[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicene-3-carboxylate

Details

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Internal ID 421bfd4a-f4cc-4410-baee-3e34a4c620d4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name [3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicene-3-carboxylate
SMILES (Canonical) CC1(CCC2(CCC3(C(C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C)C)C)C)C
SMILES (Isomeric) CC1(CCC2(CCC3(C(C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C)C)C)C)C
InChI InChI=1S/C37H62O7/c1-32(2)15-16-34(5)17-18-36(7)21(23(34)19-32)9-10-26-35(6)13-11-22(33(3,4)25(35)12-14-37(26,36)8)30(42)44-31-29(41)28(40)27(39)24(20-38)43-31/h21-29,31,38-41H,9-20H2,1-8H3
InChI Key QELVEUXLDYNPCQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C37H62O7
Molecular Weight 618.90 g/mol
Exact Mass 618.44955431 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 8.60
Atomic LogP (AlogP) 5.85
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicene-3-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6277 62.77%
Caco-2 - 0.8370 83.70%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8394 83.94%
OATP2B1 inhibitior - 0.5748 57.48%
OATP1B1 inhibitior + 0.8679 86.79%
OATP1B3 inhibitior + 0.8208 82.08%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8609 86.09%
P-glycoprotein inhibitior + 0.6936 69.36%
P-glycoprotein substrate - 0.8239 82.39%
CYP3A4 substrate + 0.7205 72.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8612 86.12%
CYP3A4 inhibition - 0.8771 87.71%
CYP2C9 inhibition - 0.8231 82.31%
CYP2C19 inhibition - 0.8775 87.75%
CYP2D6 inhibition - 0.9636 96.36%
CYP1A2 inhibition - 0.7639 76.39%
CYP2C8 inhibition + 0.4682 46.82%
CYP inhibitory promiscuity - 0.9554 95.54%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7481 74.81%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9233 92.33%
Skin irritation - 0.7315 73.15%
Skin corrosion - 0.9603 96.03%
Ames mutagenesis - 0.6470 64.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6629 66.29%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.8263 82.63%
skin sensitisation - 0.9266 92.66%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.7867 78.67%
Acute Oral Toxicity (c) III 0.6703 67.03%
Estrogen receptor binding + 0.5819 58.19%
Androgen receptor binding + 0.7194 71.94%
Thyroid receptor binding - 0.5968 59.68%
Glucocorticoid receptor binding + 0.6445 64.45%
Aromatase binding + 0.6815 68.15%
PPAR gamma + 0.5801 58.01%
Honey bee toxicity - 0.6412 64.12%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5955 59.55%
Fish aquatic toxicity + 0.9124 91.24%

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
CHEMBL218 P21554 Cannabinoid CB1 receptor 98.37% 96.61%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.93% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.12% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.45% 97.09%
CHEMBL237 P41145 Kappa opioid receptor 93.75% 98.10%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.32% 91.11%
CHEMBL2243 O00519 Anandamide amidohydrolase 87.11% 97.53%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 86.47% 95.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.43% 100.00%
CHEMBL204 P00734 Thrombin 85.07% 96.01%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 84.12% 91.24%
CHEMBL221 P23219 Cyclooxygenase-1 83.43% 90.17%
CHEMBL5255 O00206 Toll-like receptor 4 83.43% 92.50%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.89% 96.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.80% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.47% 95.89%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.61% 94.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.24% 96.21%
CHEMBL2581 P07339 Cathepsin D 80.67% 98.95%

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.
Taverniera aegyptiaca

Cross-Links

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PubChem 162868679
LOTUS LTS0020885
wikiData Q105219289