[(1S,2S,4aR,4bS,6aS,11aS,11bR,13aR)-2,10-dihydroxy-1,4a,6a,11b-tetramethyl-1-[2-[(1S)-2,6,6-trimethylcyclohex-2-en-1-yl]ethyl]-3,4,4b,5,6,11,11a,12,13,13a-decahydro-2H-indeno[2,1-a]phenanthren-7-yl] hydrogen sulfate

Details

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Internal ID 42304f4f-4d74-4eae-a3d3-44aee9958398
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives
IUPAC Name [(1S,2S,4aR,4bS,6aS,11aS,11bR,13aR)-2,10-dihydroxy-1,4a,6a,11b-tetramethyl-1-[2-[(1S)-2,6,6-trimethylcyclohex-2-en-1-yl]ethyl]-3,4,4b,5,6,11,11a,12,13,13a-decahydro-2H-indeno[2,1-a]phenanthren-7-yl] hydrogen sulfate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H54O6S/c1-22-9-8-16-32(2,3)24(22)12-17-35(6)28-13-18-34(5)27(33(28,4)20-15-30(35)38)14-19-36(7)29(34)21-23-25(37)10-11-26(31(23)36)42-43(39,40)41/h9-11,24,27-30,37-38H,8,12-21H2,1-7H3,(H,39,40,41)/t24-,27-,28-,29+,30+,33-,34-,35+,36+/m1/s1
InChI Key BWFQGFRYCUEONM-YUSBHCCRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C36H54O6S
Molecular Weight 614.90 g/mol
Exact Mass 614.36411061 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 9.10
Atomic LogP (AlogP) 8.16
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2S,4aR,4bS,6aS,11aS,11bR,13aR)-2,10-dihydroxy-1,4a,6a,11b-tetramethyl-1-[2-[(1S)-2,6,6-trimethylcyclohex-2-en-1-yl]ethyl]-3,4,4b,5,6,11,11a,12,13,13a-decahydro-2H-indeno[2,1-a]phenanthren-7-yl] hydrogen sulfate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9881 98.81%
Caco-2 - 0.7769 77.69%
Blood Brain Barrier + 0.6638 66.38%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5316 53.16%
OATP2B1 inhibitior - 0.5648 56.48%
OATP1B1 inhibitior + 0.9078 90.78%
OATP1B3 inhibitior + 0.9270 92.70%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9718 97.18%
P-glycoprotein inhibitior + 0.7602 76.02%
P-glycoprotein substrate + 0.5822 58.22%
CYP3A4 substrate + 0.7220 72.20%
CYP2C9 substrate - 0.7724 77.24%
CYP2D6 substrate - 0.7168 71.68%
CYP3A4 inhibition - 0.7741 77.41%
CYP2C9 inhibition - 0.7766 77.66%
CYP2C19 inhibition - 0.7117 71.17%
CYP2D6 inhibition - 0.8683 86.83%
CYP1A2 inhibition - 0.7452 74.52%
CYP2C8 inhibition + 0.7721 77.21%
CYP inhibitory promiscuity + 0.5879 58.79%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.6318 63.18%
Eye corrosion - 0.9854 98.54%
Eye irritation - 0.9236 92.36%
Skin irritation - 0.7382 73.82%
Skin corrosion - 0.8438 84.38%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6530 65.30%
Micronuclear + 0.5400 54.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation - 0.7905 79.05%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 1.0000 100.00%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.7130 71.30%
Acute Oral Toxicity (c) III 0.5982 59.82%
Estrogen receptor binding + 0.6869 68.69%
Androgen receptor binding + 0.6705 67.05%
Thyroid receptor binding + 0.5665 56.65%
Glucocorticoid receptor binding + 0.7626 76.26%
Aromatase binding + 0.7450 74.50%
PPAR gamma + 0.6440 64.40%
Honey bee toxicity - 0.7780 77.80%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5750 57.50%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.41% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.15% 97.09%
CHEMBL220 P22303 Acetylcholinesterase 94.25% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.75% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.39% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.55% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.37% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.90% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.71% 92.94%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 86.12% 89.05%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.05% 97.21%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.17% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.16% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 81.43% 94.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.43% 99.15%
CHEMBL2179 P04062 Beta-glucocerebrosidase 81.26% 85.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.39% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.18% 94.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10508318
LOTUS LTS0175014
wikiData Q104947211