(1R,3S,4R,5S,7R,9S,12R,14S,17R,18R,19R,21R,22R)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosane-5,9-diol

Details

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Internal ID 2a0f17cd-090e-48d2-9026-267212cf5a3b
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cycloartanols and derivatives
IUPAC Name (1R,3S,4R,5S,7R,9S,12R,14S,17R,18R,19R,21R,22R)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosane-5,9-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H48O5/c1-16-12-18-23(25(4,5)33)35-30(34-18)14-27(7)22-17(31)13-19-24(2,3)20(32)8-9-28(19)15-29(22,28)11-10-26(27,6)21(16)30/h16-23,31-33H,8-15H2,1-7H3/t16-,17+,18-,19+,20+,21-,22-,23-,26-,27+,28-,29+,30-/m1/s1
InChI Key UIYLAWWWFYWOAN-ZDIAFKDISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48O5
Molecular Weight 488.70 g/mol
Exact Mass 488.35017463 g/mol
Topological Polar Surface Area (TPSA) 79.20 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.66
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,3S,4R,5S,7R,9S,12R,14S,17R,18R,19R,21R,22R)-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosane-5,9-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9373 93.73%
Caco-2 - 0.6457 64.57%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6168 61.68%
OATP2B1 inhibitior - 0.5767 57.67%
OATP1B1 inhibitior + 0.8580 85.80%
OATP1B3 inhibitior + 0.8238 82.38%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6821 68.21%
BSEP inhibitior - 0.6429 64.29%
P-glycoprotein inhibitior - 0.6543 65.43%
P-glycoprotein substrate - 0.6302 63.02%
CYP3A4 substrate + 0.6866 68.66%
CYP2C9 substrate - 0.8027 80.27%
CYP2D6 substrate - 0.7659 76.59%
CYP3A4 inhibition - 0.8782 87.82%
CYP2C9 inhibition - 0.8636 86.36%
CYP2C19 inhibition - 0.8463 84.63%
CYP2D6 inhibition - 0.9537 95.37%
CYP1A2 inhibition - 0.7414 74.14%
CYP2C8 inhibition + 0.5535 55.35%
CYP inhibitory promiscuity - 0.9676 96.76%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5495 54.95%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.9082 90.82%
Skin irritation - 0.5924 59.24%
Skin corrosion - 0.8958 89.58%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5847 58.47%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.5841 58.41%
skin sensitisation - 0.8448 84.48%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.7134 71.34%
Acute Oral Toxicity (c) I 0.3969 39.69%
Estrogen receptor binding + 0.6897 68.97%
Androgen receptor binding + 0.7351 73.51%
Thyroid receptor binding + 0.6143 61.43%
Glucocorticoid receptor binding + 0.6935 69.35%
Aromatase binding + 0.7609 76.09%
PPAR gamma + 0.6164 61.64%
Honey bee toxicity - 0.7574 75.74%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9185 91.85%

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 97.14% 97.25%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 93.76% 96.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.10% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.03% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.89% 96.77%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.39% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.05% 96.09%
CHEMBL259 P32245 Melanocortin receptor 4 85.99% 95.38%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 85.08% 100.00%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 84.97% 97.31%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.71% 82.69%
CHEMBL204 P00734 Thrombin 84.67% 96.01%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.33% 97.14%
CHEMBL1871 P10275 Androgen Receptor 83.63% 96.43%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.51% 95.50%
CHEMBL1977 P11473 Vitamin D receptor 83.24% 99.43%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.78% 89.00%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 82.50% 98.99%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.47% 92.94%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 82.43% 95.58%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.76% 91.03%
CHEMBL2996 Q05655 Protein kinase C delta 81.04% 97.79%
CHEMBL1902 P62942 FK506-binding protein 1A 80.27% 97.05%

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.
Astragalus orbiculatus

Cross-Links

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PubChem 162944418
LOTUS LTS0073198
wikiData Q105273741