Pretrichodermamide D

Details

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Internal ID baa96560-8a20-48b2-87e5-d45633951e05
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name (1R,3S,6R,7R,8S,12S,13S)-3,6,7-trihydroxy-13-(2-hydroxy-3,4-dimethoxyphenyl)-17-methyl-9-oxa-14,15-dithia-10,17-diazatetracyclo[10.3.2.01,10.03,8]heptadec-4-ene-11,16-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H24N2O9S2/c1-22-12-16(9-4-5-11(30-2)15(31-3)13(9)25)33-34-21(19(22)28)8-20(29)7-6-10(24)14(26)17(20)32-23(21)18(12)27/h4-7,10,12,14,16-17,24-26,29H,8H2,1-3H3/t10-,12-,14-,16+,17+,20-,21-/m1/s1
InChI Key PURMOBRKHQNGMM-OAWXJWLCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H24N2O9S2
Molecular Weight 512.60 g/mol
Exact Mass 512.09232269 g/mol
Topological Polar Surface Area (TPSA) 200.00 Ų
XlogP -1.00
Atomic LogP (AlogP) -0.06
H-Bond Acceptor 11
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pretrichodermamide D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5751 57.51%
Caco-2 - 0.7748 77.48%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.3885 38.85%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8775 87.75%
OATP1B3 inhibitior + 0.9382 93.82%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7471 74.71%
P-glycoprotein inhibitior - 0.4620 46.20%
P-glycoprotein substrate + 0.5747 57.47%
CYP3A4 substrate + 0.7095 70.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8130 81.30%
CYP3A4 inhibition + 0.7540 75.40%
CYP2C9 inhibition - 0.6679 66.79%
CYP2C19 inhibition - 0.6309 63.09%
CYP2D6 inhibition - 0.8627 86.27%
CYP1A2 inhibition - 0.7197 71.97%
CYP2C8 inhibition + 0.4587 45.87%
CYP inhibitory promiscuity - 0.7614 76.14%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5360 53.60%
Eye corrosion - 0.9783 97.83%
Eye irritation - 0.9552 95.52%
Skin irritation - 0.7602 76.02%
Skin corrosion - 0.9153 91.53%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6121 61.21%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8265 82.65%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6456 64.56%
Acute Oral Toxicity (c) III 0.5601 56.01%
Estrogen receptor binding + 0.8058 80.58%
Androgen receptor binding + 0.7400 74.00%
Thyroid receptor binding + 0.6347 63.47%
Glucocorticoid receptor binding + 0.7616 76.16%
Aromatase binding + 0.5529 55.29%
PPAR gamma + 0.6101 61.01%
Honey bee toxicity - 0.8118 81.18%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.8759 87.59%

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 98.12% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.02% 85.14%
CHEMBL2581 P07339 Cathepsin D 95.88% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.23% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.97% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.51% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.91% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.66% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.97% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.92% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.62% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.40% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.64% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.00% 97.25%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.93% 93.40%
CHEMBL2056 P21728 Dopamine D1 receptor 84.55% 91.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 84.19% 97.33%
CHEMBL217 P14416 Dopamine D2 receptor 84.06% 95.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.92% 96.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.27% 100.00%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 82.27% 82.38%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.17% 90.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.30% 92.62%

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 139590375
LOTUS LTS0159124
wikiData Q105215243