Trachelosiaside

Details

Top
Internal ID b4122e2f-5d0e-48df-95dc-8744ab1c513e
Taxonomy Lignans, neolignans and related compounds > Lignan glycosides
IUPAC Name (3R,4R)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-[[4-hydroxy-3-methoxy-5-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl]methyl]oxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H32O11/c1-34-18-8-12(3-4-17(18)28)5-14-11-36-26(33)15(14)6-13-7-16(21(29)19(9-13)35-2)25-24(32)23(31)22(30)20(10-27)37-25/h3-4,7-9,14-15,20,22-25,27-32H,5-6,10-11H2,1-2H3/t14-,15+,20+,22+,23-,24+,25-/m0/s1
InChI Key CZGFAWSPACXBMG-OKUUYLHOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C26H32O11
Molecular Weight 520.50 g/mol
Exact Mass 520.19446183 g/mol
Topological Polar Surface Area (TPSA) 175.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.20
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 8

Synonyms

Top
(3R,4R)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-[[4-hydroxy-3-methoxy-5-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl]methyl]oxolan-2-one
HY-133109
CS-0111111

2D Structure

Top
2D Structure of Trachelosiaside

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6089 60.89%
Caco-2 - 0.8736 87.36%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8303 83.03%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.7801 78.01%
OATP1B3 inhibitior + 0.9562 95.62%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.7596 75.96%
P-glycoprotein inhibitior - 0.5098 50.98%
P-glycoprotein substrate - 0.5997 59.97%
CYP3A4 substrate + 0.6196 61.96%
CYP2C9 substrate - 0.5971 59.71%
CYP2D6 substrate - 0.8010 80.10%
CYP3A4 inhibition - 0.7257 72.57%
CYP2C9 inhibition - 0.8382 83.82%
CYP2C19 inhibition - 0.7518 75.18%
CYP2D6 inhibition - 0.9155 91.55%
CYP1A2 inhibition - 0.8751 87.51%
CYP2C8 inhibition + 0.5726 57.26%
CYP inhibitory promiscuity - 0.5055 50.55%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6784 67.84%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.9314 93.14%
Skin irritation - 0.8603 86.03%
Skin corrosion - 0.9609 96.09%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6747 67.47%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.8832 88.32%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.7976 79.76%
Acute Oral Toxicity (c) III 0.7005 70.05%
Estrogen receptor binding + 0.8498 84.98%
Androgen receptor binding + 0.6600 66.00%
Thyroid receptor binding + 0.5238 52.38%
Glucocorticoid receptor binding + 0.5707 57.07%
Aromatase binding - 0.5748 57.48%
PPAR gamma + 0.6153 61.53%
Honey bee toxicity - 0.7829 78.29%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9258 92.58%

Targets

Top

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 99.76% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.42% 96.09%
CHEMBL2581 P07339 Cathepsin D 98.38% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 97.15% 83.82%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.80% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.28% 94.45%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.48% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.08% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.58% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.99% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.75% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.61% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 88.48% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.69% 89.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.09% 96.61%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.99% 97.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.44% 97.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.66% 96.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.94% 99.15%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.95% 95.89%

Plants that contains it

Top
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.
Trachelospermum asiaticum

Cross-Links

Top
PubChem 21636140
LOTUS LTS0265914
wikiData Q104972772