2-amino-4-[7-hydroxy-2,4b,8,8,10a-pentamethyl-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-4,4a,5,6,7,8a,9,10-octahydro-1H-phenanthren-1-yl]butanoic acid

Details

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Internal ID 97b97da7-be8f-4207-b191-f505d561422f
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides
IUPAC Name 2-amino-4-[7-hydroxy-2,4b,8,8,10a-pentamethyl-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-4,4a,5,6,7,8a,9,10-octahydro-1H-phenanthren-1-yl]butanoic acid
SMILES (Canonical) CC1C(C(C(C(O1)OC2CC3(C(CCC4(C3CC=C(C4CCC(C(=O)O)N)C)C)C(C2O)(C)C)C)O)O)O
SMILES (Isomeric) CC1C(C(C(C(O1)OC2CC3(C(CCC4(C3CC=C(C4CCC(C(=O)O)N)C)C)C(C2O)(C)C)C)O)O)O
InChI InChI=1S/C29H49NO8/c1-14-7-10-20-28(5,16(14)8-9-17(30)25(35)36)12-11-19-27(3,4)24(34)18(13-29(19,20)6)38-26-23(33)22(32)21(31)15(2)37-26/h7,15-24,26,31-34H,8-13,30H2,1-6H3,(H,35,36)
InChI Key YJCRQRQABJDMCD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H49NO8
Molecular Weight 539.70 g/mol
Exact Mass 539.34581752 g/mol
Topological Polar Surface Area (TPSA) 163.00 Ų
XlogP -0.10
Atomic LogP (AlogP) 2.19
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-amino-4-[7-hydroxy-2,4b,8,8,10a-pentamethyl-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-4,4a,5,6,7,8a,9,10-octahydro-1H-phenanthren-1-yl]butanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8021 80.21%
Caco-2 - 0.8310 83.10%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.4232 42.32%
OATP2B1 inhibitior - 0.5801 58.01%
OATP1B1 inhibitior + 0.8875 88.75%
OATP1B3 inhibitior + 0.9028 90.28%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.5438 54.38%
P-glycoprotein substrate - 0.6657 66.57%
CYP3A4 substrate + 0.6860 68.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8491 84.91%
CYP3A4 inhibition - 0.8446 84.46%
CYP2C9 inhibition - 0.8447 84.47%
CYP2C19 inhibition - 0.7954 79.54%
CYP2D6 inhibition - 0.9122 91.22%
CYP1A2 inhibition - 0.8257 82.57%
CYP2C8 inhibition + 0.4589 45.89%
CYP inhibitory promiscuity - 0.8460 84.60%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6079 60.79%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9442 94.42%
Skin irritation - 0.6554 65.54%
Skin corrosion - 0.9182 91.82%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4691 46.91%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.8167 81.67%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.9380 93.80%
Acute Oral Toxicity (c) III 0.5966 59.66%
Estrogen receptor binding + 0.6003 60.03%
Androgen receptor binding + 0.5867 58.67%
Thyroid receptor binding + 0.5485 54.85%
Glucocorticoid receptor binding + 0.6113 61.13%
Aromatase binding + 0.6293 62.93%
PPAR gamma + 0.6481 64.81%
Honey bee toxicity - 0.8066 80.66%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5550 55.50%
Fish aquatic toxicity + 0.9025 90.25%

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
CHEMBL221 P23219 Cyclooxygenase-1 98.75% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.23% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.04% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.76% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.24% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.65% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.60% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.47% 93.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.63% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.78% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.49% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.18% 90.71%
CHEMBL3714130 P46095 G-protein coupled receptor 6 84.25% 97.36%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.96% 100.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.45% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.68% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.21% 94.45%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.54% 94.08%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.20% 97.25%
CHEMBL5028 O14672 ADAM10 80.11% 97.50%

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 162964114
LOTUS LTS0111941
wikiData Q105349183