4,6,8,10,12,14,15,16,27-Nonahydroxy-3-(1-hydroxybutyl)-17,28-dimethyl-1-oxacyclooctacosa-17,19,21,23,25-pentaen-2-one

Details

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Internal ID 9400f803-a1b3-4529-9064-109f32417b3f
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 4,6,8,10,12,14,15,16,27-nonahydroxy-3-(1-hydroxybutyl)-17,28-dimethyl-1-oxacyclooctacosa-17,19,21,23,25-pentaen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C33H54O12/c1-4-12-27(39)30-28(40)18-24(36)16-22(34)15-23(35)17-25(37)19-29(41)32(43)31(42)20(2)13-10-8-6-5-7-9-11-14-26(38)21(3)45-33(30)44/h5-11,13-14,21-32,34-43H,4,12,15-19H2,1-3H3
InChI Key MELIVMKAQSVXIP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C33H54O12
Molecular Weight 642.80 g/mol
Exact Mass 642.36152715 g/mol
Topological Polar Surface Area (TPSA) 229.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.08
H-Bond Acceptor 12
H-Bond Donor 10
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,6,8,10,12,14,15,16,27-Nonahydroxy-3-(1-hydroxybutyl)-17,28-dimethyl-1-oxacyclooctacosa-17,19,21,23,25-pentaen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7360 73.60%
Caco-2 - 0.8736 87.36%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6277 62.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9268 92.68%
OATP1B3 inhibitior + 0.9471 94.71%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.6009 60.09%
P-glycoprotein inhibitior - 0.7585 75.85%
P-glycoprotein substrate + 0.5832 58.32%
CYP3A4 substrate + 0.6151 61.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8786 87.86%
CYP3A4 inhibition - 0.7080 70.80%
CYP2C9 inhibition - 0.8956 89.56%
CYP2C19 inhibition + 0.5069 50.69%
CYP2D6 inhibition - 0.9214 92.14%
CYP1A2 inhibition - 0.9171 91.71%
CYP2C8 inhibition - 0.8309 83.09%
CYP inhibitory promiscuity - 0.9487 94.87%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6641 66.41%
Eye corrosion - 0.9814 98.14%
Eye irritation - 0.9388 93.88%
Skin irritation - 0.6429 64.29%
Skin corrosion - 0.9190 91.90%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8147 81.47%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.5768 57.68%
skin sensitisation - 0.7848 78.48%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.5783 57.83%
Acute Oral Toxicity (c) III 0.4892 48.92%
Estrogen receptor binding + 0.7771 77.71%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5252 52.52%
Glucocorticoid receptor binding + 0.5372 53.72%
Aromatase binding - 0.5300 53.00%
PPAR gamma + 0.5752 57.52%
Honey bee toxicity - 0.7712 77.12%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.8022 80.22%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.91% 97.25%
CHEMBL2581 P07339 Cathepsin D 94.97% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.44% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.07% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.83% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.66% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.63% 99.23%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.69% 93.56%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.07% 97.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.54% 89.00%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 81.55% 95.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.53% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.24% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.72% 96.95%

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 163056278
LOTUS LTS0033545
wikiData Q104171611