Dacryhainansterone

Details

Top
Internal ID 9a32725d-37a9-41bb-8ca7-bbcc795dedb9
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Bile acids, alcohols and derivatives > Hydroxy bile acids, alcohols and derivatives > Pentahydroxy bile acids, alcohols and derivatives
IUPAC Name (2S,3R,5R,10S,13R,14S,17S)-17-[(2R,3R)-2,3-dihydroxy-6-methylheptan-2-yl]-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H42O6/c1-15(2)6-7-23(31)26(5,32)22-9-11-27(33)17-12-19(28)18-13-20(29)21(30)14-24(18,3)16(17)8-10-25(22,27)4/h8,12,15,18,20-23,29-33H,6-7,9-11,13-14H2,1-5H3/t18-,20+,21-,22-,23+,24+,25+,26+,27+/m0/s1
InChI Key HHSAPBUKXSETPT-ZTUUSGHWSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C27H42O6
Molecular Weight 462.60 g/mol
Exact Mass 462.29813906 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 6
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

Top
CHEMBL2086401

2D Structure

Top
2D Structure of Dacryhainansterone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.5597 55.97%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8310 83.10%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.9116 91.16%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.6426 64.26%
P-glycoprotein inhibitior - 0.6855 68.55%
P-glycoprotein substrate + 0.6264 62.64%
CYP3A4 substrate + 0.7118 71.18%
CYP2C9 substrate - 0.8117 81.17%
CYP2D6 substrate - 0.8668 86.68%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.8690 86.90%
CYP2C19 inhibition - 0.8364 83.64%
CYP2D6 inhibition - 0.9516 95.16%
CYP1A2 inhibition - 0.9278 92.78%
CYP2C8 inhibition - 0.6046 60.46%
CYP inhibitory promiscuity - 0.8761 87.61%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6900 69.00%
Eye corrosion - 0.9944 99.44%
Eye irritation - 0.9463 94.63%
Skin irritation + 0.6543 65.43%
Skin corrosion - 0.9489 94.89%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4574 45.74%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.5417 54.17%
skin sensitisation - 0.7034 70.34%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.8289 82.89%
Acute Oral Toxicity (c) III 0.5365 53.65%
Estrogen receptor binding + 0.7942 79.42%
Androgen receptor binding + 0.7211 72.11%
Thyroid receptor binding + 0.6299 62.99%
Glucocorticoid receptor binding + 0.7670 76.70%
Aromatase binding + 0.6608 66.08%
PPAR gamma - 0.5426 54.26%
Honey bee toxicity - 0.7776 77.76%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9934 99.34%

Targets

Top

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 99.81% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.55% 85.14%
CHEMBL2581 P07339 Cathepsin D 97.50% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.21% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.59% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 94.43% 96.61%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.77% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 92.14% 97.79%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.38% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.06% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.44% 82.69%
CHEMBL4040 P28482 MAP kinase ERK2 89.92% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.73% 95.56%
CHEMBL2179 P04062 Beta-glucocerebrosidase 88.45% 85.31%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.24% 97.14%
CHEMBL4227 P25090 Lipoxin A4 receptor 87.64% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.54% 95.89%
CHEMBL226 P30542 Adenosine A1 receptor 86.75% 95.93%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 86.61% 94.78%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.34% 91.07%
CHEMBL2094135 Q96BI3 Gamma-secretase 84.42% 98.05%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.00% 93.56%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 83.19% 90.24%
CHEMBL332 P03956 Matrix metalloproteinase-1 83.11% 94.50%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.93% 93.99%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 82.68% 96.90%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.37% 100.00%
CHEMBL1871 P10275 Androgen Receptor 81.80% 96.43%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 81.13% 94.23%
CHEMBL1937 Q92769 Histone deacetylase 2 80.84% 94.75%

Plants that contains it

Top
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.
Rhaponticum carthamoides subsp. carthamoides
Serratula coronata

Cross-Links

Top
PubChem 13829647
LOTUS LTS0165611
wikiData Q105028532