CID 3086140

Details

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Internal ID 7a4c17c6-a7ec-4c50-b413-546b131a3dde
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name (1S,22S,23S,25R,26R,28S,31S,33S)-22-hydroxy-1,10,10,12,12,30,30,36-octamethyl-28-(2-methylprop-1-enyl)-11,24,27,29,32-pentaoxa-3-azadecacyclo[17.17.0.02,17.04,16.07,15.09,13.022,36.023,25.023,33.026,31]hexatriaconta-2(17),4(16),5,7(15)-tetraen-8-one
SMILES (Canonical) CC(=CC1OC2C(C(O1)(C)C)OC3CCC4(C5(C(CCC4(C36C2O6)O)CC7=C5NC8=C7C9=C(C=C8)C(=O)C1C(C9)C(OC1(C)C)(C)C)C)C)C
SMILES (Isomeric) CC(=C[C@H]1O[C@H]2[C@@H]3[C@@]4(O3)[C@H](CCC5([C@]4(CCC6[C@@]5(C7=C(C6)C8=C(N7)C=CC9=C8CC3C(C9=O)C(OC3(C)C)(C)C)C)O)C)O[C@@H]2C(O1)(C)C)C
InChI InChI=1S/C42H55NO7/c1-20(2)17-28-47-32-34(38(7,8)48-28)46-27-14-15-39(9)40(10)21(13-16-41(39,45)42(27)35(32)49-42)18-24-29-23-19-25-30(37(5,6)50-36(25,3)4)31(44)22(23)11-12-26(29)43-33(24)40/h11-12,17,21,25,27-28,30,32,34-35,43,45H,13-16,18-19H2,1-10H3/t21?,25?,27-,28-,30?,32+,34-,35+,39?,40+,41-,42-/m0/s1
InChI Key HGBZMCXKHKZYBF-LIHFUKCQSA-N
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C42H55NO7
Molecular Weight 685.90 g/mol
Exact Mass 685.39785309 g/mol
Topological Polar Surface Area (TPSA) 103.00 Ų
XlogP 5.80
Atomic LogP (AlogP) 6.87
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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(1S,22S,23S,25R,26R,28S,31S,33S)-22-Hydroxy-1,10,10,12,12,30,30,36-octamethyl-28-(2-methylprop-1-enyl)-11,24,27,29,32-pentaoxa-3-azadecacyclo[17.17.0.02,17.04,16.07,15.09,13.022,36.023,25.023,33.026,31]hexatriaconta-2(17),4(16),5,7(15)-tetraen-8-one

2D Structure

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2D Structure of CID 3086140

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9840 98.40%
Caco-2 - 0.8201 82.01%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.3981 39.81%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.8265 82.65%
OATP1B3 inhibitior + 0.9181 91.81%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8321 83.21%
BSEP inhibitior + 0.9873 98.73%
P-glycoprotein inhibitior + 0.7923 79.23%
P-glycoprotein substrate + 0.7281 72.81%
CYP3A4 substrate + 0.7396 73.96%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8606 86.06%
CYP3A4 inhibition - 0.7347 73.47%
CYP2C9 inhibition - 0.8227 82.27%
CYP2C19 inhibition - 0.8117 81.17%
CYP2D6 inhibition - 0.9138 91.38%
CYP1A2 inhibition + 0.6940 69.40%
CYP2C8 inhibition + 0.7040 70.40%
CYP inhibitory promiscuity - 0.7827 78.27%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5138 51.38%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9156 91.56%
Skin irritation - 0.7048 70.48%
Skin corrosion - 0.9241 92.41%
Ames mutagenesis + 0.5266 52.66%
Human Ether-a-go-go-Related Gene inhibition + 0.6530 65.30%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.7960 79.60%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.8574 85.74%
Acute Oral Toxicity (c) III 0.5201 52.01%
Estrogen receptor binding + 0.7787 77.87%
Androgen receptor binding + 0.7669 76.69%
Thyroid receptor binding + 0.5853 58.53%
Glucocorticoid receptor binding + 0.8085 80.85%
Aromatase binding + 0.7374 73.74%
PPAR gamma + 0.7406 74.06%
Honey bee toxicity - 0.7252 72.52%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9875 98.75%

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
CHEMBL1951 P21397 Monoamine oxidase A 97.38% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.79% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.93% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.88% 89.00%
CHEMBL2581 P07339 Cathepsin D 95.16% 98.95%
CHEMBL1902 P62942 FK506-binding protein 1A 94.68% 97.05%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.99% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 92.11% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.75% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 91.57% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.18% 95.89%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.01% 93.40%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.74% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.50% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.67% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.66% 99.23%
CHEMBL3922 P50579 Methionine aminopeptidase 2 85.10% 97.28%
CHEMBL3310 Q96DB2 Histone deacetylase 11 83.20% 88.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.82% 89.34%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.27% 97.09%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.43% 91.71%

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.
Lolium perenne

Cross-Links

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PubChem 3086140
LOTUS LTS0248930
wikiData Q28036875