(1S,4E,6R,10R,12E,14R,15S,17R,18S,19S,20S)-20-benzyl-6,15-dihydroxy-10,17,18-trimethyl-2,16-dioxa-21-azatetracyclo[12.8.0.01,19.015,17]docosa-4,12-diene-3,22-dione

Details

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Internal ID 32601a5f-d69b-4b46-b00f-7e180ec9e48e
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (1S,4E,6R,10R,12E,14R,15S,17R,18S,19S,20S)-20-benzyl-6,15-dihydroxy-10,17,18-trimethyl-2,16-dioxa-21-azatetracyclo[12.8.0.01,19.015,17]docosa-4,12-diene-3,22-dione
SMILES (Canonical) CC1CCCC(C=CC(=O)OC23C(C=CC1)C4(C(O4)(C(C2C(NC3=O)CC5=CC=CC=C5)C)C)O)O
SMILES (Isomeric) C[C@@H]1CCC[C@H](/C=C/C(=O)O[C@]23[C@@H](/C=C/C1)[C@]4([C@](O4)([C@H]([C@H]2[C@@H](NC3=O)CC5=CC=CC=C5)C)C)O)O
InChI InChI=1S/C29H37NO6/c1-18-9-7-13-21(31)15-16-24(32)35-28-23(14-8-10-18)29(34)27(3,36-29)19(2)25(28)22(30-26(28)33)17-20-11-5-4-6-12-20/h4-6,8,11-12,14-16,18-19,21-23,25,31,34H,7,9-10,13,17H2,1-3H3,(H,30,33)/b14-8+,16-15+/t18-,19+,21-,22+,23-,25+,27-,28-,29+/m1/s1
InChI Key XJJSRPWDIFDUMY-VWXSRXODSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H37NO6
Molecular Weight 495.60 g/mol
Exact Mass 495.26208790 g/mol
Topological Polar Surface Area (TPSA) 108.00 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.05
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,4E,6R,10R,12E,14R,15S,17R,18S,19S,20S)-20-benzyl-6,15-dihydroxy-10,17,18-trimethyl-2,16-dioxa-21-azatetracyclo[12.8.0.01,19.015,17]docosa-4,12-diene-3,22-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9505 95.05%
Caco-2 - 0.7908 79.08%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.5076 50.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8084 80.84%
OATP1B3 inhibitior + 0.9120 91.20%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7572 75.72%
BSEP inhibitior + 0.9123 91.23%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate + 0.6799 67.99%
CYP3A4 substrate + 0.6987 69.87%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8749 87.49%
CYP3A4 inhibition - 0.5182 51.82%
CYP2C9 inhibition - 0.8388 83.88%
CYP2C19 inhibition - 0.7887 78.87%
CYP2D6 inhibition - 0.9196 91.96%
CYP1A2 inhibition - 0.8761 87.61%
CYP2C8 inhibition + 0.6348 63.48%
CYP inhibitory promiscuity - 0.6942 69.42%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4507 45.07%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9630 96.30%
Skin irritation - 0.7242 72.42%
Skin corrosion - 0.9229 92.29%
Ames mutagenesis - 0.6370 63.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6975 69.75%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.5227 52.27%
skin sensitisation - 0.8396 83.96%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.5497 54.97%
Acute Oral Toxicity (c) III 0.3405 34.05%
Estrogen receptor binding + 0.7299 72.99%
Androgen receptor binding + 0.7005 70.05%
Thyroid receptor binding + 0.5375 53.75%
Glucocorticoid receptor binding + 0.7916 79.16%
Aromatase binding + 0.6935 69.35%
PPAR gamma + 0.7089 70.89%
Honey bee toxicity - 0.7770 77.70%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9652 96.52%

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 99.18% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.03% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.97% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.76% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.41% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.30% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.00% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.33% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.39% 95.50%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 85.86% 97.64%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.02% 93.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.98% 99.23%
CHEMBL221 P23219 Cyclooxygenase-1 83.93% 90.17%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.90% 96.25%
CHEMBL4523377 Q86WV6 Stimulator of interferon genes protein 83.55% 95.48%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.24% 97.25%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 81.07% 95.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.42% 94.45%

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 163187067
LOTUS LTS0016572
wikiData Q105329010