Asperversin D

Details

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Internal ID b5bc18b6-c5d6-4797-a65f-099a7b0da564
Taxonomy Organoheterocyclic compounds > Lactones
IUPAC Name (1R,2S,3S,8R,11R)-3-hydroxy-2,7,7,11,15-pentamethyl-6,12,16-trioxatetracyclo[9.8.0.02,8.013,18]nonadeca-13(18),14-diene-5,17-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H28O6/c1-11-8-13-12(18(24)25-11)9-15-20(4,26-13)7-6-14-19(2,3)27-17(23)10-16(22)21(14,15)5/h8,14-16,22H,6-7,9-10H2,1-5H3/t14-,15-,16-,20+,21-/m0/s1
InChI Key JZUWHWXBAGVOIA-CPSBXNMUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H28O6
Molecular Weight 376.40 g/mol
Exact Mass 376.18858861 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.76
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Asperversin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9639 96.39%
Caco-2 + 0.6515 65.15%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7692 76.92%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9027 90.27%
OATP1B3 inhibitior + 0.8681 86.81%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7666 76.66%
P-glycoprotein inhibitior - 0.5791 57.91%
P-glycoprotein substrate - 0.7311 73.11%
CYP3A4 substrate + 0.6458 64.58%
CYP2C9 substrate - 0.5684 56.84%
CYP2D6 substrate - 0.8462 84.62%
CYP3A4 inhibition - 0.8032 80.32%
CYP2C9 inhibition - 0.8661 86.61%
CYP2C19 inhibition - 0.8989 89.89%
CYP2D6 inhibition - 0.9474 94.74%
CYP1A2 inhibition - 0.6821 68.21%
CYP2C8 inhibition - 0.6014 60.14%
CYP inhibitory promiscuity - 0.9863 98.63%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6955 69.55%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.8316 83.16%
Skin irritation - 0.6408 64.08%
Skin corrosion - 0.9025 90.25%
Ames mutagenesis - 0.7564 75.64%
Human Ether-a-go-go-Related Gene inhibition - 0.4013 40.13%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8733 87.33%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6145 61.45%
Acute Oral Toxicity (c) III 0.4556 45.56%
Estrogen receptor binding + 0.8047 80.47%
Androgen receptor binding + 0.6306 63.06%
Thyroid receptor binding - 0.5200 52.00%
Glucocorticoid receptor binding + 0.7998 79.98%
Aromatase binding + 0.5422 54.22%
PPAR gamma + 0.6877 68.77%
Honey bee toxicity - 0.8425 84.25%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9898 98.98%

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 97.34% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.43% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.85% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.12% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.03% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.74% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.37% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.50% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.29% 93.04%
CHEMBL1871 P10275 Androgen Receptor 83.17% 96.43%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.29% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.68% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.13% 94.80%

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 139590628
LOTUS LTS0156569
wikiData Q105137608