CID 73154136

Details

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Internal ID 3ce3c94e-9e29-4265-8b4c-d82889b66773
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Oxosteroids > 19-oxosteroids
IUPAC Name 7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.02,11.05,10.016,24.017,22]tetracosa-16(24),17,19,21-tetraene-10-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H37NO3/c1-25(2,31)22-12-14-28(16-30)21-10-9-17-15-19-18-7-5-6-8-20(18)29-24(19)27(17,4)26(21,3)13-11-23(28)32-22/h5-8,16-17,21-23,29,31H,9-15H2,1-4H3
InChI Key AYNSNFZADBZRGD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H37NO3
Molecular Weight 435.60 g/mol
Exact Mass 435.27734404 g/mol
Topological Polar Surface Area (TPSA) 62.30 Ų
XlogP 4.90
Atomic LogP (AlogP) 5.31
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 73154136

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9889 98.89%
Caco-2 - 0.5598 55.98%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6994 69.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8327 83.27%
OATP1B3 inhibitior + 0.9335 93.35%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9910 99.10%
P-glycoprotein inhibitior + 0.6413 64.13%
P-glycoprotein substrate - 0.5093 50.93%
CYP3A4 substrate + 0.6864 68.64%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.7208 72.08%
CYP3A4 inhibition - 0.8729 87.29%
CYP2C9 inhibition - 0.8722 87.22%
CYP2C19 inhibition - 0.7882 78.82%
CYP2D6 inhibition - 0.9147 91.47%
CYP1A2 inhibition + 0.5896 58.96%
CYP2C8 inhibition + 0.7506 75.06%
CYP inhibitory promiscuity - 0.6441 64.41%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6214 62.14%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9780 97.80%
Skin irritation - 0.7769 77.69%
Skin corrosion - 0.9377 93.77%
Ames mutagenesis - 0.6008 60.08%
Human Ether-a-go-go-Related Gene inhibition + 0.8277 82.77%
Micronuclear - 0.6400 64.00%
Hepatotoxicity - 0.6216 62.16%
skin sensitisation - 0.8173 81.73%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.5725 57.25%
Acute Oral Toxicity (c) III 0.5608 56.08%
Estrogen receptor binding + 0.9172 91.72%
Androgen receptor binding + 0.6679 66.79%
Thyroid receptor binding + 0.7416 74.16%
Glucocorticoid receptor binding + 0.8401 84.01%
Aromatase binding + 0.8102 81.02%
PPAR gamma + 0.6191 61.91%
Honey bee toxicity - 0.8477 84.77%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9445 94.45%

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 99.02% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 98.06% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.55% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.09% 89.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 89.31% 95.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.68% 97.09%
CHEMBL3310 Q96DB2 Histone deacetylase 11 88.42% 88.56%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 88.20% 94.23%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 86.59% 96.39%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.01% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.38% 96.09%
CHEMBL5028 O14672 ADAM10 85.07% 97.50%
CHEMBL2581 P07339 Cathepsin D 85.03% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.00% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.47% 92.62%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.32% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.31% 100.00%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 82.60% 95.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.51% 94.00%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.08% 94.62%
CHEMBL1937 Q92769 Histone deacetylase 2 81.21% 94.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 73154136
LOTUS LTS0213739
wikiData Q77279693