Cinnacasolide C

Details

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Internal ID 60d708c2-ca30-4a1f-b526-664c5a1c6081
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[3-methoxy-4-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]phenoxy]oxane-3,4,5-triol
SMILES (Canonical) COC1=C(C=CC(=C1)OC2=C(C=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC)OC4C(C(C(C(O4)CO)O)O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)OC2=C(C=C(C=C2)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)OC)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
InChI InChI=1S/C26H34O15/c1-35-15-8-12(38-25-23(33)21(31)19(29)17(9-27)40-25)4-5-13(15)37-11-3-6-14(16(7-11)36-2)39-26-24(34)22(32)20(30)18(10-28)41-26/h3-8,17-34H,9-10H2,1-2H3/t17-,18-,19-,20-,21+,22+,23-,24-,25-,26-/m1/s1
InChI Key BRGMLXAIQVVQOP-PCIRLDFKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H34O15
Molecular Weight 586.50 g/mol
Exact Mass 586.18977037 g/mol
Topological Polar Surface Area (TPSA) 226.00 Ų
XlogP -0.90
Atomic LogP (AlogP) -2.15
H-Bond Acceptor 15
H-Bond Donor 8
Rotatable Bonds 10

Synonyms

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CHEMBL2048806
BDBM50485313

2D Structure

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2D Structure of Cinnacasolide C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8824 88.24%
Caco-2 - 0.8593 85.93%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6032 60.32%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.9130 91.30%
OATP1B3 inhibitior + 0.9683 96.83%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8410 84.10%
P-glycoprotein inhibitior - 0.4585 45.85%
P-glycoprotein substrate - 0.9177 91.77%
CYP3A4 substrate + 0.5164 51.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8010 80.10%
CYP3A4 inhibition - 0.9330 93.30%
CYP2C9 inhibition - 0.9054 90.54%
CYP2C19 inhibition - 0.8874 88.74%
CYP2D6 inhibition - 0.9215 92.15%
CYP1A2 inhibition - 0.9266 92.66%
CYP2C8 inhibition + 0.4434 44.34%
CYP inhibitory promiscuity - 0.7558 75.58%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6766 67.66%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9238 92.38%
Skin irritation - 0.8679 86.79%
Skin corrosion - 0.9626 96.26%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7849 78.49%
Micronuclear - 0.5041 50.41%
Hepatotoxicity - 0.8467 84.67%
skin sensitisation - 0.8944 89.44%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.6324 63.24%
Acute Oral Toxicity (c) III 0.7588 75.88%
Estrogen receptor binding + 0.7375 73.75%
Androgen receptor binding - 0.5262 52.62%
Thyroid receptor binding + 0.5698 56.98%
Glucocorticoid receptor binding - 0.5269 52.69%
Aromatase binding + 0.5792 57.92%
PPAR gamma + 0.6542 65.42%
Honey bee toxicity - 0.8876 88.76%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6549 65.49%
Fish aquatic toxicity - 0.4706 47.06%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.27% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.61% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.41% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.06% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.55% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.63% 86.33%
CHEMBL4208 P20618 Proteasome component C5 89.10% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.69% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.30% 92.94%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.85% 86.92%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.19% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.44% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 81.96% 94.73%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.44% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.45% 92.62%

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.
Neolitsea cassia

Cross-Links

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PubChem 70694646
NPASS NPC247146