(4aR,5R,6aS,6bR,9R,10S,12aR)-5-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

Details

Top
Internal ID 848463e9-0a5e-4ccc-b189-52f6616680a2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (4aR,5R,6aS,6bR,9R,10S,12aR)-5-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
SMILES (Canonical) CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)CO)OC6C(C(C(CO6)O)O)O)C)C(=O)O)C
SMILES (Isomeric) C[C@]12CC[C@@H]([C@@](C1CC[C@@]3(C2CC=C4[C@]3(C[C@H]([C@@]5(C4CC(CC5)(C)C)C(=O)O)O)C)C)(C)CO)O[C@H]6[C@@H]([C@H]([C@H](CO6)O)O)O
InChI InChI=1S/C35H56O9/c1-30(2)13-14-35(29(41)42)20(15-30)19-7-8-23-31(3)11-10-25(44-28-27(40)26(39)21(37)17-43-28)32(4,18-36)22(31)9-12-33(23,5)34(19,6)16-24(35)38/h7,20-28,36-40H,8-18H2,1-6H3,(H,41,42)/t20?,21-,22?,23?,24+,25-,26-,27+,28-,31-,32-,33+,34+,35+/m0/s1
InChI Key FCPRBNDLDDAHLC-IJRDZWOMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C35H56O9
Molecular Weight 620.80 g/mol
Exact Mass 620.39243336 g/mol
Topological Polar Surface Area (TPSA) 157.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.64
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (4aR,5R,6aS,6bR,9R,10S,12aR)-5-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8280 82.80%
Caco-2 - 0.8281 82.81%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8569 85.69%
OATP2B1 inhibitior - 0.5754 57.54%
OATP1B1 inhibitior + 0.8473 84.73%
OATP1B3 inhibitior - 0.5000 50.00%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6526 65.26%
BSEP inhibitior - 0.4744 47.44%
P-glycoprotein inhibitior + 0.6736 67.36%
P-glycoprotein substrate - 0.6296 62.96%
CYP3A4 substrate + 0.7094 70.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8798 87.98%
CYP3A4 inhibition - 0.8968 89.68%
CYP2C9 inhibition - 0.8549 85.49%
CYP2C19 inhibition - 0.8686 86.86%
CYP2D6 inhibition - 0.9356 93.56%
CYP1A2 inhibition - 0.8265 82.65%
CYP2C8 inhibition + 0.6121 61.21%
CYP inhibitory promiscuity - 0.9540 95.40%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6921 69.21%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.9229 92.29%
Skin irritation - 0.6263 62.63%
Skin corrosion - 0.9494 94.94%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7154 71.54%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.8569 85.69%
skin sensitisation - 0.8865 88.65%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.7126 71.26%
Acute Oral Toxicity (c) III 0.8000 80.00%
Estrogen receptor binding + 0.6261 62.61%
Androgen receptor binding + 0.7196 71.96%
Thyroid receptor binding - 0.5736 57.36%
Glucocorticoid receptor binding + 0.6105 61.05%
Aromatase binding + 0.6451 64.51%
PPAR gamma + 0.6114 61.14%
Honey bee toxicity - 0.8249 82.49%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6650 66.50%
Fish aquatic toxicity + 0.9499 94.99%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.79% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.42% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.21% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.03% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.45% 95.56%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.15% 91.07%
CHEMBL5028 O14672 ADAM10 84.83% 97.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.36% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.74% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.70% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.15% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.95% 96.77%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.49% 92.62%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.30% 94.33%

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.
Caltha palustris
Caulophyllum robustum
Caulophyllum thalictroides

Cross-Links

Top
PubChem 6324902
LOTUS LTS0240446
wikiData Q105104904