Aperterpene N

Details

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Internal ID 22aa511b-5bc0-4538-bfba-f8b68ede2287
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Oxosteroids
IUPAC Name methyl (5R,8R,9R,10R,13S,14S,16R)-16-hydroxy-4,4,8,10,13,16-hexamethyl-12-methylidene-3,6,15,17-tetraoxo-1,2,5,7,9,11-hexahydrocyclopenta[a]phenanthrene-14-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H34O7/c1-13-11-15-22(4)10-9-16(28)21(2,3)17(22)14(27)12-23(15,5)26(20(31)33-8)19(30)25(7,32)18(29)24(13,26)6/h15,17,32H,1,9-12H2,2-8H3/t15-,17+,22-,23-,24-,25-,26+/m1/s1
InChI Key AAEFHLQEFDWSRN-LTUMHGGBSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C26H34O7
Molecular Weight 458.50 g/mol
Exact Mass 458.23045342 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.62
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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Aperterpene N
BDBM50591631

2D Structure

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2D Structure of Aperterpene N

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9888 98.88%
Caco-2 - 0.5666 56.66%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7750 77.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8784 87.84%
OATP1B3 inhibitior - 0.2622 26.22%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6900 69.00%
P-glycoprotein inhibitior - 0.4353 43.53%
P-glycoprotein substrate - 0.6660 66.60%
CYP3A4 substrate + 0.6497 64.97%
CYP2C9 substrate - 0.8185 81.85%
CYP2D6 substrate - 0.8749 87.49%
CYP3A4 inhibition - 0.7115 71.15%
CYP2C9 inhibition - 0.8318 83.18%
CYP2C19 inhibition - 0.8672 86.72%
CYP2D6 inhibition - 0.9620 96.20%
CYP1A2 inhibition - 0.7183 71.83%
CYP2C8 inhibition - 0.7080 70.80%
CYP inhibitory promiscuity - 0.9625 96.25%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9420 94.20%
Carcinogenicity (trinary) Non-required 0.6277 62.77%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.8300 83.00%
Skin irritation + 0.5339 53.39%
Skin corrosion - 0.9545 95.45%
Ames mutagenesis - 0.5528 55.28%
Human Ether-a-go-go-Related Gene inhibition + 0.6587 65.87%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.6541 65.41%
skin sensitisation - 0.7306 73.06%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.5643 56.43%
Acute Oral Toxicity (c) I 0.3943 39.43%
Estrogen receptor binding + 0.5947 59.47%
Androgen receptor binding + 0.7428 74.28%
Thyroid receptor binding + 0.6948 69.48%
Glucocorticoid receptor binding + 0.6558 65.58%
Aromatase binding + 0.7060 70.60%
PPAR gamma + 0.5752 57.52%
Honey bee toxicity - 0.8003 80.03%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9969 99.69%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.96% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.14% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.53% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 88.28% 91.19%
CHEMBL2581 P07339 Cathepsin D 88.05% 98.95%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.83% 93.03%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.57% 82.69%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.20% 85.30%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.12% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.04% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.05% 85.14%
CHEMBL5028 O14672 ADAM10 85.04% 97.50%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.22% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.18% 95.56%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.72% 97.50%

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 146682520
LOTUS LTS0183163
wikiData Q104907862