Microporenic acid C

Details

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Internal ID 6f4dd578-32c9-42b6-868a-e4873ff63550
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name (1R,2S)-1-[(2E,6E,10E,14E)-15-carboxy-3,7,11-trimethylhexadeca-2,6,10,14-tetraenoxy]propane-1,2,3-tricarboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H38O9/c1-17(8-5-9-18(2)12-7-13-20(4)24(29)30)10-6-11-19(3)14-15-35-23(26(33)34)21(25(31)32)16-22(27)28/h9-10,13-14,21,23H,5-8,11-12,15-16H2,1-4H3,(H,27,28)(H,29,30)(H,31,32)(H,33,34)/b17-10+,18-9+,19-14+,20-13+/t21-,23+/m0/s1
InChI Key GGBZDYXEXJJNIW-NQGSRCNPSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C26H38O9
Molecular Weight 494.60 g/mol
Exact Mass 494.25158279 g/mol
Topological Polar Surface Area (TPSA) 158.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.84
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 18

Synonyms

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CHEMBL4283521

2D Structure

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2D Structure of Microporenic acid C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9205 92.05%
Caco-2 - 0.8020 80.20%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8185 81.85%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8920 89.20%
OATP1B3 inhibitior + 0.9482 94.82%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7911 79.11%
P-glycoprotein inhibitior + 0.6888 68.88%
P-glycoprotein substrate - 0.8741 87.41%
CYP3A4 substrate + 0.5164 51.64%
CYP2C9 substrate + 0.8217 82.17%
CYP2D6 substrate - 0.9150 91.50%
CYP3A4 inhibition - 0.6865 68.65%
CYP2C9 inhibition - 0.8403 84.03%
CYP2C19 inhibition - 0.8576 85.76%
CYP2D6 inhibition - 0.9013 90.13%
CYP1A2 inhibition - 0.7717 77.17%
CYP2C8 inhibition - 0.8120 81.20%
CYP inhibitory promiscuity - 0.9186 91.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.6863 68.63%
Eye corrosion - 0.9426 94.26%
Eye irritation - 0.8811 88.11%
Skin irritation - 0.7465 74.65%
Skin corrosion - 0.9874 98.74%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6954 69.54%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8720 87.20%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.8561 85.61%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.6812 68.12%
Acute Oral Toxicity (c) IV 0.6176 61.76%
Estrogen receptor binding + 0.6592 65.92%
Androgen receptor binding + 0.5573 55.73%
Thyroid receptor binding + 0.5436 54.36%
Glucocorticoid receptor binding + 0.6351 63.51%
Aromatase binding + 0.5288 52.88%
PPAR gamma + 0.6132 61.32%
Honey bee toxicity - 0.8591 85.91%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6255 62.55%
Fish aquatic toxicity + 0.9623 96.23%

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
CHEMBL2581 P07339 Cathepsin D 95.09% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.97% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.46% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.17% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 82.53% 94.73%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.90% 93.00%
CHEMBL340 P08684 Cytochrome P450 3A4 80.17% 91.19%

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 139589919
LOTUS LTS0027837
wikiData Q105007948