Doramectin congener 2

Details

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Internal ID 83005547-1da5-4336-8f83-1a997ba5bd2b
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (1S,2'R,3'S,10Z,12Z,14S,15S,16Z,19R,21S)-2'-cyclohexyl-7,15-dihydroxy-3',6,10,14,16-pentamethylspiro[2,20-dioxatricyclo[17.3.1.04,9]tricosa-4(9),5,7,10,12,16-hexaene-21,6'-2,3-dihydropyran]-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H48O6/c1-22-10-9-11-23(2)33(38)24(3)14-15-28-19-29(40-35(39)31-18-26(5)32(37)20-30(22)31)21-36(41-28)17-16-25(4)34(42-36)27-12-7-6-8-13-27/h9-11,14,16-18,20,23,25,27-29,33-34,37-38H,6-8,12-13,15,19,21H2,1-5H3/b11-9-,22-10-,24-14-/t23-,25-,28+,29-,33-,34-,36+/m0/s1
InChI Key JGHHZFRACXEISZ-WMUIGDBJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C36H48O6
Molecular Weight 576.80 g/mol
Exact Mass 576.34508925 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 7.60
Atomic LogP (AlogP) 7.58
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Doramectin congener 2

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9413 94.13%
Caco-2 - 0.7909 79.09%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8758 87.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8631 86.31%
OATP1B3 inhibitior + 0.9237 92.37%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9852 98.52%
P-glycoprotein inhibitior + 0.8468 84.68%
P-glycoprotein substrate + 0.6149 61.49%
CYP3A4 substrate + 0.6932 69.32%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8260 82.60%
CYP3A4 inhibition - 0.8118 81.18%
CYP2C9 inhibition - 0.7624 76.24%
CYP2C19 inhibition - 0.6226 62.26%
CYP2D6 inhibition - 0.9260 92.60%
CYP1A2 inhibition - 0.5681 56.81%
CYP2C8 inhibition + 0.6776 67.76%
CYP inhibitory promiscuity - 0.7170 71.70%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6027 60.27%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9402 94.02%
Skin irritation - 0.6578 65.78%
Skin corrosion - 0.9508 95.08%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7949 79.49%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.8010 80.10%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7438 74.38%
Acute Oral Toxicity (c) I 0.3065 30.65%
Estrogen receptor binding + 0.8892 88.92%
Androgen receptor binding + 0.7039 70.39%
Thyroid receptor binding + 0.5268 52.68%
Glucocorticoid receptor binding + 0.8681 86.81%
Aromatase binding + 0.6842 68.42%
PPAR gamma + 0.7457 74.57%
Honey bee toxicity - 0.7241 72.41%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9926 99.26%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.06% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.51% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.83% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.96% 97.09%
CHEMBL2581 P07339 Cathepsin D 90.76% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 90.44% 93.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.38% 99.23%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 89.64% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.62% 86.33%
CHEMBL218 P21554 Cannabinoid CB1 receptor 89.17% 96.61%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.10% 97.25%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.75% 93.40%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 87.92% 83.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.76% 96.09%
CHEMBL3012 Q13946 Phosphodiesterase 7A 86.19% 99.29%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 85.42% 95.58%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.37% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.57% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.49% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 84.25% 94.75%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.20% 91.07%
CHEMBL3401 O75469 Pregnane X receptor 84.17% 94.73%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 82.62% 97.33%
CHEMBL4530 P00488 Coagulation factor XIII 81.96% 96.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.93% 99.15%
CHEMBL230 P35354 Cyclooxygenase-2 81.72% 89.63%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.40% 90.71%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 80.53% 96.38%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.13% 93.04%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.13% 90.24%

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 139586108
LOTUS LTS0183622
wikiData Q77499010