(1S,4aS,7aS)-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid

Details

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Internal ID 3d28d122-c124-4714-9591-9189a7472936
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Iridoid O-glycosides
IUPAC Name (1S,4aS,7aS)-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H32O14/c1-36-16-7-12(8-17(37-2)21(16)30)3-6-19(29)38-11-18-22(31)23(32)24(33)27(40-18)41-26-20-13(9-28)4-5-14(20)15(10-39-26)25(34)35/h3-4,6-8,10,14,18,20,22-24,26-28,30-33H,5,9,11H2,1-2H3,(H,34,35)/b6-3+/t14-,18-,20-,22-,23+,24-,26+,27+/m1/s1
InChI Key LOIZMVRTZLZNEZ-MICOAVFVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H32O14
Molecular Weight 580.50 g/mol
Exact Mass 580.17920569 g/mol
Topological Polar Surface Area (TPSA) 211.00 Ų
XlogP -1.00
Atomic LogP (AlogP) -0.33
H-Bond Acceptor 13
H-Bond Donor 6
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,4aS,7aS)-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6581 65.81%
Caco-2 - 0.8970 89.70%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6590 65.90%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.7488 74.88%
OATP1B3 inhibitior + 0.9672 96.72%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6681 66.81%
P-glycoprotein inhibitior + 0.5805 58.05%
P-glycoprotein substrate - 0.5519 55.19%
CYP3A4 substrate + 0.6543 65.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8611 86.11%
CYP3A4 inhibition - 0.8065 80.65%
CYP2C9 inhibition - 0.8659 86.59%
CYP2C19 inhibition - 0.6837 68.37%
CYP2D6 inhibition - 0.8878 88.78%
CYP1A2 inhibition - 0.8139 81.39%
CYP2C8 inhibition + 0.7007 70.07%
CYP inhibitory promiscuity - 0.7334 73.34%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7084 70.84%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9224 92.24%
Skin irritation - 0.8130 81.30%
Skin corrosion - 0.9538 95.38%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4924 49.24%
Micronuclear - 0.5500 55.00%
Hepatotoxicity - 0.7591 75.91%
skin sensitisation - 0.8071 80.71%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7408 74.08%
Acute Oral Toxicity (c) III 0.4918 49.18%
Estrogen receptor binding + 0.7751 77.51%
Androgen receptor binding + 0.6268 62.68%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6952 69.52%
Aromatase binding + 0.5378 53.78%
PPAR gamma + 0.6742 67.42%
Honey bee toxicity - 0.7968 79.68%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9579 95.79%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.60% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 97.03% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.80% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.37% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.71% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.66% 95.56%
CHEMBL5255 O00206 Toll-like receptor 4 89.17% 92.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.23% 97.09%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 87.07% 98.21%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.98% 89.62%
CHEMBL3401 O75469 Pregnane X receptor 85.71% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.35% 99.17%
CHEMBL3194 P02766 Transthyretin 84.83% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.19% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.17% 95.89%
CHEMBL5028 O14672 ADAM10 81.16% 97.50%
CHEMBL340 P08684 Cytochrome P450 3A4 81.12% 91.19%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.57% 96.61%

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.
Gardenia jasminoides

Cross-Links

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PubChem 163193649
LOTUS LTS0185344
wikiData Q105154745