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(2R,3R,4S,4aR,6aR,6bS,8aR,12S,12aS,14aR,14bR)-2,12-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid

Table of Contents

Details
Physical and Chemical Properties
Synonyms
2D Structure
3D Structure
ADMET Properties
Targets (proven and/or predicted)
Plants that contains it
Cross-Links

Details

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Internal ID cb448f7e-c46c-40c1-b7c5-9c78cb92e88b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (2R,3R,4S,4aR,6aR,6bS,8aR,12S,12aS,14aR,14bR)-2,12-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H66O17/c1-37(2)11-13-42(36(55)59-34-30(51)28(49)26(47)21(17-44)57-34)14-12-39(4)18(24(42)31(37)52)7-8-22-38(3)15-19(45)32(41(6,35(53)54)23(38)9-10-40(22,39)5)58-33-29(50)27(48)25(46)20(16-43)56-33/h7,19-34,43-52H,8-17H2,1-6H3,(H,53,54)/t19-,20-,21-,22-,23-,24-,25-,26-,27+,28+,29-,30-,31+,32+,33+,34+,38-,39-,40-,41+,42+/m1/s1
InChI Key GGRXMTBPGLVDIB-JOZODPSFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C42H66O17
Molecular Weight 843.00 g/mol
Exact Mass 842.43000063 g/mol
Topological Polar Surface Area (TPSA) 294.00 Ų
XlogP 0.50
Atomic LogP (AlogP) -0.68
H-Bond Acceptor 16
H-Bond Donor 11
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3R,4S,4aR,6aR,6bS,8aR,12S,12aS,14aR,14bR)-2,12-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-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 + 0.7601 76.01%
Caco-2 - 0.8848 88.48%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.8703 87.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8188 81.88%
OATP1B3 inhibitior - 0.4610 46.10%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5026 50.26%
BSEP inhibitior + 0.6170 61.70%
P-glycoprotein inhibitior + 0.7469 74.69%
P-glycoprotein substrate - 0.6783 67.83%
CYP3A4 substrate + 0.6972 69.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8776 87.76%
CYP3A4 inhibition - 0.8310 83.10%
CYP2C9 inhibition - 0.8704 87.04%
CYP2C19 inhibition - 0.9216 92.16%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.9009 90.09%
CYP2C8 inhibition + 0.6624 66.24%
CYP inhibitory promiscuity - 0.9733 97.33%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6024 60.24%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.9073 90.73%
Skin irritation - 0.5876 58.76%
Skin corrosion - 0.9441 94.41%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7211 72.11%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.8625 86.25%
skin sensitisation - 0.9013 90.13%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.5652 56.52%
Acute Oral Toxicity (c) III 0.8023 80.23%
Estrogen receptor binding + 0.7719 77.19%
Androgen receptor binding + 0.7405 74.05%
Thyroid receptor binding - 0.5775 57.75%
Glucocorticoid receptor binding + 0.6612 66.12%
Aromatase binding + 0.6083 60.83%
PPAR gamma + 0.7555 75.55%
Honey bee toxicity - 0.7764 77.64%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6450 64.50%
Fish aquatic toxicity + 0.9585 95.85%

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 99.13% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.72% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.16% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.29% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.40% 94.45%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 87.94% 96.21%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.45% 97.36%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.40% 93.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.06% 97.25%
CHEMBL2581 P07339 Cathepsin D 83.00% 98.95%
CHEMBL5255 O00206 Toll-like receptor 4 82.69% 92.50%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.51% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.10% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.07% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.64% 95.50%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.38% 91.07%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.34% 95.17%

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.
Trachelospermum asiaticum

Cross-Links

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PubChem 163014299
LOTUS LTS0000818
wikiData Q105008301