Pinnaic acid

Details

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Internal ID 81f982fc-d8ad-4507-8226-e4ee5a1995d1
Taxonomy Organoheterocyclic compounds > Azaspirodecane derivatives
IUPAC Name (E)-4-[(4R,5S,7R)-4-[(2S,3E,5R,6Z)-7-chloro-5,9-dihydroxynona-3,6-dien-2-yl]-6-azaspiro[4.5]decan-7-yl]-2-methylbut-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H36ClNO4/c1-16(8-10-20(27)15-18(24)11-14-26)21-6-4-13-23(21)12-3-5-19(25-23)9-7-17(2)22(28)29/h7-8,10,15-16,19-21,25-27H,3-6,9,11-14H2,1-2H3,(H,28,29)/b10-8+,17-7+,18-15-/t16-,19+,20+,21+,23+/m0/s1
InChI Key AASNHMKFRLWUOJ-IBSBDYNISA-N
Popularity 18 references in papers

Physical and Chemical Properties

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Molecular Formula C23H36ClNO4
Molecular Weight 426.00 g/mol
Exact Mass 425.2332863 g/mol
Topological Polar Surface Area (TPSA) 89.80 Ų
XlogP 1.20
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 9

Synonyms

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RefChem:929299
(E)-4-((4R,5S,7R)-4-((2S,3E,5R,6Z)-7-chloro-5,9-dihydroxynona-3,6-dien-2-yl)-6-azaspiro(4.5)decan-7-yl)-2-methylbut-2-enoic acid
(E)-4-((4R,5S,7R)-4-((2S,3E,5R,6Z)-7-chloro-5,9-dihydroxynona-3,6-dien-2-yl)-6-azoniaspiro(4.5)decan-7-yl)-2-methylbut-2-enoate
(E)-4-((4S,5R,7S)-4-((2S,3E,6Z)-7-chloro-5,9-dihydroxynona-3,6-dien-2-yl)-6-azaspiro(4.5)decan-7-yl)-2-methylbut-2-enoic acid

2D Structure

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2D Structure of Pinnaic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9866 98.66%
Caco-2 - 0.7647 76.47%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6095 60.95%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8535 85.35%
OATP1B3 inhibitior + 0.9341 93.41%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5776 57.76%
BSEP inhibitior - 0.4636 46.36%
P-glycoprotein inhibitior - 0.6192 61.92%
P-glycoprotein substrate + 0.5060 50.60%
CYP3A4 substrate + 0.6447 64.47%
CYP2C9 substrate - 0.8018 80.18%
CYP2D6 substrate - 0.8525 85.25%
CYP3A4 inhibition - 0.9090 90.90%
CYP2C9 inhibition - 0.8025 80.25%
CYP2C19 inhibition - 0.8495 84.95%
CYP2D6 inhibition - 0.8546 85.46%
CYP1A2 inhibition - 0.8115 81.15%
CYP2C8 inhibition - 0.5917 59.17%
CYP inhibitory promiscuity - 0.9050 90.50%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8356 83.56%
Carcinogenicity (trinary) Non-required 0.6498 64.98%
Eye corrosion - 0.9852 98.52%
Eye irritation - 0.9835 98.35%
Skin irritation - 0.7278 72.78%
Skin corrosion - 0.9177 91.77%
Ames mutagenesis + 0.5186 51.86%
Human Ether-a-go-go-Related Gene inhibition + 0.8144 81.44%
Micronuclear - 0.6100 61.00%
Hepatotoxicity - 0.5407 54.07%
skin sensitisation - 0.7893 78.93%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.6683 66.83%
Acute Oral Toxicity (c) III 0.6042 60.42%
Estrogen receptor binding + 0.8150 81.50%
Androgen receptor binding + 0.6130 61.30%
Thyroid receptor binding + 0.6663 66.63%
Glucocorticoid receptor binding + 0.6213 62.13%
Aromatase binding + 0.5399 53.99%
PPAR gamma + 0.6474 64.74%
Honey bee toxicity - 0.7523 75.23%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6852 68.52%
Fish aquatic toxicity + 0.6771 67.71%

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 99.56% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.88% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.26% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.43% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.67% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.62% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 91.29% 91.19%
CHEMBL218 P21554 Cannabinoid CB1 receptor 90.86% 96.61%
CHEMBL4227 P25090 Lipoxin A4 receptor 90.24% 100.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 90.20% 93.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 89.47% 95.50%
CHEMBL284 P27487 Dipeptidyl peptidase IV 89.32% 95.69%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 87.54% 98.75%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 86.87% 96.47%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 86.05% 96.38%
CHEMBL1937 Q92769 Histone deacetylase 2 85.86% 94.75%
CHEMBL237 P41145 Kappa opioid receptor 85.68% 98.10%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 84.92% 96.03%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 83.61% 92.88%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.42% 96.21%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.60% 93.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.58% 93.04%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.75% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.42% 96.77%
CHEMBL5255 O00206 Toll-like receptor 4 80.02% 92.50%

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 9979869
LOTUS LTS0099963
wikiData Q104908332