Provincialin

Details

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Internal ID 67a6c3d5-f6b5-4a01-b739-5a025d33e42d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Germacranolides and derivatives
IUPAC Name [(3aR,4R,6E,9S,10Z,11aR)-9-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-[[(E)-2-(hydroxymethyl)but-2-enoyl]oxymethyl]but-2-enoate
SMILES (Canonical) CC=C(CO)C(=O)OCC(=CCO)C(=O)OC1CC(=CCC(C(=CC2C1C(=C)C(=O)O2)C)OC(=O)C)C
SMILES (Isomeric) C/C=C(\CO)/C(=O)OC/C(=C\CO)/C(=O)O[C@@H]1C/C(=C/C[C@@H](/C(=C\[C@@H]2[C@@H]1C(=C)C(=O)O2)/C)OC(=O)C)/C
InChI InChI=1S/C27H34O10/c1-6-19(13-29)26(32)34-14-20(9-10-28)27(33)37-22-11-15(2)7-8-21(35-18(5)30)16(3)12-23-24(22)17(4)25(31)36-23/h6-7,9,12,21-24,28-29H,4,8,10-11,13-14H2,1-3,5H3/b15-7+,16-12-,19-6+,20-9+/t21-,22+,23+,24+/m0/s1
InChI Key RQCXPCGOVWKZCE-UUFJRKJUSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H34O10
Molecular Weight 518.60 g/mol
Exact Mass 518.21519728 g/mol
Topological Polar Surface Area (TPSA) 146.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 2.01
H-Bond Acceptor 10
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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40328-96-9
C09533
CHEBI:8599
DTXSID001098155
[(3aR,4R,6E,9S,10Z,11aR)-9-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-[[(E)-2-(hydroxymethyl)but-2-enoyl]oxymethyl]but-2-enoate
Q27108106
2-Butenoic acid, 4-hydroxy-2-[[[(2E)-2-(hydroxymethyl)-1-oxo-2-buten-1-yl]oxy]methyl]-, (3aR,4R,6E,9S,10Z,11aR)-9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl ester, (2E)-

2D Structure

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2D Structure of Provincialin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9456 94.56%
Caco-2 - 0.7897 78.97%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6712 67.12%
OATP2B1 inhibitior - 0.8600 86.00%
OATP1B1 inhibitior + 0.8705 87.05%
OATP1B3 inhibitior + 0.9379 93.79%
MATE1 inhibitior - 0.8212 82.12%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9602 96.02%
P-glycoprotein inhibitior + 0.8050 80.50%
P-glycoprotein substrate + 0.5435 54.35%
CYP3A4 substrate + 0.6651 66.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9071 90.71%
CYP3A4 inhibition - 0.5067 50.67%
CYP2C9 inhibition - 0.8597 85.97%
CYP2C19 inhibition - 0.8075 80.75%
CYP2D6 inhibition - 0.9351 93.51%
CYP1A2 inhibition - 0.5855 58.55%
CYP2C8 inhibition + 0.5698 56.98%
CYP inhibitory promiscuity - 0.8648 86.48%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6317 63.17%
Eye corrosion - 0.9799 97.99%
Eye irritation - 0.9325 93.25%
Skin irritation - 0.6367 63.67%
Skin corrosion - 0.9475 94.75%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3910 39.10%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8547 85.47%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.7129 71.29%
Acute Oral Toxicity (c) III 0.4722 47.22%
Estrogen receptor binding + 0.7826 78.26%
Androgen receptor binding + 0.5689 56.89%
Thyroid receptor binding - 0.5241 52.41%
Glucocorticoid receptor binding + 0.7537 75.37%
Aromatase binding + 0.5784 57.84%
PPAR gamma + 0.5703 57.03%
Honey bee toxicity - 0.6816 68.16%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9883 98.83%

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 97.89% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.52% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 94.26% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.58% 86.33%
CHEMBL2581 P07339 Cathepsin D 87.48% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.27% 94.80%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.67% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.33% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.15% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.53% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.42% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 83.41% 97.79%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 80.90% 97.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.83% 93.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.46% 99.23%

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.
Ageratina cronquistii
Hymenopappus scabiosaeus
Mikania haenkeana

Cross-Links

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PubChem 5281494
LOTUS LTS0201781
wikiData Q27108106