(S,S)-Tartrate

Details

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Internal ID 201508fd-7552-4d54-aef9-4b8578ade977
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Beta hydroxy acids and derivatives
IUPAC Name (2S,3S)-2,3-dihydroxybutanedioate
SMILES (Canonical) C(C(C(=O)[O-])O)(C(=O)[O-])O
SMILES (Isomeric) [C@H]([C@@H](C(=O)[O-])O)(C(=O)[O-])O
InChI InChI=1S/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10)/p-2/t1-,2-/m0/s1
InChI Key FEWJPZIEWOKRBE-LWMBPPNESA-L
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C4H4O6-2
Molecular Weight 148.07 g/mol
Exact Mass 148.00078784 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP -0.60
Atomic LogP (AlogP) -4.79
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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D-Tartrate
(2S,3S)-2,3-dihydroxybutanedioate
(-)-tartrate
D-tartrate(2-)
(2S,3S)-tartrate
D-tartarate
D-threarate
(D)-Tartrate
D-(-)-tartrate
(?)-D-Tartrate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (S,S)-Tartrate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5536 55.36%
Caco-2 - 0.9768 97.68%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7522 75.22%
OATP2B1 inhibitior - 0.8610 86.10%
OATP1B1 inhibitior + 0.9794 97.94%
OATP1B3 inhibitior + 0.9649 96.49%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9812 98.12%
P-glycoprotein inhibitior - 0.9755 97.55%
P-glycoprotein substrate - 0.9965 99.65%
CYP3A4 substrate - 0.8261 82.61%
CYP2C9 substrate - 0.6062 60.62%
CYP2D6 substrate - 0.8689 86.89%
CYP3A4 inhibition - 0.9461 94.61%
CYP2C9 inhibition - 0.9257 92.57%
CYP2C19 inhibition - 0.9649 96.49%
CYP2D6 inhibition - 0.9476 94.76%
CYP1A2 inhibition - 0.9351 93.51%
CYP2C8 inhibition - 0.9967 99.67%
CYP inhibitory promiscuity - 0.9930 99.30%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.5196 51.96%
Carcinogenicity (trinary) Non-required 0.7308 73.08%
Eye corrosion - 0.7823 78.23%
Eye irritation + 0.6353 63.53%
Skin irritation + 0.5657 56.57%
Skin corrosion - 0.8774 87.74%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8485 84.85%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.7300 73.00%
skin sensitisation - 0.9167 91.67%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7016 70.16%
Estrogen receptor binding - 0.8274 82.74%
Androgen receptor binding - 0.8527 85.27%
Thyroid receptor binding - 0.7707 77.07%
Glucocorticoid receptor binding - 0.7731 77.31%
Aromatase binding - 0.8169 81.69%
PPAR gamma - 0.7357 73.57%
Honey bee toxicity - 0.8937 89.37%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity - 0.5489 54.89%

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
CHEMBL4040 P28482 MAP kinase ERK2 90.64% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.22% 96.09%

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.
Aloe africana
Aloe ferox
Aloe spicata
Aloe vera
Cornus officinalis
Hippophae rhamnoides
Pogostemon cablin
Prunus mume

Cross-Links

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PubChem 5460284
NPASS NPC100749