3-Sulfopropanoic acid

Details

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Internal ID 5e00f4f3-f7b8-48e7-93bd-b038b4f7297c
Taxonomy Organic acids and derivatives > Organic sulfonic acids and derivatives > Organosulfonic acids and derivatives > Organosulfonic acids
IUPAC Name 3-sulfopropanoic acid
SMILES (Canonical) C(CS(=O)(=O)O)C(=O)O
SMILES (Isomeric) C(CS(=O)(=O)O)C(=O)O
InChI InChI=1S/C3H6O5S/c4-3(5)1-2-9(6,7)8/h1-2H2,(H,4,5)(H,6,7,8)
InChI Key OURSFPZPOXNNKX-UHFFFAOYSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C3H6O5S
Molecular Weight 154.14 g/mol
Exact Mass 153.99359446 g/mol
Topological Polar Surface Area (TPSA) 100.00 Ų
XlogP -1.40
Atomic LogP (AlogP) -0.65
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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Propanoic acid, 3-sulfo-
44826-45-1
3-sulfopropionic acid
6306-41-8
CI1QNB6JPX
NSC22947
NSC-22947
3-Sulfopropanoicacid
NSC 22947
UNII-CI1QNB6JPX
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Sulfopropanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8122 81.22%
Caco-2 - 0.5361 53.61%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.6649 66.49%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9544 95.44%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9760 97.60%
P-glycoprotein inhibitior - 0.9807 98.07%
P-glycoprotein substrate - 0.9921 99.21%
CYP3A4 substrate - 0.7644 76.44%
CYP2C9 substrate + 0.6131 61.31%
CYP2D6 substrate - 0.8673 86.73%
CYP3A4 inhibition - 0.9927 99.27%
CYP2C9 inhibition - 0.9164 91.64%
CYP2C19 inhibition - 0.9174 91.74%
CYP2D6 inhibition - 0.9277 92.77%
CYP1A2 inhibition - 0.8836 88.36%
CYP2C8 inhibition - 0.9820 98.20%
CYP inhibitory promiscuity - 0.9926 99.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7131 71.31%
Carcinogenicity (trinary) Non-required 0.7034 70.34%
Eye corrosion + 0.6478 64.78%
Eye irritation + 0.7476 74.76%
Skin irritation - 0.6708 67.08%
Skin corrosion + 0.7347 73.47%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7719 77.19%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.5680 56.80%
skin sensitisation - 0.6225 62.25%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7037 70.37%
Acute Oral Toxicity (c) III 0.7251 72.51%
Estrogen receptor binding - 0.9382 93.82%
Androgen receptor binding - 0.9394 93.94%
Thyroid receptor binding - 0.8893 88.93%
Glucocorticoid receptor binding - 0.9176 91.76%
Aromatase binding - 0.8973 89.73%
PPAR gamma - 0.7668 76.68%
Honey bee toxicity - 0.9068 90.68%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.7139 71.39%

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 87.36% 96.09%
CHEMBL2581 P07339 Cathepsin D 84.19% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 84.12% 83.82%

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.
There are no matching plants.

Cross-Links

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PubChem 409694
LOTUS LTS0218445
wikiData Q27144346