Cladosporiumin C

Details

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Internal ID c328ba81-1cd4-4980-9038-5f95b7a33c0c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name (3S)-3-[(E)-5-hydroxyhex-2-enyl]-3-[(2R,4R)-2-methyl-6-oxooxan-4-yl]-5-propan-2-ylidenepyrrolidine-2,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H27NO5/c1-11(2)16-17(23)19(18(24)20-16,8-6-5-7-12(3)21)14-9-13(4)25-15(22)10-14/h5-6,12-14,21H,7-10H2,1-4H3,(H,20,24)/b6-5+/t12?,13-,14-,19+/m1/s1
InChI Key IIYKLCYWWXLYAF-KOGDREQUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H27NO5
Molecular Weight 349.40 g/mol
Exact Mass 349.18892296 g/mol
Topological Polar Surface Area (TPSA) 92.70 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.02
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cladosporiumin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9089 90.89%
Caco-2 - 0.5807 58.07%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7614 76.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8649 86.49%
OATP1B3 inhibitior + 0.9274 92.74%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5833 58.33%
P-glycoprotein inhibitior - 0.8070 80.70%
P-glycoprotein substrate - 0.6626 66.26%
CYP3A4 substrate + 0.5588 55.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9060 90.60%
CYP3A4 inhibition - 0.9239 92.39%
CYP2C9 inhibition - 0.8031 80.31%
CYP2C19 inhibition - 0.8107 81.07%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition - 0.8890 88.90%
CYP2C8 inhibition - 0.8097 80.97%
CYP inhibitory promiscuity - 0.7781 77.81%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5006 50.06%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9896 98.96%
Skin irritation - 0.7437 74.37%
Skin corrosion - 0.9158 91.58%
Ames mutagenesis - 0.5454 54.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5522 55.22%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8111 81.11%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.5984 59.84%
Acute Oral Toxicity (c) III 0.4459 44.59%
Estrogen receptor binding + 0.5578 55.78%
Androgen receptor binding - 0.6316 63.16%
Thyroid receptor binding - 0.4933 49.33%
Glucocorticoid receptor binding + 0.7189 71.89%
Aromatase binding + 0.6492 64.92%
PPAR gamma + 0.5509 55.09%
Honey bee toxicity - 0.8359 83.59%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8860 88.60%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.82% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.04% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.78% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.53% 91.11%
CHEMBL299 P17252 Protein kinase C alpha 93.45% 98.03%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.04% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.65% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.59% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.84% 95.56%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 87.87% 95.58%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.22% 89.34%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.87% 99.23%
CHEMBL2996 Q05655 Protein kinase C delta 86.45% 97.79%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.36% 89.00%
CHEMBL325 Q13547 Histone deacetylase 1 82.55% 95.92%
CHEMBL3401 O75469 Pregnane X receptor 82.50% 94.73%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.61% 90.08%
CHEMBL1951 P21397 Monoamine oxidase A 81.52% 91.49%
CHEMBL213 P08588 Beta-1 adrenergic receptor 81.12% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.05% 93.56%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 80.62% 85.11%
CHEMBL1937 Q92769 Histone deacetylase 2 80.41% 94.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 139590259
LOTUS LTS0261753
wikiData Q105113829