - 0.8629 86.29%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.8317 83.17%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.6991 69.91%
OATP1B3 inhibitior - 0.4152 41.52%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6276 62.76%
BSEP inhibitior + 0.9618 96.18%
P-glycoprotein inhibitior + 0.7439 74.39%
P-glycoprotein substrate + 0.5380 53.80%
CYP3A4 substrate + 0.7476 74.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8783 87.83%
CYP3A4 inhibition - 0.7238 72.38%
CYP2C9 inhibition - 0.8199 81.99%
CYP2C19 inhibition - 0.8379 83.79%
CYP2D6 inhibition - 0.9279 92.79%
CYP1A2 inhibition - 0.7832 78.32%
CYP2C8 inhibition + 0.8333 83.33%
CYP inhibitory promiscuity - 0.9494 94.94%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5954 59.54%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.8972 89.72%
Skin irritation - 0.6597 65.97%
Skin corrosion - 0.9443 94.43%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7634 76.34%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.8750 87.50%
skin sensitisation - 0.8902 89.02%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.9368 93.68%
Acute Oral Toxicity (c) III 0.6582 65.82%
Estrogen receptor binding + 0.6971 69.71%
Androgen receptor binding + 0.7539 75.39%
Thyroid receptor binding + 0.6891 68.91%
Glucocorticoid receptor binding + 0.8033 80.33%
Aromatase binding + 0.6538 65.38%
PPAR gamma + 0.8224 82.24%
Honey bee toxicity - 0.6416 64.16%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9878 98.78%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.70% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.68% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.89% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.54% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.27% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.06% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.43% 89.00%
CHEMBL226 P30542 Adenosine A1 receptor 90.18% 95.93%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.89% 96.00%
CHEMBL221 P23219 Cyclooxygenase-1 87.93% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.42% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.09% 99.17%
CHEMBL5028 O14672 ADAM10 85.64% 97.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.65% 93.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.01% 95.50%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 82.08% 89.67%
CHEMBL2581 P07339 Cathepsin D 81.64% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.60% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.45% 92.62%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.62% 91.07%

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.
Tragopogon porrifolius

Cross-Links

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PubChem 14827938
LOTUS LTS0234062
wikiData Q105188662