Spiraformin C

Details

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Internal ID 64e9f60e-56e4-4b5a-b139-40950d2e0352
Taxonomy Benzenoids > Benzene and substituted derivatives > Diphenylethers
IUPAC Name butyl 3-[4-[2-hydroxy-5-[(E)-3-methoxy-3-oxoprop-1-enyl]phenoxy]phenyl]propanoate
SMILES (Canonical) CCCCOC(=O)CCC1=CC=C(C=C1)OC2=C(C=CC(=C2)C=CC(=O)OC)O
SMILES (Isomeric) CCCCOC(=O)CCC1=CC=C(C=C1)OC2=C(C=CC(=C2)/C=C/C(=O)OC)O
InChI InChI=1S/C23H26O6/c1-3-4-15-28-23(26)14-8-17-5-10-19(11-6-17)29-21-16-18(7-12-20(21)24)9-13-22(25)27-2/h5-7,9-13,16,24H,3-4,8,14-15H2,1-2H3/b13-9+
InChI Key ILICYNOMBXDZTR-UKTHLTGXSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H26O6
Molecular Weight 398.40 g/mol
Exact Mass 398.17293854 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.65
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Spiraformin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9927 99.27%
Caco-2 + 0.5432 54.32%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.9163 91.63%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.8659 86.59%
OATP1B3 inhibitior + 0.9300 93.00%
MATE1 inhibitior - 0.6400 64.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9721 97.21%
P-glycoprotein inhibitior + 0.7528 75.28%
P-glycoprotein substrate - 0.6182 61.82%
CYP3A4 substrate + 0.6194 61.94%
CYP2C9 substrate - 0.5936 59.36%
CYP2D6 substrate - 0.8632 86.32%
CYP3A4 inhibition + 0.5726 57.26%
CYP2C9 inhibition - 0.5735 57.35%
CYP2C19 inhibition + 0.6536 65.36%
CYP2D6 inhibition - 0.8233 82.33%
CYP1A2 inhibition + 0.6965 69.65%
CYP2C8 inhibition + 0.9130 91.30%
CYP inhibitory promiscuity - 0.7124 71.24%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8043 80.43%
Carcinogenicity (trinary) Non-required 0.7205 72.05%
Eye corrosion - 0.9942 99.42%
Eye irritation - 0.9434 94.34%
Skin irritation - 0.8734 87.34%
Skin corrosion - 0.9762 97.62%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8195 81.95%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation - 0.8978 89.78%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.7243 72.43%
Acute Oral Toxicity (c) III 0.6734 67.34%
Estrogen receptor binding + 0.8331 83.31%
Androgen receptor binding + 0.8404 84.04%
Thyroid receptor binding + 0.5747 57.47%
Glucocorticoid receptor binding + 0.6469 64.69%
Aromatase binding - 0.5119 51.19%
PPAR gamma + 0.6282 62.82%
Honey bee toxicity - 0.8834 88.34%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6800 68.00%
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 98.90% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 98.35% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.67% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.80% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.31% 96.00%
CHEMBL3194 P02766 Transthyretin 91.35% 90.71%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.69% 92.08%
CHEMBL2581 P07339 Cathepsin D 90.17% 98.95%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 89.20% 80.78%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.18% 95.56%
CHEMBL3437 Q16853 Amine oxidase, copper containing 88.94% 94.00%
CHEMBL221 P23219 Cyclooxygenase-1 88.13% 90.17%
CHEMBL4208 P20618 Proteasome component C5 87.76% 90.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.07% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.94% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.09% 94.45%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.74% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 82.66% 94.73%
CHEMBL2535 P11166 Glucose transporter 81.08% 98.75%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.34% 91.71%
CHEMBL1951 P21397 Monoamine oxidase A 80.03% 91.49%

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.
Spiraea formosana

Cross-Links

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PubChem 11350041
NPASS NPC77013
LOTUS LTS0236978
wikiData Q105115215