Fendlerinine C

Details

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Internal ID 2a51fb3f-1c27-4c96-8a64-816ba40479c2
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Glutamic acid and derivatives
IUPAC Name 2-[4-[[(1S,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]-7-carboxy-6-methoxy-5-methyl-3-oxo-1H-isoindol-2-yl]pentanedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H43NO10/c1-16-24(41-6)23(28(38)39)17-14-32(18(27(36)37)8-9-21(33)34)26(35)22(17)25(16)42-15-20-30(4)12-7-11-29(2,3)19(30)10-13-31(20,5)40/h18-20,40H,7-15H2,1-6H3,(H,33,34)(H,36,37)(H,38,39)/t18?,19-,20+,30-,31+/m0/s1
InChI Key XEJKXOPDHNLWQT-VJYBYOHASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H43NO10
Molecular Weight 589.70 g/mol
Exact Mass 589.28869657 g/mol
Topological Polar Surface Area (TPSA) 171.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.35
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Fendlerinine C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9268 92.68%
Caco-2 - 0.7618 76.18%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7629 76.29%
OATP2B1 inhibitior - 0.5698 56.98%
OATP1B1 inhibitior + 0.8151 81.51%
OATP1B3 inhibitior + 0.9267 92.67%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8866 88.66%
P-glycoprotein inhibitior + 0.6688 66.88%
P-glycoprotein substrate - 0.5504 55.04%
CYP3A4 substrate + 0.7021 70.21%
CYP2C9 substrate - 0.5979 59.79%
CYP2D6 substrate - 0.8787 87.87%
CYP3A4 inhibition + 0.5607 56.07%
CYP2C9 inhibition - 0.7172 71.72%
CYP2C19 inhibition - 0.6011 60.11%
CYP2D6 inhibition - 0.9067 90.67%
CYP1A2 inhibition - 0.9165 91.65%
CYP2C8 inhibition + 0.6186 61.86%
CYP inhibitory promiscuity - 0.6368 63.68%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5608 56.08%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9075 90.75%
Skin irritation - 0.8048 80.48%
Skin corrosion - 0.9429 94.29%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6363 63.63%
Micronuclear + 0.6800 68.00%
Hepatotoxicity - 0.6351 63.51%
skin sensitisation - 0.9025 90.25%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.9174 91.74%
Acute Oral Toxicity (c) III 0.6245 62.45%
Estrogen receptor binding + 0.7584 75.84%
Androgen receptor binding + 0.6306 63.06%
Thyroid receptor binding - 0.5454 54.54%
Glucocorticoid receptor binding + 0.8002 80.02%
Aromatase binding + 0.7541 75.41%
PPAR gamma + 0.6397 63.97%
Honey bee toxicity - 0.7951 79.51%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9514 95.14%

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
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 99.63% 95.17%
CHEMBL4302 P08183 P-glycoprotein 1 98.69% 92.98%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.39% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.28% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.20% 94.45%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 97.06% 96.38%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 95.90% 93.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.62% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.75% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 90.97% 93.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 90.58% 96.47%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 89.02% 82.38%
CHEMBL4040 P28482 MAP kinase ERK2 88.87% 83.82%
CHEMBL340 P08684 Cytochrome P450 3A4 88.03% 91.19%
CHEMBL1871 P10275 Androgen Receptor 88.00% 96.43%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.60% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.38% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.78% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.71% 99.23%
CHEMBL5255 O00206 Toll-like receptor 4 83.60% 92.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.09% 95.89%
CHEMBL2535 P11166 Glucose transporter 82.98% 98.75%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 82.92% 95.34%
CHEMBL1907 P15144 Aminopeptidase N 81.79% 93.31%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.65% 100.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.32% 91.07%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.22% 89.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.66% 94.08%

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 139590817
LOTUS LTS0056353
wikiData Q105326384