Nimbilin

Details

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Internal ID 64fac799-dd4b-4dfb-a27a-97b0364e0507
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name [17-acetyloxy-8-(furan-3-yl)-4-hydroxy-1,9,11,16-tetramethyl-12-[(E)-3-phenylprop-2-enoyl]oxy-5,14-dioxapentacyclo[11.6.1.02,11.06,10.016,20]icos-9-en-19-yl] (E)-2-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H50O10/c1-8-23(2)39(46)51-32-20-31(49-25(4)43)40(5)22-48-36-37(40)41(32,6)30-19-34(45)50-29-18-28(27-16-17-47-21-27)24(3)35(29)42(30,7)38(36)52-33(44)15-14-26-12-10-9-11-13-26/h8-17,21,28-32,34,36-38,45H,18-20,22H2,1-7H3/b15-14+,23-8+
InChI Key NTNUMTAFBRLDAX-RJYQGEKKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C42H50O10
Molecular Weight 714.80 g/mol
Exact Mass 714.34039779 g/mol
Topological Polar Surface Area (TPSA) 131.00 Ų
XlogP 5.90
Atomic LogP (AlogP) 6.69
H-Bond Acceptor 10
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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126617-60-5

2D Structure

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2D Structure of Nimbilin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 - 0.8244 82.44%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.7908 79.08%
OATP2B1 inhibitior - 0.5741 57.41%
OATP1B1 inhibitior + 0.7666 76.66%
OATP1B3 inhibitior + 0.9093 90.93%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 1.0000 100.00%
P-glycoprotein inhibitior + 0.8518 85.18%
P-glycoprotein substrate + 0.6762 67.62%
CYP3A4 substrate + 0.7239 72.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8903 89.03%
CYP3A4 inhibition + 0.5094 50.94%
CYP2C9 inhibition - 0.7680 76.80%
CYP2C19 inhibition - 0.8390 83.90%
CYP2D6 inhibition - 0.9409 94.09%
CYP1A2 inhibition - 0.8115 81.15%
CYP2C8 inhibition + 0.8732 87.32%
CYP inhibitory promiscuity - 0.8324 83.24%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Danger 0.4334 43.34%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.9138 91.38%
Skin irritation - 0.5930 59.30%
Skin corrosion - 0.9430 94.30%
Ames mutagenesis - 0.5978 59.78%
Human Ether-a-go-go-Related Gene inhibition + 0.8227 82.27%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.6209 62.09%
skin sensitisation - 0.8626 86.26%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.6226 62.26%
Acute Oral Toxicity (c) I 0.6682 66.82%
Estrogen receptor binding + 0.8334 83.34%
Androgen receptor binding + 0.7455 74.55%
Thyroid receptor binding + 0.6200 62.00%
Glucocorticoid receptor binding + 0.8206 82.06%
Aromatase binding + 0.6348 63.48%
PPAR gamma + 0.8100 81.00%
Honey bee toxicity - 0.6201 62.01%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.95% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 98.69% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 98.32% 90.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 97.18% 95.50%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 96.67% 81.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.23% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.13% 97.09%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 93.76% 89.44%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.72% 96.09%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 93.33% 93.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.63% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.75% 89.00%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 90.76% 87.67%
CHEMBL4302 P08183 P-glycoprotein 1 89.86% 92.98%
CHEMBL2581 P07339 Cathepsin D 88.32% 98.95%
CHEMBL3714130 P46095 G-protein coupled receptor 6 88.22% 97.36%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.01% 99.23%
CHEMBL5028 O14672 ADAM10 86.58% 97.50%
CHEMBL3401 O75469 Pregnane X receptor 84.46% 94.73%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 83.82% 83.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.12% 97.14%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.81% 96.25%

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.
Azadirachta indica

Cross-Links

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PubChem 6442484
LOTUS LTS0170549
wikiData Q105185551