(2R)-2,3-diamino-3-oxopropane-1-sulfonic acid

Details

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Internal ID b4d1df97-111c-450f-950d-6b9c0316b053
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acid amides
IUPAC Name (2R)-2,3-diamino-3-oxopropane-1-sulfonic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C3H8N2O4S/c4-2(3(5)6)1-10(7,8)9/h2H,1,4H2,(H2,5,6)(H,7,8,9)/t2-/m0/s1
InChI Key QJUICSCUFJBBDE-REOHCLBHSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C3H8N2O4S
Molecular Weight 168.17 g/mol
Exact Mass 168.02047791 g/mol
Topological Polar Surface Area (TPSA) 132.00 Ų
XlogP -5.10
Atomic LogP (AlogP) -2.31
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R)-2,3-diamino-3-oxopropane-1-sulfonic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9318 93.18%
Caco-2 - 0.8365 83.65%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.9000 90.00%
Subcellular localzation Mitochondria 0.5135 51.35%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.9789 97.89%
OATP1B3 inhibitior + 0.9416 94.16%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9452 94.52%
P-glycoprotein inhibitior - 0.9777 97.77%
P-glycoprotein substrate - 0.9727 97.27%
CYP3A4 substrate - 0.7565 75.65%
CYP2C9 substrate - 0.8141 81.41%
CYP2D6 substrate - 0.7931 79.31%
CYP3A4 inhibition - 0.9673 96.73%
CYP2C9 inhibition - 0.8707 87.07%
CYP2C19 inhibition - 0.8601 86.01%
CYP2D6 inhibition - 0.9218 92.18%
CYP1A2 inhibition - 0.8657 86.57%
CYP2C8 inhibition - 0.9879 98.79%
CYP inhibitory promiscuity - 0.9938 99.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.7015 70.15%
Eye corrosion - 0.8431 84.31%
Eye irritation - 0.5659 56.59%
Skin irritation - 0.7523 75.23%
Skin corrosion - 0.8877 88.77%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8283 82.83%
Micronuclear + 0.8700 87.00%
Hepatotoxicity + 0.6430 64.30%
skin sensitisation - 0.8581 85.81%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7283 72.83%
Acute Oral Toxicity (c) III 0.5579 55.79%
Estrogen receptor binding - 0.9177 91.77%
Androgen receptor binding - 0.7908 79.08%
Thyroid receptor binding - 0.8236 82.36%
Glucocorticoid receptor binding - 0.8229 82.29%
Aromatase binding - 0.9392 93.92%
PPAR gamma - 0.7020 70.20%
Honey bee toxicity - 0.8431 84.31%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity - 0.7923 79.23%

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 92.07% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.39% 97.21%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 87.27% 92.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.14% 96.95%
CHEMBL340 P08684 Cytochrome P450 3A4 84.16% 91.19%

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 54231775
LOTUS LTS0008701
wikiData Q105222880