16-Anhydrogitoxigenin

Details

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Internal ID afb5b1cd-f0f4-40c5-9c85-322474514c8d
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones
IUPAC Name 3-[(3S,5R,8R,9S,10S,13R,14S)-3,14-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15-dodecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H32O4/c1-21-8-5-16(24)12-15(21)3-4-19-18(21)6-9-22(2)17(7-10-23(19,22)26)14-11-20(25)27-13-14/h7,11,15-16,18-19,24,26H,3-6,8-10,12-13H2,1-2H3/t15-,16+,18+,19-,21+,22-,23+/m1/s1
InChI Key YGABECOLNBBTLH-OPBLIOOKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H32O4
Molecular Weight 372.50 g/mol
Exact Mass 372.23005950 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.52
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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RHODEXIN B
1FT289KX2B
NSC 160845
UNII-1FT289KX2B
Cardo-16,20(22)-dienolide, 3,14-dihydroxy-, (3beta,5beta)-
(3beta,5beta)-3,14-Dihydroxycardo-16,20(22)-dienolide
NSC-160845
SCHEMBL21578276
.DELTA.16-ANHYDROGITOXIGENIN
Q27896812
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 16-Anhydrogitoxigenin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.6816 68.16%
Blood Brain Barrier - 0.6645 66.45%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8605 86.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8934 89.34%
OATP1B3 inhibitior + 0.9667 96.67%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6493 64.93%
BSEP inhibitior + 0.9106 91.06%
P-glycoprotein inhibitior - 0.8628 86.28%
P-glycoprotein substrate + 0.6793 67.93%
CYP3A4 substrate + 0.7074 70.74%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9060 90.60%
CYP3A4 inhibition - 0.6717 67.17%
CYP2C9 inhibition - 0.9355 93.55%
CYP2C19 inhibition - 0.9237 92.37%
CYP2D6 inhibition - 0.9253 92.53%
CYP1A2 inhibition - 0.9045 90.45%
CYP2C8 inhibition - 0.7226 72.26%
CYP inhibitory promiscuity - 0.8681 86.81%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5341 53.41%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.9521 95.21%
Skin irritation - 0.5148 51.48%
Skin corrosion - 0.9425 94.25%
Ames mutagenesis - 0.6179 61.79%
Human Ether-a-go-go-Related Gene inhibition - 0.4864 48.64%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.6574 65.74%
skin sensitisation - 0.8671 86.71%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.5260 52.60%
Acute Oral Toxicity (c) III 0.4005 40.05%
Estrogen receptor binding + 0.8908 89.08%
Androgen receptor binding + 0.8322 83.22%
Thyroid receptor binding + 0.6716 67.16%
Glucocorticoid receptor binding + 0.9015 90.15%
Aromatase binding + 0.8255 82.55%
PPAR gamma - 0.5840 58.40%
Honey bee toxicity - 0.6866 68.66%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9922 99.22%

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
CHEMBL1994 P08235 Mineralocorticoid receptor 95.48% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.37% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.44% 97.25%
CHEMBL1871 P10275 Androgen Receptor 92.38% 96.43%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.48% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.18% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 89.06% 83.82%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.76% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.12% 95.56%
CHEMBL226 P30542 Adenosine A1 receptor 86.51% 95.93%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.87% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.26% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.76% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.80% 86.33%
CHEMBL2581 P07339 Cathepsin D 81.50% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 80.91% 94.75%

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.
Cryptostegia madagascariensis

Cross-Links

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PubChem 91809639
LOTUS LTS0001404
wikiData Q27896812