(17beta,20r,22e,24r)-19-Norergosta-1,3,5,7,9,14,22-heptaene

Details

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Internal ID 146914dc-5767-4cee-907d-c762737406a1
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cholestane steroids
IUPAC Name (13R,17R)-17-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-13-methyl-11,12,16,17-tetrahydrocyclopenta[a]phenanthrene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H34/c1-18(2)19(3)10-11-20(4)25-14-15-26-24-13-12-21-8-6-7-9-22(21)23(24)16-17-27(25,26)5/h6-13,15,18-20,25H,14,16-17H2,1-5H3/b11-10+/t19-,20-,25-,27-/m1/s1
InChI Key DBRICIKZTYJLQL-HXDDMZSUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H34
Molecular Weight 358.60 g/mol
Exact Mass 358.266051085 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 8.20
Atomic LogP (AlogP) 7.68
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (17beta,20r,22e,24r)-19-Norergosta-1,3,5,7,9,14,22-heptaene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.7577 75.77%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.5100 51.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9020 90.20%
OATP1B3 inhibitior + 0.9242 92.42%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.9753 97.53%
P-glycoprotein inhibitior + 0.8792 87.92%
P-glycoprotein substrate - 0.6579 65.79%
CYP3A4 substrate + 0.6463 64.63%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.7261 72.61%
CYP3A4 inhibition - 0.7916 79.16%
CYP2C9 inhibition - 0.6697 66.97%
CYP2C19 inhibition + 0.6909 69.09%
CYP2D6 inhibition - 0.8668 86.68%
CYP1A2 inhibition - 0.6559 65.59%
CYP2C8 inhibition + 0.5122 51.22%
CYP inhibitory promiscuity + 0.7577 75.77%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.4726 47.26%
Eye corrosion - 0.9856 98.56%
Eye irritation - 0.9858 98.58%
Skin irritation - 0.6943 69.43%
Skin corrosion - 0.9622 96.22%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9384 93.84%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5334 53.34%
skin sensitisation + 0.6729 67.29%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.5530 55.30%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.7777 77.77%
Acute Oral Toxicity (c) III 0.5446 54.46%
Estrogen receptor binding + 0.8620 86.20%
Androgen receptor binding + 0.6532 65.32%
Thyroid receptor binding + 0.8001 80.01%
Glucocorticoid receptor binding + 0.5421 54.21%
Aromatase binding + 0.5591 55.91%
PPAR gamma + 0.7269 72.69%
Honey bee toxicity - 0.8092 80.92%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 1.0000 100.00%

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 98.30% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.90% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.61% 95.56%
CHEMBL240 Q12809 HERG 94.44% 89.76%
CHEMBL3359 P21462 Formyl peptide receptor 1 90.20% 93.56%
CHEMBL221 P23219 Cyclooxygenase-1 89.00% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.76% 97.25%
CHEMBL2535 P11166 Glucose transporter 88.35% 98.75%
CHEMBL1907 P15144 Aminopeptidase N 88.24% 93.31%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.99% 82.69%
CHEMBL1937 Q92769 Histone deacetylase 2 87.20% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.11% 97.09%
CHEMBL4072 P07858 Cathepsin B 85.73% 93.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.49% 96.09%
CHEMBL3869 P50281 Matrix metalloproteinase 14 85.37% 93.10%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.23% 96.67%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 82.90% 85.94%
CHEMBL5600 P27448 Serine/threonine-protein kinase c-TAK1 82.84% 88.81%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 82.48% 95.00%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 82.20% 85.11%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 80.95% 95.83%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.82% 100.00%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.65% 93.81%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.32% 100.00%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.04% 96.25%

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 21574238
LOTUS LTS0168805
wikiData Q105380458