Catalposide

Details

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Internal ID 9d41b209-3da8-4920-adab-8e88ecef79d6
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name [(1S,2S,4S,5S,6R,10S)-2-(hydroxymethyl)-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-5-yl] 4-hydroxybenzoate
SMILES (Canonical) C1=COC(C2C1C(C3C2(O3)CO)OC(=O)C4=CC=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O
SMILES (Isomeric) C1=CO[C@H]([C@H]2[C@@H]1[C@@H]([C@H]3[C@@]2(O3)CO)OC(=O)C4=CC=C(C=C4)O)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O
InChI InChI=1S/C22H26O12/c23-7-12-14(26)15(27)16(28)21(31-12)33-20-13-11(5-6-30-20)17(18-22(13,8-24)34-18)32-19(29)9-1-3-10(25)4-2-9/h1-6,11-18,20-21,23-28H,7-8H2/t11-,12-,13-,14-,15+,16-,17+,18+,20+,21+,22-/m1/s1
InChI Key UXSACQOOWZMGSE-RWORTQBESA-N
Popularity 29 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O12
Molecular Weight 482.40 g/mol
Exact Mass 482.14242626 g/mol
Topological Polar Surface Area (TPSA) 188.00 Ų
XlogP -1.30
Atomic LogP (AlogP) -2.02
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 6

Synonyms

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6736-85-2
Hydroxybenzoyl catalpol
EINECS 229-789-1
UNII-7KD7K3964H
CHEMBL2332354
7KD7K3964H
1a(S)alpha,1bbeta,2beta,5abeta,6beta,6aalpha-Hexahydro-6-((4-hydroxybenzoyl)oxy)-1a-(hydroxymethyl)oxireno(4,5)cyclopenta(1,2-c)pyran-2-yl beta-D-glucopyranoside
beta-D-Glucopyranoside, 1a,1b,2,5a,6,6a-hexahydro-6-((4-hydroxybenzoyl)oxy)-1a-(hydroxymethyl)oxireno(4,5)cyclopenta(1,2-c)pyran-2-yl, (1aS-(1a-alpha,1b-beta,2-beta,5a-beta,6-beta,6a-alpha))-
C22H26O12
C22-H26-O12
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Catalposide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5631 56.31%
Caco-2 - 0.9138 91.38%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.6002 60.02%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.7629 76.29%
OATP1B3 inhibitior + 0.9565 95.65%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7090 70.90%
P-glycoprotein inhibitior - 0.6577 65.77%
P-glycoprotein substrate - 0.6988 69.88%
CYP3A4 substrate + 0.6593 65.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8522 85.22%
CYP3A4 inhibition - 0.9111 91.11%
CYP2C9 inhibition - 0.8998 89.98%
CYP2C19 inhibition - 0.7733 77.33%
CYP2D6 inhibition - 0.8787 87.87%
CYP1A2 inhibition - 0.8773 87.73%
CYP2C8 inhibition + 0.6769 67.69%
CYP inhibitory promiscuity - 0.7594 75.94%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5420 54.20%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.9403 94.03%
Skin irritation - 0.7661 76.61%
Skin corrosion - 0.9476 94.76%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5990 59.90%
Micronuclear - 0.5267 52.67%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.7853 78.53%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5627 56.27%
Acute Oral Toxicity (c) III 0.4388 43.88%
Estrogen receptor binding + 0.7092 70.92%
Androgen receptor binding + 0.5211 52.11%
Thyroid receptor binding + 0.6121 61.21%
Glucocorticoid receptor binding - 0.4915 49.15%
Aromatase binding + 0.6774 67.74%
PPAR gamma + 0.7339 73.39%
Honey bee toxicity - 0.7751 77.51%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6750 67.50%
Fish aquatic toxicity + 0.7544 75.44%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 12 nM
Kd
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.26% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 91.54% 91.49%
CHEMBL211 P08172 Muscarinic acetylcholine receptor M2 91.36% 94.97%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.28% 86.33%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 88.30% 94.23%
CHEMBL2581 P07339 Cathepsin D 88.22% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.98% 94.00%
CHEMBL4208 P20618 Proteasome component C5 87.96% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.61% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.43% 99.17%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 86.22% 89.67%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.05% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.59% 89.00%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 84.17% 83.57%
CHEMBL3232685 O00257 E3 SUMO-protein ligase CBX4 84.00% 93.00%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 83.86% 95.83%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.17% 95.56%
CHEMBL3194 P02766 Transthyretin 82.92% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.38% 95.89%
CHEMBL5255 O00206 Toll-like receptor 4 80.33% 92.50%

Plants that contains it

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Cross-Links

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PubChem 93039
NPASS NPC194705
LOTUS LTS0109915
wikiData Q76009675