2,9,10,11-Tetrahydroxy-4,6,12,17,17-pentamethyl-18-(3,4,5-trihydroxyoxan-2-yl)oxyhexacyclo[11.9.0.01,21.04,12.05,10.016,21]docos-13-en-8-one

Details

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Internal ID b193a029-874e-4b90-a6f8-55aa00a4e587
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides
IUPAC Name 2,9,10,11-tetrahydroxy-4,6,12,17,17-pentamethyl-18-(3,4,5-trihydroxyoxan-2-yl)oxyhexacyclo[11.9.0.01,21.04,12.05,10.016,21]docos-13-en-8-one
SMILES (Canonical) CC1CC(=O)C(C2(C1C3(CC(C45CC46CCC(C(C6CC=C5C3(C2O)C)(C)C)OC7C(C(C(CO7)O)O)O)O)C)O)O
SMILES (Isomeric) CC1CC(=O)C(C2(C1C3(CC(C45CC46CCC(C(C6CC=C5C3(C2O)C)(C)C)OC7C(C(C(CO7)O)O)O)O)C)O)O
InChI InChI=1S/C32H48O10/c1-14-10-15(33)24(38)32(40)23(14)28(4)11-19(35)31-13-30(31)9-8-20(42-25-22(37)21(36)16(34)12-41-25)27(2,3)17(30)6-7-18(31)29(28,5)26(32)39/h7,14,16-17,19-26,34-40H,6,8-13H2,1-5H3
InChI Key ZJUGPUXCDPEPDX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H48O10
Molecular Weight 592.70 g/mol
Exact Mass 592.32474772 g/mol
Topological Polar Surface Area (TPSA) 177.00 Ų
XlogP -0.20
Atomic LogP (AlogP) 0.42
H-Bond Acceptor 10
H-Bond Donor 7
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,9,10,11-Tetrahydroxy-4,6,12,17,17-pentamethyl-18-(3,4,5-trihydroxyoxan-2-yl)oxyhexacyclo[11.9.0.01,21.04,12.05,10.016,21]docos-13-en-8-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9321 93.21%
Caco-2 - 0.8167 81.67%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8144 81.44%
OATP2B1 inhibitior - 0.5879 58.79%
OATP1B1 inhibitior + 0.8301 83.01%
OATP1B3 inhibitior + 0.9027 90.27%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7318 73.18%
BSEP inhibitior - 0.5971 59.71%
P-glycoprotein inhibitior + 0.6091 60.91%
P-glycoprotein substrate + 0.5864 58.64%
CYP3A4 substrate + 0.7344 73.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8595 85.95%
CYP3A4 inhibition - 0.9124 91.24%
CYP2C9 inhibition - 0.6515 65.15%
CYP2C19 inhibition - 0.8411 84.11%
CYP2D6 inhibition - 0.9213 92.13%
CYP1A2 inhibition - 0.7552 75.52%
CYP2C8 inhibition + 0.6475 64.75%
CYP inhibitory promiscuity - 0.9310 93.10%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6629 66.29%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.9288 92.88%
Skin irritation - 0.5495 54.95%
Skin corrosion - 0.9357 93.57%
Ames mutagenesis - 0.6140 61.40%
Human Ether-a-go-go-Related Gene inhibition + 0.7494 74.94%
Micronuclear - 0.7200 72.00%
Hepatotoxicity - 0.6413 64.13%
skin sensitisation - 0.8530 85.30%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.8452 84.52%
Acute Oral Toxicity (c) III 0.4822 48.22%
Estrogen receptor binding + 0.5960 59.60%
Androgen receptor binding + 0.7780 77.80%
Thyroid receptor binding - 0.5202 52.02%
Glucocorticoid receptor binding + 0.6092 60.92%
Aromatase binding + 0.6658 66.58%
PPAR gamma + 0.5656 56.56%
Honey bee toxicity - 0.7284 72.84%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5750 57.50%
Fish aquatic toxicity + 0.9813 98.13%

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 95.64% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.41% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.87% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.76% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.90% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.51% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.43% 89.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 89.70% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.62% 97.09%
CHEMBL1871 P10275 Androgen Receptor 85.35% 96.43%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.25% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.76% 92.94%
CHEMBL4208 P20618 Proteasome component C5 84.17% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.12% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.56% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.36% 91.07%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.05% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.88% 97.14%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.83% 86.00%

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.
Actaea cimicifuga
Actaea yunnanensis

Cross-Links

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PubChem 85090814
LOTUS LTS0241302
wikiData Q105378166