Arctic acid C

Details

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Internal ID 069abcee-8aa6-4ab8-9581-25fea7235c12
Taxonomy Organoheterocyclic compounds > Bi- and oligothiophenes
IUPAC Name 2-hydroxy-2-[5-(5-prop-1-ynylthiophen-2-yl)thiophen-2-yl]acetic acid
SMILES (Canonical) CC#CC1=CC=C(S1)C2=CC=C(S2)C(C(=O)O)O
SMILES (Isomeric) CC#CC1=CC=C(S1)C2=CC=C(S2)C(C(=O)O)O
InChI InChI=1S/C13H10O3S2/c1-2-3-8-4-5-9(17-8)10-6-7-11(18-10)12(14)13(15)16/h4-7,12,14H,1H3,(H,15,16)
InChI Key YUIKESNQNJLOMW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H10O3S2
Molecular Weight 278.40 g/mol
Exact Mass 278.00713652 g/mol
Topological Polar Surface Area (TPSA) 114.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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UNII-E8I75C0IAK
E8I75C0IAK
102054-35-3
(2,2'-Bithiophene)-5-acetic acid, alpha-hydroxy-5'-(1-propynyl)-
Q27277000
(2,2'-BITHIOPHENE)-5-ACETIC ACID, .ALPHA.-HYDROXY-5'-(1-PROPYNYL)-

2D Structure

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2D Structure of Arctic acid C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9588 95.88%
Caco-2 - 0.5719 57.19%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8118 81.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9398 93.98%
OATP1B3 inhibitior + 0.9305 93.05%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8703 87.03%
P-glycoprotein inhibitior - 0.9597 95.97%
P-glycoprotein substrate - 0.9359 93.59%
CYP3A4 substrate - 0.6254 62.54%
CYP2C9 substrate + 0.8042 80.42%
CYP2D6 substrate - 0.8568 85.68%
CYP3A4 inhibition - 0.9081 90.81%
CYP2C9 inhibition - 0.5746 57.46%
CYP2C19 inhibition - 0.7777 77.77%
CYP2D6 inhibition - 0.9146 91.46%
CYP1A2 inhibition - 0.7674 76.74%
CYP2C8 inhibition - 0.8976 89.76%
CYP inhibitory promiscuity - 0.6344 63.44%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7417 74.17%
Carcinogenicity (trinary) Non-required 0.5200 52.00%
Eye corrosion - 0.9564 95.64%
Eye irritation - 0.8835 88.35%
Skin irritation - 0.7235 72.35%
Skin corrosion - 0.8443 84.43%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6187 61.87%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation - 0.7200 72.00%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.7443 74.43%
Acute Oral Toxicity (c) III 0.5013 50.13%
Estrogen receptor binding + 0.7288 72.88%
Androgen receptor binding + 0.5947 59.47%
Thyroid receptor binding + 0.5771 57.71%
Glucocorticoid receptor binding + 0.7927 79.27%
Aromatase binding + 0.8102 81.02%
PPAR gamma + 0.6048 60.48%
Honey bee toxicity - 0.9416 94.16%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9174 91.74%

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 94.25% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.60% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.20% 95.56%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.94% 94.08%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.55% 85.30%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.94% 95.50%
CHEMBL4208 P20618 Proteasome component C5 80.70% 90.00%
CHEMBL221 P23219 Cyclooxygenase-1 80.34% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.29% 96.00%

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.
Arctium lappa

Cross-Links

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PubChem 71587384
LOTUS LTS0139168
wikiData Q27277000