(22R)-5alpha-Cycloarta-23-ene-3beta,22alpha,25-triol

Details

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Internal ID 18920891-c2b7-4e35-a2f9-16479e96b52c
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cycloartanols and derivatives
IUPAC Name (E,5R,6S)-6-[(1S,3R,6S,8R,11S,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-3-ene-2,5-diol
SMILES (Canonical) CC(C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)C(C=CC(C)(C)O)O
SMILES (Isomeric) C[C@@H]([C@H]1CC[C@@]2([C@@]1(CC[C@]34[C@H]2CC[C@@H]5[C@]3(C4)CC[C@@H](C5(C)C)O)C)C)[C@@H](/C=C/C(C)(C)O)O
InChI InChI=1S/C30H50O3/c1-19(21(31)11-13-25(2,3)33)20-10-14-28(7)23-9-8-22-26(4,5)24(32)12-15-29(22)18-30(23,29)17-16-27(20,28)6/h11,13,19-24,31-33H,8-10,12,14-18H2,1-7H3/b13-11+/t19-,20+,21+,22-,23-,24-,27+,28-,29+,30-/m0/s1
InChI Key JQQHNCBIPFJTGF-YDLGJMQMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O3
Molecular Weight 458.70 g/mol
Exact Mass 458.37599545 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 6.80
Atomic LogP (AlogP) 6.11
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (22R)-5alpha-Cycloarta-23-ene-3beta,22alpha,25-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 - 0.6225 62.25%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5915 59.15%
OATP2B1 inhibitior - 0.7188 71.88%
OATP1B1 inhibitior + 0.8885 88.85%
OATP1B3 inhibitior + 0.9520 95.20%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.7579 75.79%
P-glycoprotein inhibitior - 0.5992 59.92%
P-glycoprotein substrate - 0.7410 74.10%
CYP3A4 substrate + 0.6313 63.13%
CYP2C9 substrate - 0.7828 78.28%
CYP2D6 substrate - 0.7458 74.58%
CYP3A4 inhibition - 0.8310 83.10%
CYP2C9 inhibition - 0.7733 77.33%
CYP2C19 inhibition - 0.7802 78.02%
CYP2D6 inhibition - 0.9580 95.80%
CYP1A2 inhibition - 0.6544 65.44%
CYP2C8 inhibition - 0.6013 60.13%
CYP inhibitory promiscuity - 0.8224 82.24%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6172 61.72%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9404 94.04%
Skin irritation + 0.5471 54.71%
Skin corrosion - 0.9411 94.11%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6581 65.81%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.5865 58.65%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.8214 82.14%
Acute Oral Toxicity (c) III 0.5473 54.73%
Estrogen receptor binding + 0.8246 82.46%
Androgen receptor binding + 0.7132 71.32%
Thyroid receptor binding + 0.6375 63.75%
Glucocorticoid receptor binding + 0.7423 74.23%
Aromatase binding + 0.6900 69.00%
PPAR gamma + 0.5649 56.49%
Honey bee toxicity - 0.6942 69.42%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9867 98.67%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.63% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.42% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.27% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.32% 98.95%
CHEMBL284 P27487 Dipeptidyl peptidase IV 90.04% 95.69%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 89.13% 92.86%
CHEMBL218 P21554 Cannabinoid CB1 receptor 88.34% 96.61%
CHEMBL2996 Q05655 Protein kinase C delta 87.04% 97.79%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 86.23% 91.03%
CHEMBL4227 P25090 Lipoxin A4 receptor 85.94% 100.00%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 85.88% 95.58%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 85.82% 92.88%
CHEMBL236 P41143 Delta opioid receptor 85.77% 99.35%
CHEMBL2179 P04062 Beta-glucocerebrosidase 85.38% 85.31%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.33% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.05% 95.89%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 84.78% 98.75%
CHEMBL233 P35372 Mu opioid receptor 84.08% 97.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.81% 97.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.54% 97.29%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.34% 93.56%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.18% 97.14%
CHEMBL1977 P11473 Vitamin D receptor 82.80% 99.43%
CHEMBL1741186 P51449 Nuclear receptor ROR-gamma 82.68% 99.17%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.07% 99.18%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.78% 93.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.49% 100.00%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 80.42% 100.00%

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.
Plumbago zeylanica
Xylopia columbiana

Cross-Links

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PubChem 11453918
NPASS NPC59462
LOTUS LTS0015062
wikiData Q105133608