Mitraphyllic acid

Details

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Internal ID da933696-f581-4479-8885-3433a1fbff4c
Taxonomy Organoheterocyclic compounds > Indolizidines
IUPAC Name (1S,4aS,5aS,6R,10aR)-1-methyl-2'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylic acid
SMILES (Canonical) CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)O)C5=CC=CC=C5NC4=O
SMILES (Isomeric) C[C@H]1[C@H]2CN3CC[C@]4([C@@H]3C[C@@H]2C(=CO1)C(=O)O)C5=CC=CC=C5NC4=O
InChI InChI=1S/C20H22N2O4/c1-11-13-9-22-7-6-20(15-4-2-3-5-16(15)21-19(20)25)17(22)8-12(13)14(10-26-11)18(23)24/h2-5,10-13,17H,6-9H2,1H3,(H,21,25)(H,23,24)/t11-,12-,13+,17-,20+/m0/s1
InChI Key BLXUPISDXRFTCK-GALDEACFSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H22N2O4
Molecular Weight 354.40 g/mol
Exact Mass 354.15795719 g/mol
Topological Polar Surface Area (TPSA) 78.90 Ų
XlogP -1.00
Atomic LogP (AlogP) 1.97
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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10126-00-8
Isomitraphyllic acid
DTXSID80906031
(1S,4aS,5aS,6R,10aR)-1-methyl-2'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylic acid
Formosanan-16-carboxylic acid, 19-methyl-2-oxo-, (19alpha)-
2-Hydroxy-19-methyl-1,2-didehydroformosanan-16-carboxylic acid

2D Structure

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2D Structure of Mitraphyllic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9317 93.17%
Caco-2 + 0.5128 51.28%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7304 73.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8718 87.18%
OATP1B3 inhibitior + 0.9310 93.10%
MATE1 inhibitior - 0.8409 84.09%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6349 63.49%
P-glycoprotein inhibitior - 0.7003 70.03%
P-glycoprotein substrate - 0.5282 52.82%
CYP3A4 substrate + 0.6488 64.88%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.7709 77.09%
CYP3A4 inhibition - 0.8354 83.54%
CYP2C9 inhibition - 0.7652 76.52%
CYP2C19 inhibition - 0.7868 78.68%
CYP2D6 inhibition - 0.8795 87.95%
CYP1A2 inhibition - 0.7800 78.00%
CYP2C8 inhibition - 0.5757 57.57%
CYP inhibitory promiscuity - 0.9172 91.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5326 53.26%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.9957 99.57%
Skin irritation - 0.7764 77.64%
Skin corrosion - 0.9351 93.51%
Ames mutagenesis - 0.6844 68.44%
Human Ether-a-go-go-Related Gene inhibition + 0.6800 68.00%
Micronuclear + 0.8000 80.00%
Hepatotoxicity + 0.6406 64.06%
skin sensitisation - 0.8476 84.76%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.5630 56.30%
Acute Oral Toxicity (c) III 0.5673 56.73%
Estrogen receptor binding + 0.7981 79.81%
Androgen receptor binding + 0.7152 71.52%
Thyroid receptor binding - 0.5830 58.30%
Glucocorticoid receptor binding + 0.5576 55.76%
Aromatase binding - 0.5430 54.30%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.8788 87.88%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9751 97.51%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.81% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.83% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.16% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.49% 99.23%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 92.12% 94.08%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.01% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.95% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.19% 90.71%
CHEMBL2581 P07339 Cathepsin D 85.07% 98.95%
CHEMBL238 Q01959 Dopamine transporter 84.98% 95.88%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.88% 94.62%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.35% 93.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.27% 93.03%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.19% 97.09%
CHEMBL4208 P20618 Proteasome component C5 84.15% 90.00%
CHEMBL5028 O14672 ADAM10 83.48% 97.50%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.37% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Cryptotaenia japonica
Uncaria sinensis

Cross-Links

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PubChem 193449
NPASS NPC280348
LOTUS LTS0176506
wikiData Q82874691