7-Chloro-indole-1-acetic acid

Details

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Internal ID 30d0eabc-f759-4ea8-be5c-e62dfa59ddb4
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indolyl carboxylic acids and derivatives
IUPAC Name 2-(7-chloroindol-1-yl)acetic acid
SMILES (Canonical) C1=CC2=C(C(=C1)Cl)N(C=C2)CC(=O)O
SMILES (Isomeric) C1=CC2=C(C(=C1)Cl)N(C=C2)CC(=O)O
InChI InChI=1S/C10H8ClNO2/c11-8-3-1-2-7-4-5-12(10(7)8)6-9(13)14/h1-5H,6H2,(H,13,14)
InChI Key HCPLEHHIQHALRW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H8ClNO2
Molecular Weight 209.63 g/mol
Exact Mass 209.0243562 g/mol
Topological Polar Surface Area (TPSA) 42.20 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.38
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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943654-32-8
2-(7-chloro-1h-indol-1-yl)acetic acid
SCHEMBL1576332
HCPLEHHIQHALRW-UHFFFAOYSA-N
F80707

2D Structure

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2D Structure of 7-Chloro-indole-1-acetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.9586 95.86%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.4784 47.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9527 95.27%
OATP1B3 inhibitior + 0.9474 94.74%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6817 68.17%
BSEP inhibitior - 0.8313 83.13%
P-glycoprotein inhibitior - 0.9835 98.35%
P-glycoprotein substrate - 0.9805 98.05%
CYP3A4 substrate - 0.6503 65.03%
CYP2C9 substrate - 0.7939 79.39%
CYP2D6 substrate - 0.8840 88.40%
CYP3A4 inhibition - 0.9607 96.07%
CYP2C9 inhibition - 0.8683 86.83%
CYP2C19 inhibition - 0.8841 88.41%
CYP2D6 inhibition - 0.9357 93.57%
CYP1A2 inhibition - 0.6479 64.79%
CYP2C8 inhibition - 0.7840 78.40%
CYP inhibitory promiscuity - 0.8158 81.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8121 81.21%
Carcinogenicity (trinary) Non-required 0.5356 53.56%
Eye corrosion - 0.9709 97.09%
Eye irritation + 0.8505 85.05%
Skin irritation - 0.7348 73.48%
Skin corrosion - 0.9046 90.46%
Ames mutagenesis - 0.7954 79.54%
Human Ether-a-go-go-Related Gene inhibition - 0.8792 87.92%
Micronuclear + 0.6074 60.74%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.8803 88.03%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5577 55.77%
Acute Oral Toxicity (c) III 0.6142 61.42%
Estrogen receptor binding - 0.9317 93.17%
Androgen receptor binding - 0.5545 55.45%
Thyroid receptor binding - 0.8071 80.71%
Glucocorticoid receptor binding + 0.5377 53.77%
Aromatase binding - 0.6618 66.18%
PPAR gamma + 0.6983 69.83%
Honey bee toxicity - 0.9888 98.88%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5971 59.71%
Fish aquatic toxicity - 0.4537 45.37%

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
CHEMBL221 P23219 Cyclooxygenase-1 97.44% 90.17%
CHEMBL2581 P07339 Cathepsin D 92.35% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.34% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.36% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.06% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 83.51% 89.63%

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.
Aglaia tomentosa
Backhousia citriodora
Capraria biflora
Centipeda minima
Mentha suaveolens subsp. timija
Senecio macrocephalus
Upuna borneensis

Cross-Links

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PubChem 67082699
NPASS NPC140751