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

Details

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Internal ID 05a02869-59d8-4db2-91bb-01ec9bd03d30
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1R,4aR,6aR,6aS,6bR,8aS,10S,12aR,14bS)-1-hydroxy-1,6a,6b,9,9,12a-hexamethyl-2-methylidene-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-3H-picene-4a-carboxylic acid
SMILES (Canonical) CC1(C2CCC3(C(C2(CCC1OC4C(C(C(CO4)O)O)O)C)CC=C5C3(CCC6(C5C(C(=C)CC6)(C)O)C(=O)O)C)C)C
SMILES (Isomeric) C[C@]12CC[C@@H](C([C@H]1CC[C@@]3([C@@H]2CC=C4[C@]3(CC[C@@]5([C@H]4[C@@](C(=C)CC5)(C)O)C(=O)O)C)C)(C)C)O[C@H]6[C@@H]([C@H]([C@H](CO6)O)O)O
InChI InChI=1S/C35H54O8/c1-19-10-15-35(29(39)40)17-16-32(5)20(27(35)34(19,7)41)8-9-23-31(4)13-12-24(30(2,3)22(31)11-14-33(23,32)6)43-28-26(38)25(37)21(36)18-42-28/h8,21-28,36-38,41H,1,9-18H2,2-7H3,(H,39,40)/t21-,22+,23+,24-,25-,26+,27+,28-,31-,32+,33+,34-,35-/m0/s1
InChI Key WHTAFFKLEKGYBI-OMUOAVPCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C35H54O8
Molecular Weight 602.80 g/mol
Exact Mass 602.38186868 g/mol
Topological Polar Surface Area (TPSA) 137.00 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.59
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,4aR,6aR,6aS,6bR,8aS,10S,12aR,14bS)-1-hydroxy-1,6a,6b,9,9,12a-hexamethyl-2-methylidene-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-3H-picene-4a-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 + 0.9042 90.42%
Caco-2 - 0.8139 81.39%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8446 84.46%
OATP2B1 inhibitior - 0.5732 57.32%
OATP1B1 inhibitior + 0.7771 77.71%
OATP1B3 inhibitior - 0.2361 23.61%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7068 70.68%
BSEP inhibitior - 0.5512 55.12%
P-glycoprotein inhibitior + 0.6615 66.15%
P-glycoprotein substrate - 0.7027 70.27%
CYP3A4 substrate + 0.7154 71.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8865 88.65%
CYP3A4 inhibition - 0.8231 82.31%
CYP2C9 inhibition - 0.7824 78.24%
CYP2C19 inhibition - 0.8206 82.06%
CYP2D6 inhibition - 0.9269 92.69%
CYP1A2 inhibition - 0.7312 73.12%
CYP2C8 inhibition + 0.6623 66.23%
CYP inhibitory promiscuity - 0.9589 95.89%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6838 68.38%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.9279 92.79%
Skin irritation - 0.5338 53.38%
Skin corrosion - 0.9397 93.97%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3672 36.72%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.8380 83.80%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7227 72.27%
Acute Oral Toxicity (c) III 0.6912 69.12%
Estrogen receptor binding + 0.6269 62.69%
Androgen receptor binding + 0.7288 72.88%
Thyroid receptor binding - 0.5572 55.72%
Glucocorticoid receptor binding + 0.6139 61.39%
Aromatase binding + 0.6632 66.32%
PPAR gamma + 0.6263 62.63%
Honey bee toxicity - 0.7573 75.73%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5955 59.55%
Fish aquatic toxicity + 0.9883 98.83%

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 96.49% 91.11%
CHEMBL340 P08684 Cytochrome P450 3A4 92.08% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.75% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.44% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.98% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.90% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.42% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.13% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.91% 96.09%
CHEMBL5028 O14672 ADAM10 83.80% 97.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.07% 92.94%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.81% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.42% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.50% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.33% 94.45%

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.
Sanguisorba officinalis

Cross-Links

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PubChem 163062791
LOTUS LTS0110255
wikiData Q105305791