FR171456

Details

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Internal ID 2a3088bd-43d7-494b-8294-964749f7d568
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name 6,11,18-trihydroxy-7,16-dimethyl-15-(6-methyl-5-methylideneheptan-2-yl)-4,9-dioxopentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H44O7/c1-15(2)16(3)7-8-17(4)18-9-10-20-26(18,5)13-23(34)29-14-28(29)22(33)11-21(32)27(6,25(35)36)24(28)19(31)12-30(20,29)37/h15,17-18,20-21,23-24,32,34,37H,3,7-14H2,1-2,4-6H3,(H,35,36)
InChI Key JAHGNOXPMXOEJS-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C30H44O7
Molecular Weight 516.70 g/mol
Exact Mass 516.30870374 g/mol
Topological Polar Surface Area (TPSA) 132.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.53
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of FR171456

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9787 97.87%
Caco-2 - 0.6986 69.86%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6892 68.92%
OATP2B1 inhibitior - 0.5662 56.62%
OATP1B1 inhibitior + 0.8743 87.43%
OATP1B3 inhibitior - 0.2978 29.78%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7782 77.82%
BSEP inhibitior + 0.5892 58.92%
P-glycoprotein inhibitior - 0.4820 48.20%
P-glycoprotein substrate + 0.6682 66.82%
CYP3A4 substrate + 0.6843 68.43%
CYP2C9 substrate - 0.8274 82.74%
CYP2D6 substrate - 0.8602 86.02%
CYP3A4 inhibition - 0.7714 77.14%
CYP2C9 inhibition - 0.6780 67.80%
CYP2C19 inhibition - 0.8642 86.42%
CYP2D6 inhibition - 0.9533 95.33%
CYP1A2 inhibition - 0.8869 88.69%
CYP2C8 inhibition - 0.6026 60.26%
CYP inhibitory promiscuity - 0.8789 87.89%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7043 70.43%
Eye corrosion - 0.9922 99.22%
Eye irritation - 0.9193 91.93%
Skin irritation + 0.5647 56.47%
Skin corrosion - 0.9341 93.41%
Ames mutagenesis - 0.6937 69.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5852 58.52%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5086 50.86%
skin sensitisation - 0.7234 72.34%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity + 0.7303 73.03%
Acute Oral Toxicity (c) I 0.6903 69.03%
Estrogen receptor binding + 0.7440 74.40%
Androgen receptor binding + 0.7764 77.64%
Thyroid receptor binding + 0.5680 56.80%
Glucocorticoid receptor binding + 0.7387 73.87%
Aromatase binding + 0.7344 73.44%
PPAR gamma + 0.5682 56.82%
Honey bee toxicity - 0.8343 83.43%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6700 67.00%
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
CHEMBL2581 P07339 Cathepsin D 97.41% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.23% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.05% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.13% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.27% 94.45%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 90.67% 93.00%
CHEMBL3524 P56524 Histone deacetylase 4 90.20% 92.97%
CHEMBL340 P08684 Cytochrome P450 3A4 87.62% 91.19%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.68% 90.71%
CHEMBL220 P22303 Acetylcholinesterase 85.70% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.56% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.26% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.78% 92.62%
CHEMBL221 P23219 Cyclooxygenase-1 82.56% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.64% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.23% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 81.01% 94.75%
CHEMBL237 P41145 Kappa opioid receptor 81.00% 98.10%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.75% 95.17%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.69% 96.47%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.28% 90.08%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.08% 93.04%

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 9827906
LOTUS LTS0121449
wikiData Q104169320