(25s)-spirost-5-ene-1beta,3beta-diol 1-O-beta-d-fucopyranoside

Details

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Internal ID ab072951-c29b-4ad0-9c21-5acf00490ccf
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins
IUPAC Name (2R,3R,4S,5R,6R)-2-[(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-6-methyloxane-3,4,5-triol
SMILES (Canonical) CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)O)O)C)C)C)OC1
SMILES (Isomeric) C[C@H]1CC[C@@]2([C@H]([C@H]3[C@@H](O2)C[C@@H]4[C@@]3(CC[C@H]5[C@H]4CC=C6[C@@]5([C@@H](C[C@@H](C6)O)O[C@H]7[C@@H]([C@H]([C@H]([C@H](O7)C)O)O)O)C)C)C)OC1
InChI InChI=1S/C33H52O8/c1-16-8-11-33(38-15-16)17(2)26-24(41-33)14-23-21-7-6-19-12-20(34)13-25(32(19,5)22(21)9-10-31(23,26)4)40-30-29(37)28(36)27(35)18(3)39-30/h6,16-18,20-30,34-37H,7-15H2,1-5H3/t16-,17-,18+,20+,21+,22-,23-,24-,25+,26-,27-,28-,29+,30-,31-,32-,33+/m0/s1
InChI Key KIAIAZNJHWWAFM-LZUXFAODSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C33H52O8
Molecular Weight 576.80 g/mol
Exact Mass 576.36621861 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.54
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (25s)-spirost-5-ene-1beta,3beta-diol 1-O-beta-d-fucopyranoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9110 91.10%
Caco-2 - 0.8309 83.09%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7118 71.18%
OATP2B1 inhibitior - 0.7189 71.89%
OATP1B1 inhibitior + 0.8977 89.77%
OATP1B3 inhibitior + 0.9561 95.61%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.6244 62.44%
P-glycoprotein inhibitior + 0.6109 61.09%
P-glycoprotein substrate + 0.5084 50.84%
CYP3A4 substrate + 0.7431 74.31%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8129 81.29%
CYP3A4 inhibition - 0.9134 91.34%
CYP2C9 inhibition - 0.9241 92.41%
CYP2C19 inhibition - 0.9494 94.94%
CYP2D6 inhibition - 0.9206 92.06%
CYP1A2 inhibition - 0.8639 86.39%
CYP2C8 inhibition + 0.7417 74.17%
CYP inhibitory promiscuity - 0.9315 93.15%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4723 47.23%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9413 94.13%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9358 93.58%
Ames mutagenesis - 0.8154 81.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7306 73.06%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.8000 80.00%
skin sensitisation - 0.8809 88.09%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6703 67.03%
Acute Oral Toxicity (c) I 0.4129 41.29%
Estrogen receptor binding + 0.6574 65.74%
Androgen receptor binding + 0.7052 70.52%
Thyroid receptor binding - 0.6260 62.60%
Glucocorticoid receptor binding + 0.5694 56.94%
Aromatase binding + 0.6765 67.65%
PPAR gamma + 0.5421 54.21%
Honey bee toxicity - 0.5786 57.86%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9484 94.84%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.22% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.98% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.82% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 93.66% 95.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.83% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.29% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.70% 89.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 90.05% 95.89%
CHEMBL221 P23219 Cyclooxygenase-1 88.27% 90.17%
CHEMBL332 P03956 Matrix metalloproteinase-1 84.01% 94.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.95% 95.89%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 83.91% 89.05%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.42% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 83.31% 94.73%
CHEMBL2243 O00519 Anandamide amidohydrolase 82.40% 97.53%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.76% 86.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.38% 92.62%
CHEMBL5255 O00206 Toll-like receptor 4 80.94% 92.50%

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.
Nolina microcarpa
Rhodiola rosea

Cross-Links

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PubChem 21630154
NPASS NPC292465
LOTUS LTS0152514
wikiData Q105141416