Reoselin A

Details

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Internal ID 89a100fb-4952-41f1-aaa0-6315c0694e04
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name 7-[(2E,6E,10S)-10-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-11-hydroxy-3,7,11-trimethyldodeca-2,6-dienoxy]chromen-2-one
SMILES (Canonical) CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)CCC(C(C)(C)O)OC3C(C(C(C(O3)CO)O)O)OC4C(C(C(C(O4)CO)O)O)O
SMILES (Isomeric) C/C(=C\CC/C(=C/COC1=CC2=C(C=C1)C=CC(=O)O2)/C)/CC[C@@H](C(C)(C)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
InChI InChI=1S/C36H52O15/c1-19(6-5-7-20(2)14-15-46-22-11-9-21-10-13-27(39)47-23(21)16-22)8-12-26(36(3,4)45)50-35-33(31(43)29(41)25(18-38)49-35)51-34-32(44)30(42)28(40)24(17-37)48-34/h6,9-11,13-14,16,24-26,28-35,37-38,40-45H,5,7-8,12,15,17-18H2,1-4H3/b19-6+,20-14+/t24-,25-,26+,28-,29-,30+,31+,32-,33-,34+,35+/m1/s1
InChI Key IRJOYYJBFNUUNS-HYEWAJBBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C36H52O15
Molecular Weight 724.80 g/mol
Exact Mass 724.33062095 g/mol
Topological Polar Surface Area (TPSA) 234.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 0.41
H-Bond Acceptor 15
H-Bond Donor 8
Rotatable Bonds 16

Synonyms

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Reoselin
Rheozelin A
BRN 1675994
53011-70-4
2H-1-Benzopyran-2-one, 7-((10-((2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy)-11-hydroxy-3,7,11-trimethyl-2,6-dodecadienyl)oxy)-, (S-(E,E))-

2D Structure

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2D Structure of Reoselin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7718 77.18%
Caco-2 - 0.8667 86.67%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8381 83.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8512 85.12%
OATP1B3 inhibitior - 0.3260 32.60%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7026 70.26%
BSEP inhibitior + 0.9195 91.95%
P-glycoprotein inhibitior + 0.7462 74.62%
P-glycoprotein substrate - 0.5252 52.52%
CYP3A4 substrate + 0.6869 68.69%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8539 85.39%
CYP3A4 inhibition - 0.9180 91.80%
CYP2C9 inhibition - 0.7973 79.73%
CYP2C19 inhibition - 0.7401 74.01%
CYP2D6 inhibition - 0.9165 91.65%
CYP1A2 inhibition - 0.6873 68.73%
CYP2C8 inhibition + 0.5062 50.62%
CYP inhibitory promiscuity - 0.8815 88.15%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6556 65.56%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9160 91.60%
Skin irritation - 0.7350 73.50%
Skin corrosion - 0.9519 95.19%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7594 75.94%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.7177 71.77%
skin sensitisation - 0.8893 88.93%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.7432 74.32%
Acute Oral Toxicity (c) III 0.6191 61.91%
Estrogen receptor binding + 0.7659 76.59%
Androgen receptor binding + 0.7309 73.09%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7167 71.67%
Aromatase binding + 0.6591 65.91%
PPAR gamma + 0.7512 75.12%
Honey bee toxicity - 0.6830 68.30%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9934 99.34%

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 99.29% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 98.23% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.28% 99.17%
CHEMBL2039 P27338 Monoamine oxidase B 96.95% 92.51%
CHEMBL2581 P07339 Cathepsin D 96.55% 98.95%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 94.26% 83.57%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.66% 94.00%
CHEMBL220 P22303 Acetylcholinesterase 90.33% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 90.13% 91.49%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.65% 92.08%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.75% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.60% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.53% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.28% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.59% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.26% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 82.55% 93.31%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.55% 100.00%
CHEMBL4581 P52732 Kinesin-like protein 1 82.21% 93.18%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.00% 97.36%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.47% 90.71%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.30% 97.25%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.03% 93.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.21% 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.
Ferula kirialovii
Ferula korshinskyi
Ferula moschata

Cross-Links

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PubChem 6445962
LOTUS LTS0254352
wikiData Q76387481