Salvixalapadiene

Details

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Internal ID fcc937b7-7525-47d4-93c2-110c90c5973f
Taxonomy Organoheterocyclic compounds > Isocoumarans > Isobenzofuranones > Phthalides
IUPAC Name 4-[(1R)-1-[(2R)-4-ethenyl-2-(furan-3-yl)-5-oxo-2H-furan-3-yl]ethyl]-3H-2-benzofuran-1-one
SMILES (Canonical) CC(C1=CC=CC2=C1COC2=O)C3=C(C(=O)OC3C4=COC=C4)C=C
SMILES (Isomeric) C[C@H](C1=CC=CC2=C1COC2=O)C3=C(C(=O)O[C@H]3C4=COC=C4)C=C
InChI InChI=1S/C20H16O5/c1-3-13-17(18(25-20(13)22)12-7-8-23-9-12)11(2)14-5-4-6-15-16(14)10-24-19(15)21/h3-9,11,18H,1,10H2,2H3/t11-,18+/m1/s1
InChI Key SOQMKYUDTQPTRT-ZMZPIMSZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H16O5
Molecular Weight 336.30 g/mol
Exact Mass 336.09977361 g/mol
Topological Polar Surface Area (TPSA) 65.70 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.83
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Salvixalapadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 - 0.5493 54.93%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7648 76.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8593 85.93%
OATP1B3 inhibitior + 0.9483 94.83%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7622 76.22%
P-glycoprotein inhibitior - 0.5258 52.58%
P-glycoprotein substrate - 0.6916 69.16%
CYP3A4 substrate + 0.6049 60.49%
CYP2C9 substrate - 0.7924 79.24%
CYP2D6 substrate - 0.8876 88.76%
CYP3A4 inhibition - 0.8445 84.45%
CYP2C9 inhibition + 0.7656 76.56%
CYP2C19 inhibition + 0.6464 64.64%
CYP2D6 inhibition - 0.9381 93.81%
CYP1A2 inhibition + 0.8052 80.52%
CYP2C8 inhibition - 0.7144 71.44%
CYP inhibitory promiscuity + 0.6426 64.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9143 91.43%
Carcinogenicity (trinary) Non-required 0.6030 60.30%
Eye corrosion - 0.9679 96.79%
Eye irritation - 0.9594 95.94%
Skin irritation - 0.6689 66.89%
Skin corrosion - 0.9275 92.75%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8277 82.77%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.5817 58.17%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.4852 48.52%
Acute Oral Toxicity (c) III 0.4807 48.07%
Estrogen receptor binding + 0.7676 76.76%
Androgen receptor binding + 0.6458 64.58%
Thyroid receptor binding - 0.6115 61.15%
Glucocorticoid receptor binding + 0.7484 74.84%
Aromatase binding + 0.5284 52.84%
PPAR gamma + 0.7044 70.44%
Honey bee toxicity - 0.7398 73.98%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9967 99.67%

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
CHEMBL1951 P21397 Monoamine oxidase A 99.45% 91.49%
CHEMBL2039 P27338 Monoamine oxidase B 97.42% 92.51%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.04% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.71% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.97% 97.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 89.62% 96.47%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.86% 89.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.41% 97.25%
CHEMBL1929 P47989 Xanthine dehydrogenase 87.72% 96.12%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.04% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.04% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 86.31% 93.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.31% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 86.22% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.99% 100.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.62% 93.40%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.10% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.06% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.87% 94.45%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.81% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.84% 93.56%

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.
Salvia xalapensis

Cross-Links

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PubChem 11348272
LOTUS LTS0096863
wikiData Q105257113