(16alpha,20R,22S,23S)-16,23:22,25-diepoxy-2,20,22,23-tetrahydroxycucurbita-1,5-diene-3,11-dione 2-O-beta-D-glucopyranoside

Details

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Internal ID c49fe1b9-8a18-477b-9d05-5b0e861eae3f
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides
IUPAC Name (1S,2S,10R,11R,14R,15R,16R,17S,21S,23R)-16,17,21-trihydroxy-1,6,6,11,14,16,19,19-octamethyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-18,22-dioxahexacyclo[12.10.0.02,11.05,10.015,23.017,21]tetracosa-4,8-diene-7,12-dione
SMILES (Canonical) CC1(CC2(C(O1)(C(C3C(O2)CC4(C3(CC(=O)C5(C4CC=C6C5C=C(C(=O)C6(C)C)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)(C)O)O)O)C
SMILES (Isomeric) C[C@@]12C[C@@H]3[C@@H]([C@]1(CC(=O)[C@@]4([C@H]2CC=C5[C@H]4C=C(C(=O)C5(C)C)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)C)C)[C@@]([C@]7([C@@](O3)(CC(O7)(C)C)O)O)(C)O
InChI InChI=1S/C36H52O13/c1-29(2)15-35(44)36(45,49-29)34(8,43)26-19(48-35)12-31(5)21-10-9-16-17(33(21,7)22(38)13-32(26,31)6)11-18(27(42)30(16,3)4)46-28-25(41)24(40)23(39)20(14-37)47-28/h9,11,17,19-21,23-26,28,37,39-41,43-45H,10,12-15H2,1-8H3/t17-,19-,20-,21+,23-,24+,25-,26+,28-,31+,32-,33+,34-,35+,36+/m1/s1
InChI Key ANFGZMJFIDODOI-JOWNWPMHSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C36H52O13
Molecular Weight 692.80 g/mol
Exact Mass 692.34079171 g/mol
Topological Polar Surface Area (TPSA) 213.00 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.60
H-Bond Acceptor 13
H-Bond Donor 7
Rotatable Bonds 3

Synonyms

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CHEBI:68908
(16alpha,20R,22S,23S)-16,23:22,25-diepoxy-2,20,22,23-tetrahydroxycucurbita-1,5-diene-3,11-dione 2-O-beta-D-glucopyranoside
DTXSID901099974
BDBM50358966
Q27137263
(4aR,4bR,6aR,6bR,7R,7aS,10aS,11aR,12aS,12bS)-7,7a,10a-trihydroxy-1,1,4b,6a,7,9,9,12a-octamethyl-2,5-dioxo-1,2,4a,4b,5,6,6a,6b,7,7a,9,10,10a,11a,12,12a,12b,13-octadecahydrofuro[3,2-b]naphtho[2',1':4,5]indeno[1,2-e]pyran-3-yl beta-D-glucopyranoside
1345690-55-2
19-Norlanosta-1,5-diene-3,11,22,23-tetrone, 2-(beta-D-glucopyranosyloxy)-16,20,25-trihydroxy-9-methyl-, cyclic 22,25:23,16-dihemiacetal, (9beta,10alpha,16alpha,22S,23S)-

2D Structure

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2D Structure of (16alpha,20R,22S,23S)-16,23:22,25-diepoxy-2,20,22,23-tetrahydroxycucurbita-1,5-diene-3,11-dione 2-O-beta-D-glucopyranoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9062 90.62%
Caco-2 - 0.8543 85.43%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.8391 83.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8469 84.69%
OATP1B3 inhibitior + 0.8941 89.41%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.5869 58.69%
P-glycoprotein inhibitior + 0.7502 75.02%
P-glycoprotein substrate - 0.5492 54.92%
CYP3A4 substrate + 0.7002 70.02%
CYP2C9 substrate - 0.8050 80.50%
CYP2D6 substrate - 0.8811 88.11%
CYP3A4 inhibition - 0.7178 71.78%
CYP2C9 inhibition - 0.8548 85.48%
CYP2C19 inhibition - 0.9332 93.32%
CYP2D6 inhibition - 0.9448 94.48%
CYP1A2 inhibition - 0.9130 91.30%
CYP2C8 inhibition + 0.6241 62.41%
CYP inhibitory promiscuity - 0.9153 91.53%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5063 50.63%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9107 91.07%
Skin irritation - 0.5232 52.32%
Skin corrosion - 0.9405 94.05%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6709 67.09%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.7593 75.93%
skin sensitisation - 0.8895 88.95%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.7164 71.64%
Acute Oral Toxicity (c) III 0.5091 50.91%
Estrogen receptor binding + 0.7117 71.17%
Androgen receptor binding + 0.7554 75.54%
Thyroid receptor binding + 0.5564 55.64%
Glucocorticoid receptor binding + 0.7585 75.85%
Aromatase binding + 0.7010 70.10%
PPAR gamma + 0.7157 71.57%
Honey bee toxicity - 0.6985 69.85%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6250 62.50%
Fish aquatic toxicity + 0.9827 98.27%

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 98.68% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.93% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 96.22% 96.61%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.19% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.72% 85.14%
CHEMBL2581 P07339 Cathepsin D 93.55% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.65% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.00% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.32% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.42% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 86.08% 94.73%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.79% 96.77%
CHEMBL221 P23219 Cyclooxygenase-1 81.69% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.89% 95.89%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.58% 96.95%

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.
There are no matching plants.

Cross-Links

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PubChem 56655720
LOTUS LTS0026772
wikiData Q27137263