Pitholide D

Details

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Internal ID 1208ba91-2958-4ef3-8aed-0060f7a5c348
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Annonaceous acetogenins
IUPAC Name (9R,9aS)-9-hydroxy-6,9a-dimethyl-3-octanoyl-9H-furo[3,2-g]isochromen-2-one
SMILES (Canonical) CCCCCCCC(=O)C1=C2C=C3C=C(OC=C3C(C2(OC1=O)C)O)C
SMILES (Isomeric) CCCCCCCC(=O)C1=C2C=C3C=C(OC=C3[C@H]([C@]2(OC1=O)C)O)C
InChI InChI=1S/C21H26O5/c1-4-5-6-7-8-9-17(22)18-16-11-14-10-13(2)25-12-15(14)19(23)21(16,3)26-20(18)24/h10-12,19,23H,4-9H2,1-3H3/t19-,21+/m1/s1
InChI Key LWWKRRPNDFSENZ-CTNGQTDRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H26O5
Molecular Weight 358.40 g/mol
Exact Mass 358.17802393 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.65
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pitholide D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 + 0.7274 72.74%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7369 73.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7423 74.23%
OATP1B3 inhibitior + 0.9070 90.70%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.7398 73.98%
P-glycoprotein inhibitior - 0.5246 52.46%
P-glycoprotein substrate - 0.6144 61.44%
CYP3A4 substrate + 0.6486 64.86%
CYP2C9 substrate - 0.7974 79.74%
CYP2D6 substrate - 0.8837 88.37%
CYP3A4 inhibition - 0.5341 53.41%
CYP2C9 inhibition - 0.9342 93.42%
CYP2C19 inhibition - 0.9355 93.55%
CYP2D6 inhibition - 0.9518 95.18%
CYP1A2 inhibition - 0.8125 81.25%
CYP2C8 inhibition + 0.4613 46.13%
CYP inhibitory promiscuity - 0.9214 92.14%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Danger 0.4166 41.66%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9190 91.90%
Skin irritation + 0.6727 67.27%
Skin corrosion - 0.8751 87.51%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5569 55.69%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.5327 53.27%
skin sensitisation - 0.8522 85.22%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.5574 55.74%
Acute Oral Toxicity (c) III 0.5282 52.82%
Estrogen receptor binding + 0.7561 75.61%
Androgen receptor binding + 0.6173 61.73%
Thyroid receptor binding + 0.5332 53.32%
Glucocorticoid receptor binding + 0.7702 77.02%
Aromatase binding + 0.6539 65.39%
PPAR gamma + 0.5968 59.68%
Honey bee toxicity - 0.9096 90.96%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6528 65.28%
Fish aquatic toxicity + 0.9895 98.95%

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
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 96.40% 85.94%
CHEMBL2581 P07339 Cathepsin D 95.82% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.46% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.14% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.52% 99.17%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 91.71% 95.17%
CHEMBL299 P17252 Protein kinase C alpha 91.32% 98.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.20% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.13% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.95% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.76% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 89.28% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 89.02% 89.63%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.42% 89.00%
CHEMBL2996 Q05655 Protein kinase C delta 83.11% 97.79%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.43% 93.99%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.47% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 80.52% 90.17%

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 21774811
LOTUS LTS0030182
wikiData Q77310638