(2Z,5R,6E,8R,9R,12Z,14Z)-15-cyclohexyl-4-(dimethylamino)-5,8,11-trihydroxy-8-methyl-9-phosphonooxypentadeca-2,6,12,14-tetraenoic acid

Details

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Internal ID 60eba0c2-6796-4779-ba29-fa7bae1bfad4
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (2Z,5R,6E,8R,9R,12Z,14Z)-15-cyclohexyl-4-(dimethylamino)-5,8,11-trihydroxy-8-methyl-9-phosphonooxypentadeca-2,6,12,14-tetraenoic acid
SMILES (Canonical) CC(C=CC(C(C=CC(=O)O)N(C)C)O)(C(CC(C=CC=CC1CCCCC1)O)OP(=O)(O)O)O
SMILES (Isomeric) C[C@@](/C=C/[C@H](C(/C=C\C(=O)O)N(C)C)O)([C@@H](CC(/C=C\C=C/C1CCCCC1)O)OP(=O)(O)O)O
InChI InChI=1S/C24H40NO9P/c1-24(30,16-15-21(27)20(25(2)3)13-14-23(28)29)22(34-35(31,32)33)17-19(26)12-8-7-11-18-9-5-4-6-10-18/h7-8,11-16,18-22,26-27,30H,4-6,9-10,17H2,1-3H3,(H,28,29)(H2,31,32,33)/b11-7-,12-8-,14-13-,16-15+/t19?,20?,21-,22-,24-/m1/s1
InChI Key JQMRWKPAJQOQLP-ODPXWWGOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H40NO9P
Molecular Weight 517.50 g/mol
Exact Mass 517.24406885 g/mol
Topological Polar Surface Area (TPSA) 168.00 Ų
XlogP -1.30
Atomic LogP (AlogP) 2.15
H-Bond Acceptor 7
H-Bond Donor 6
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2Z,5R,6E,8R,9R,12Z,14Z)-15-cyclohexyl-4-(dimethylamino)-5,8,11-trihydroxy-8-methyl-9-phosphonooxypentadeca-2,6,12,14-tetraenoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6619 66.19%
Caco-2 - 0.8270 82.70%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.6879 68.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8823 88.23%
OATP1B3 inhibitior + 0.9338 93.38%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5545 55.45%
P-glycoprotein inhibitior - 0.4421 44.21%
P-glycoprotein substrate - 0.5076 50.76%
CYP3A4 substrate + 0.6776 67.76%
CYP2C9 substrate - 0.8018 80.18%
CYP2D6 substrate - 0.8357 83.57%
CYP3A4 inhibition - 0.9104 91.04%
CYP2C9 inhibition - 0.7880 78.80%
CYP2C19 inhibition - 0.7510 75.10%
CYP2D6 inhibition - 0.8809 88.09%
CYP1A2 inhibition - 0.7895 78.95%
CYP2C8 inhibition + 0.4903 49.03%
CYP inhibitory promiscuity - 0.9564 95.64%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7428 74.28%
Carcinogenicity (trinary) Non-required 0.5852 58.52%
Eye corrosion - 0.9564 95.64%
Eye irritation - 0.9408 94.08%
Skin irritation - 0.7628 76.28%
Skin corrosion - 0.9002 90.02%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6704 67.04%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8157 81.57%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6693 66.93%
Acute Oral Toxicity (c) III 0.5393 53.93%
Estrogen receptor binding + 0.6345 63.45%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.5899 58.99%
Glucocorticoid receptor binding + 0.5447 54.47%
Aromatase binding + 0.5557 55.57%
PPAR gamma + 0.5816 58.16%
Honey bee toxicity - 0.6642 66.42%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9031 90.31%

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 99.33% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.43% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.34% 98.95%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 91.88% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.72% 93.56%
CHEMBL237 P41145 Kappa opioid receptor 91.24% 98.10%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 90.86% 95.17%
CHEMBL5255 O00206 Toll-like receptor 4 90.59% 92.50%
CHEMBL340 P08684 Cytochrome P450 3A4 90.26% 91.19%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 87.88% 96.38%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 86.65% 96.47%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.63% 99.17%
CHEMBL206 P03372 Estrogen receptor alpha 85.68% 97.64%
CHEMBL4227 P25090 Lipoxin A4 receptor 85.46% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 84.85% 96.61%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 84.52% 94.01%
CHEMBL2413 P32246 C-C chemokine receptor type 1 83.59% 89.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.22% 94.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.10% 93.00%
CHEMBL2179 P04062 Beta-glucocerebrosidase 82.88% 85.31%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.87% 97.29%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.50% 97.09%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 81.71% 97.47%
CHEMBL2061 P19793 Retinoid X receptor alpha 81.62% 91.67%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.61% 97.50%
CHEMBL4662 P28074 Proteasome Macropain subunit MB1 80.87% 93.85%

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 162980119
LOTUS LTS0056901
wikiData Q105133548