(25R)-spirost-5-en-3beta,27-diol

Details

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Internal ID 4c46268f-fd7f-4689-991c-c3725dd47b51
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (3S,8S,9S,10R,13S,14S,16S,17R)-17-ethyl-16-[(2S,5S)-5-(hydroxymethyl)-2-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
SMILES (Canonical) CCC1C(CC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)OC5(CCC(CO5)CO)C
SMILES (Isomeric) CC[C@H]1[C@H](C[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)O)C)C)O[C@]5(CC[C@H](CO5)CO)C
InChI InChI=1S/C28H46O4/c1-5-22-25(32-28(4)13-8-18(16-29)17-31-28)15-24-21-7-6-19-14-20(30)9-11-26(19,2)23(21)10-12-27(22,24)3/h6,18,20-25,29-30H,5,7-17H2,1-4H3/t18-,20-,21+,22-,23-,24-,25-,26-,27+,28-/m0/s1
InChI Key YRUXDYYQHRQPTP-RUYDNTASSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H46O4
Molecular Weight 446.70 g/mol
Exact Mass 446.33960994 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 5.10
Atomic LogP (AlogP) 5.47
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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LMST01080063

2D Structure

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2D Structure of (25R)-spirost-5-en-3beta,27-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9684 96.84%
Caco-2 - 0.5628 56.28%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5987 59.87%
OATP2B1 inhibitior - 0.5674 56.74%
OATP1B1 inhibitior + 0.8875 88.75%
OATP1B3 inhibitior + 0.9391 93.91%
MATE1 inhibitior - 0.9212 92.12%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8155 81.55%
P-glycoprotein inhibitior - 0.5231 52.31%
P-glycoprotein substrate + 0.7152 71.52%
CYP3A4 substrate + 0.7384 73.84%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.7891 78.91%
CYP3A4 inhibition - 0.5614 56.14%
CYP2C9 inhibition - 0.8923 89.23%
CYP2C19 inhibition - 0.8644 86.44%
CYP2D6 inhibition - 0.9296 92.96%
CYP1A2 inhibition - 0.8172 81.72%
CYP2C8 inhibition + 0.8068 80.68%
CYP inhibitory promiscuity - 0.7529 75.29%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6258 62.58%
Eye corrosion - 0.9914 99.14%
Eye irritation - 0.9548 95.48%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9509 95.09%
Ames mutagenesis - 0.7519 75.19%
Human Ether-a-go-go-Related Gene inhibition - 0.4191 41.91%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.5851 58.51%
skin sensitisation - 0.9084 90.84%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7671 76.71%
Acute Oral Toxicity (c) III 0.5130 51.30%
Estrogen receptor binding + 0.7750 77.50%
Androgen receptor binding + 0.7697 76.97%
Thyroid receptor binding + 0.6810 68.10%
Glucocorticoid receptor binding + 0.8148 81.48%
Aromatase binding + 0.6446 64.46%
PPAR gamma + 0.6084 60.84%
Honey bee toxicity - 0.7118 71.18%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9599 95.99%

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
CHEMBL226 P30542 Adenosine A1 receptor 98.64% 95.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.07% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.65% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.09% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 94.66% 97.79%
CHEMBL2581 P07339 Cathepsin D 93.94% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.98% 100.00%
CHEMBL242 Q92731 Estrogen receptor beta 91.03% 98.35%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.70% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.91% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.24% 95.89%
CHEMBL1914 P06276 Butyrylcholinesterase 82.37% 95.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.92% 92.62%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.36% 97.28%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.01% 95.89%

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.
Phaseolus vulgaris
Phedimus kamtschaticus

Cross-Links

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PubChem 52931459
NPASS NPC156980