17-(2,6-Dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,8,10,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-7-one

Details

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Internal ID 00d62c96-a098-4cbe-a2c4-2e3a869f9cf9
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cucurbitacins
IUPAC Name 17-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,8,10,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-7-one
SMILES (Canonical) CC1(C(C(CC2C1=CC(=O)C3C2(CCC4(C3(CC(C4C(C)(C(=O)CCC(C)(C)O)O)O)C)C)C)O)O)C
SMILES (Isomeric) CC1(C(C(CC2C1=CC(=O)C3C2(CCC4(C3(CC(C4C(C)(C(=O)CCC(C)(C)O)O)O)C)C)C)O)O)C
InChI InChI=1S/C30H48O7/c1-25(2,36)10-9-21(34)30(8,37)23-20(33)15-29(7)22-18(31)13-16-17(14-19(32)24(35)26(16,3)4)27(22,5)11-12-28(23,29)6/h13,17,19-20,22-24,32-33,35-37H,9-12,14-15H2,1-8H3
InChI Key RVJJXMIGCLEWAG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48O7
Molecular Weight 520.70 g/mol
Exact Mass 520.34000387 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.94
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 17-(2,6-Dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,8,10,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-7-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9834 98.34%
Caco-2 - 0.6378 63.78%
Blood Brain Barrier + 0.8388 83.88%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8055 80.55%
OATP2B1 inhibitior - 0.8624 86.24%
OATP1B1 inhibitior + 0.7867 78.67%
OATP1B3 inhibitior + 0.8748 87.48%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7532 75.32%
BSEP inhibitior + 0.6378 63.78%
P-glycoprotein inhibitior - 0.5255 52.55%
P-glycoprotein substrate - 0.5343 53.43%
CYP3A4 substrate + 0.6771 67.71%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.8838 88.38%
CYP3A4 inhibition - 0.8060 80.60%
CYP2C9 inhibition - 0.8389 83.89%
CYP2C19 inhibition - 0.7834 78.34%
CYP2D6 inhibition - 0.9541 95.41%
CYP1A2 inhibition - 0.9254 92.54%
CYP2C8 inhibition - 0.6134 61.34%
CYP inhibitory promiscuity - 0.9150 91.50%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6943 69.43%
Eye corrosion - 0.9929 99.29%
Eye irritation - 0.9221 92.21%
Skin irritation + 0.6254 62.54%
Skin corrosion - 0.9371 93.71%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6591 65.91%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.5781 57.81%
skin sensitisation - 0.8018 80.18%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.8370 83.70%
Acute Oral Toxicity (c) I 0.5554 55.54%
Estrogen receptor binding + 0.7563 75.63%
Androgen receptor binding + 0.7659 76.59%
Thyroid receptor binding + 0.6364 63.64%
Glucocorticoid receptor binding + 0.7668 76.68%
Aromatase binding + 0.7374 73.74%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.7166 71.66%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9933 99.33%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.60% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.09% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.54% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.13% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.33% 94.45%
CHEMBL2581 P07339 Cathepsin D 91.29% 98.95%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 91.27% 94.78%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.78% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.89% 82.69%
CHEMBL226 P30542 Adenosine A1 receptor 85.66% 95.93%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.22% 89.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 82.61% 96.61%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.08% 86.33%
CHEMBL2179 P04062 Beta-glucocerebrosidase 82.06% 85.31%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.95% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.95% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.85% 96.77%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.21% 91.07%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.10% 96.90%

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.
Cayaponia racemosa

Cross-Links

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PubChem 162954837
LOTUS LTS0255353
wikiData Q105246075