(3R,4R,6R,10S,12S,14S,16S,17E,19E,21E,23E,25E,27S,28S)-4,6,10,12,14,16-hexahydroxy-3,27,28-trimethyl-1-oxacyclooctacosa-17,19,21,23,25-pentaen-2-one

Details

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Internal ID 129061f9-c1af-478e-9cd5-4251f1725b11
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (3R,4R,6R,10S,12S,14S,16S,17E,19E,21E,23E,25E,27S,28S)-4,6,10,12,14,16-hexahydroxy-3,27,28-trimethyl-1-oxacyclooctacosa-17,19,21,23,25-pentaen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H48O8/c1-21-13-10-8-6-4-5-7-9-11-14-24(31)17-27(34)19-28(35)18-25(32)15-12-16-26(33)20-29(36)22(2)30(37)38-23(21)3/h4-11,13-14,21-29,31-36H,12,15-20H2,1-3H3/b5-4+,8-6+,9-7+,13-10+,14-11+/t21-,22+,23-,24+,25-,26+,27+,28-,29+/m0/s1
InChI Key XZNYCRZDVXCORM-LWYGBUOPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48O8
Molecular Weight 536.70 g/mol
Exact Mass 536.33491849 g/mol
Topological Polar Surface Area (TPSA) 148.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 2.88
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,4R,6R,10S,12S,14S,16S,17E,19E,21E,23E,25E,27S,28S)-4,6,10,12,14,16-hexahydroxy-3,27,28-trimethyl-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 + 0.8508 85.08%
Caco-2 - 0.7965 79.65%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7333 73.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8716 87.16%
OATP1B3 inhibitior + 0.9436 94.36%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7563 75.63%
P-glycoprotein inhibitior - 0.5652 56.52%
P-glycoprotein substrate - 0.7431 74.31%
CYP3A4 substrate + 0.5699 56.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8752 87.52%
CYP3A4 inhibition - 0.7144 71.44%
CYP2C9 inhibition - 0.9235 92.35%
CYP2C19 inhibition - 0.8461 84.61%
CYP2D6 inhibition - 0.9502 95.02%
CYP1A2 inhibition - 0.8720 87.20%
CYP2C8 inhibition - 0.9364 93.64%
CYP inhibitory promiscuity - 0.9732 97.32%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9328 93.28%
Carcinogenicity (trinary) Non-required 0.7405 74.05%
Eye corrosion - 0.9499 94.99%
Eye irritation - 0.9496 94.96%
Skin irritation - 0.5851 58.51%
Skin corrosion - 0.9367 93.67%
Ames mutagenesis - 0.7174 71.74%
Human Ether-a-go-go-Related Gene inhibition + 0.8683 86.83%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.7198 71.98%
skin sensitisation - 0.8491 84.91%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.6801 68.01%
Acute Oral Toxicity (c) III 0.5276 52.76%
Estrogen receptor binding + 0.7840 78.40%
Androgen receptor binding - 0.5335 53.35%
Thyroid receptor binding + 0.5441 54.41%
Glucocorticoid receptor binding + 0.6157 61.57%
Aromatase binding - 0.5388 53.88%
PPAR gamma + 0.5184 51.84%
Honey bee toxicity - 0.8723 87.23%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.8221 82.21%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.87% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.55% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.38% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.22% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.18% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.14% 91.11%
CHEMBL2581 P07339 Cathepsin D 84.50% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.85% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.40% 99.23%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.13% 92.94%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.56% 89.00%

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 162891131
LOTUS LTS0164549
wikiData Q105345065