Ramalinic acid A

Details

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Internal ID a7b53f33-7866-4d4c-bf2d-b12f145d9cd6
Taxonomy Lignans, neolignans and related compounds
IUPAC Name 3-(2-carboxy-5-methoxy-3-propylphenoxy)-2-hydroxy-4-methoxy-6-propylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H26O8/c1-5-7-12-9-14(28-3)11-15(17(12)21(24)25)30-20-16(29-4)10-13(8-6-2)18(19(20)23)22(26)27/h9-11,23H,5-8H2,1-4H3,(H,24,25)(H,26,27)
InChI Key XIJCKILIISXBES-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O8
Molecular Weight 418.40 g/mol
Exact Mass 418.16276778 g/mol
Topological Polar Surface Area (TPSA) 123.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.50
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 10

Synonyms

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RefChem:178597
CHEBI:200286
3-(2-carboxy-5-methoxy-3-propylphenoxy)-2-hydroxy-4-methoxy-6-propylbenzoic acid

2D Structure

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2D Structure of Ramalinic acid A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8194 81.94%
Caco-2 + 0.6456 64.56%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8308 83.08%
OATP2B1 inhibitior - 0.8622 86.22%
OATP1B1 inhibitior + 0.8322 83.22%
OATP1B3 inhibitior - 0.2162 21.62%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9051 90.51%
P-glycoprotein inhibitior + 0.6499 64.99%
P-glycoprotein substrate - 0.7799 77.99%
CYP3A4 substrate - 0.5373 53.73%
CYP2C9 substrate - 0.6306 63.06%
CYP2D6 substrate - 0.8730 87.30%
CYP3A4 inhibition - 0.7896 78.96%
CYP2C9 inhibition + 0.6415 64.15%
CYP2C19 inhibition - 0.6218 62.18%
CYP2D6 inhibition - 0.7898 78.98%
CYP1A2 inhibition + 0.5556 55.56%
CYP2C8 inhibition + 0.7392 73.92%
CYP inhibitory promiscuity - 0.6382 63.82%
UGT catelyzed + 0.5362 53.62%
Carcinogenicity (binary) - 0.7676 76.76%
Carcinogenicity (trinary) Non-required 0.7082 70.82%
Eye corrosion - 0.9862 98.62%
Eye irritation - 0.5773 57.73%
Skin irritation - 0.8364 83.64%
Skin corrosion - 0.8961 89.61%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4661 46.61%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.5533 55.33%
skin sensitisation - 0.8889 88.89%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.5503 55.03%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.5709 57.09%
Acute Oral Toxicity (c) III 0.5407 54.07%
Estrogen receptor binding + 0.8131 81.31%
Androgen receptor binding - 0.5308 53.08%
Thyroid receptor binding - 0.5127 51.27%
Glucocorticoid receptor binding + 0.7093 70.93%
Aromatase binding + 0.5452 54.52%
PPAR gamma + 0.7837 78.37%
Honey bee toxicity - 0.9441 94.41%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9903 99.03%

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 96.65% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.22% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.41% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.55% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.89% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.15% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.27% 96.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.23% 95.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.06% 95.50%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 86.88% 94.42%
CHEMBL2535 P11166 Glucose transporter 86.74% 98.75%
CHEMBL4208 P20618 Proteasome component C5 85.47% 90.00%
CHEMBL1255126 O15151 Protein Mdm4 84.52% 90.20%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.76% 92.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.87% 99.15%
CHEMBL3194 P02766 Transthyretin 81.78% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.74% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.31% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.57% 97.21%

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 102531719
LOTUS LTS0048400
wikiData Q75070126