2-[4-[2-[(1R,2E,4aR,4bS,8aS,10aS)-4b,8,8,10a-tetramethyl-2-(sulfooxymethylidene)-1,3,4,4a,5,6,7,8a,9,10-decahydrophenanthren-1-yl]ethyl]-5-oxo-2H-pyrrol-1-yl]acetic acid

Details

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Internal ID 52e0934e-15b4-4df0-8fb1-a1516c92f6c0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesterterpenoids > Cheilanthane sesterterpenoids
IUPAC Name 2-[4-[2-[(1R,2E,4aR,4bS,8aS,10aS)-4b,8,8,10a-tetramethyl-2-(sulfooxymethylidene)-1,3,4,4a,5,6,7,8a,9,10-decahydrophenanthren-1-yl]ethyl]-5-oxo-2H-pyrrol-1-yl]acetic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H41NO7S/c1-25(2)12-5-13-27(4)21(25)10-14-26(3)20(19(7-9-22(26)27)17-35-36(32,33)34)8-6-18-11-15-28(24(18)31)16-23(29)30/h11,17,20-22H,5-10,12-16H2,1-4H3,(H,29,30)(H,32,33,34)/b19-17+/t20-,21-,22-,26+,27-/m0/s1
InChI Key QCSNAPLPUTUYES-GYZFJBNPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H41NO7S
Molecular Weight 523.70 g/mol
Exact Mass 523.26037382 g/mol
Topological Polar Surface Area (TPSA) 130.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.98
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-[4-[2-[(1R,2E,4aR,4bS,8aS,10aS)-4b,8,8,10a-tetramethyl-2-(sulfooxymethylidene)-1,3,4,4a,5,6,7,8a,9,10-decahydrophenanthren-1-yl]ethyl]-5-oxo-2H-pyrrol-1-yl]acetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7366 73.66%
Caco-2 - 0.7531 75.31%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Plasma membrane 0.3899 38.99%
OATP2B1 inhibitior - 0.5683 56.83%
OATP1B1 inhibitior + 0.8439 84.39%
OATP1B3 inhibitior + 0.9291 92.91%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9682 96.82%
P-glycoprotein inhibitior + 0.6461 64.61%
P-glycoprotein substrate - 0.6634 66.34%
CYP3A4 substrate + 0.6921 69.21%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.9044 90.44%
CYP3A4 inhibition - 0.8424 84.24%
CYP2C9 inhibition - 0.7358 73.58%
CYP2C19 inhibition - 0.7029 70.29%
CYP2D6 inhibition - 0.8682 86.82%
CYP1A2 inhibition - 0.7494 74.94%
CYP2C8 inhibition + 0.5202 52.02%
CYP inhibitory promiscuity - 0.7828 78.28%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.5499 54.99%
Eye corrosion - 0.9787 97.87%
Eye irritation - 0.9287 92.87%
Skin irritation - 0.7591 75.91%
Skin corrosion - 0.9042 90.42%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5216 52.16%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.5976 59.76%
skin sensitisation - 0.8269 82.69%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.8242 82.42%
Acute Oral Toxicity (c) III 0.5966 59.66%
Estrogen receptor binding + 0.7883 78.83%
Androgen receptor binding + 0.6482 64.82%
Thyroid receptor binding + 0.5342 53.42%
Glucocorticoid receptor binding + 0.7904 79.04%
Aromatase binding + 0.7432 74.32%
PPAR gamma - 0.5103 51.03%
Honey bee toxicity - 0.8017 80.17%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9937 99.37%

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
CHEMBL2581 P07339 Cathepsin D 98.23% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.88% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.53% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 92.27% 82.69%
CHEMBL3524 P56524 Histone deacetylase 4 91.34% 92.97%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.58% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.81% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.47% 91.11%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.85% 94.33%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.71% 93.40%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.42% 97.25%
CHEMBL5028 O14672 ADAM10 85.65% 97.50%
CHEMBL5255 O00206 Toll-like receptor 4 85.19% 92.50%
CHEMBL284 P27487 Dipeptidyl peptidase IV 85.15% 95.69%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.23% 93.03%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.51% 95.50%
CHEMBL1902 P62942 FK506-binding protein 1A 82.40% 97.05%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.78% 100.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.65% 100.00%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.36% 99.18%

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.
There are no matching plants.

Cross-Links

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PubChem 42604185
LOTUS LTS0245900
wikiData Q105218549