Cinatrin A

Details

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Internal ID 6c5e7a9f-adec-4f20-b6d7-833f11a00453
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name (3R,5R)-8-dec-9-enyl-3,4-dihydroxy-2,6-dioxo-1,7-dioxaspiro[4.4]nonane-4-carboxylic acid
SMILES (Canonical) C=CCCCCCCCCC1CC2(C(=O)O1)C(C(C(=O)O2)O)(C(=O)O)O
SMILES (Isomeric) C=CCCCCCCCCC1C[C@]2(C(=O)O1)C([C@H](C(=O)O2)O)(C(=O)O)O
InChI InChI=1S/C18H26O8/c1-2-3-4-5-6-7-8-9-10-12-11-17(16(23)25-12)18(24,15(21)22)13(19)14(20)26-17/h2,12-13,19,24H,1,3-11H2,(H,21,22)/t12?,13-,17-,18?/m0/s1
InChI Key ZFUPZDZSERSKNA-ZVRZEWSUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H26O8
Molecular Weight 370.40 g/mol
Exact Mass 370.16276778 g/mol
Topological Polar Surface Area (TPSA) 130.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 1.08
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 10

Synonyms

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136266-33-6
(3R,5R)-8-dec-9-enyl-3,4-dihydroxy-2,6-dioxo-1,7-dioxaspiro[4.4]nonane-4-carboxylic acid
DTXSID20929305
8-(Dec-9-en-1-yl)-3,4-dihydroxy-2,6-dioxo-1,7-dioxaspiro[4.4]nonane-4-carboxylic acid
1,7-Dioxaspiro(4.4)nonane-4-carboxylic acid, 8-(9-decenyl)-3,4-dihydroxy-2,6-dioxo-, (3R-(3alpha,4beta,5beta(R*)))-

2D Structure

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2D Structure of Cinatrin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5794 57.94%
Caco-2 - 0.8150 81.50%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7642 76.42%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.9149 91.49%
OATP1B3 inhibitior + 0.9337 93.37%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8541 85.41%
P-glycoprotein inhibitior - 0.7560 75.60%
P-glycoprotein substrate - 0.7185 71.85%
CYP3A4 substrate + 0.5727 57.27%
CYP2C9 substrate - 0.6047 60.47%
CYP2D6 substrate - 0.8552 85.52%
CYP3A4 inhibition - 0.8760 87.60%
CYP2C9 inhibition - 0.9054 90.54%
CYP2C19 inhibition - 0.8621 86.21%
CYP2D6 inhibition - 0.9469 94.69%
CYP1A2 inhibition - 0.8952 89.52%
CYP2C8 inhibition - 0.6998 69.98%
CYP inhibitory promiscuity - 0.9905 99.05%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9543 95.43%
Carcinogenicity (trinary) Non-required 0.5994 59.94%
Eye corrosion - 0.9689 96.89%
Eye irritation - 0.8103 81.03%
Skin irritation - 0.6837 68.37%
Skin corrosion - 0.8965 89.65%
Ames mutagenesis - 0.6737 67.37%
Human Ether-a-go-go-Related Gene inhibition - 0.4681 46.81%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.5073 50.73%
skin sensitisation - 0.8526 85.26%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.7109 71.09%
Acute Oral Toxicity (c) III 0.5006 50.06%
Estrogen receptor binding + 0.7649 76.49%
Androgen receptor binding + 0.6626 66.26%
Thyroid receptor binding + 0.5794 57.94%
Glucocorticoid receptor binding + 0.7289 72.89%
Aromatase binding - 0.5244 52.44%
PPAR gamma + 0.7228 72.28%
Honey bee toxicity - 0.8928 89.28%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5724 57.24%
Fish aquatic toxicity + 0.8841 88.41%

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 95.46% 91.11%
CHEMBL1829 O15379 Histone deacetylase 3 93.90% 95.00%
CHEMBL221 P23219 Cyclooxygenase-1 87.49% 90.17%
CHEMBL1937 Q92769 Histone deacetylase 2 87.11% 94.75%
CHEMBL230 P35354 Cyclooxygenase-2 84.94% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.92% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.77% 99.17%
CHEMBL325 Q13547 Histone deacetylase 1 83.49% 95.92%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.08% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.80% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.51% 89.34%
CHEMBL4530 P00488 Coagulation factor XIII 82.03% 96.00%
CHEMBL340 P08684 Cytochrome P450 3A4 81.84% 91.19%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.60% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.17% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.71% 97.09%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.33% 93.00%

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 131943
LOTUS LTS0210240
wikiData Q82904143