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D-Lactic Acid - >90.0%(T), high purity , CAS No.10326-41-7, Agonist of HCA 1 receptor

Moligand™
≥90%(T)

CAS#: 10326-41-7
Formula: C₃H₆O₃
Molecular Weight: 90.08
MDL number: MFCD00068311
PubChem CID: 61503

Item Number

S161106

Grouped product items
SKU	Size	Availability	Price
S161106-5g	5g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$70.90
S161106-25g	25g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$210.90
S161106-100g	100g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$759.90
S161106-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$3,416.90

View related series

HCA1 receptor Agonist

Basic Description

Synonyms	D-Lactic acid\|10326-41-7\|(R)-Lactic acid\|(R)-2-Hydroxypropanoic acid\|D-(-)-Lactic acid\|(2R)-2-hydroxypropanoic acid\|(-)-Lactic acid\|Propanoic acid, 2-hydroxy-, (2R)-\|D-lactate\|(R)-(-)-Lactic acid\|(R)-2-Hydroxypropionic acid\|(R)-lactate\|D-Milchsaeure\|D-2-H
Specifications & Purity	Moligand™, ≥90%(T)
Biochemical and Physiological Mechanisms	In animals, lactic acid is a metabolic compound produced by proliferating cells and during anaerobic conditions such as strenuous exercise. Lactic acid can be oxidized back to pyruvate or converted to glucose via gluconeogenesis. Lactic acid is preferenti
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads
Grade	Moligand™
Action Type	AGONIST
Mechanism of action	Agonist of HCA 1 receptor
Product Description	Lactic acid is used as a reagent in organic synthesis (in the manufacture of adhesives). It is used in the leather, textile, and tanning industries. It may be used as a plasticizer, a catalyst, or an acidifying agent. Lactic acid has even been used as a flavoring agent in the manufacture of tobacco products.

Associated Targets

FTO Tchem Alpha-ketoglutarate-dependent dioxygenase FTO 0 Activities

Discover Target: FTO

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLCO2A1 Tchem Solute carrier organic anion transporter family member 2A1 0 Activities

Discover Target: SLCO2A1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLCO2B1 Tchem Solute carrier organic anion transporter family member 2B1 0 Activities

Discover Target: SLCO2B1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC16A10 Tbio Monocarboxylate transporter 10 0 Activities

Discover Target: SLC16A10

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

HCAR1 Tchem Hydroxycarboxylic acid receptor 1 1 Activities

Discover Target: HCAR1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC16A7 Tchem Monocarboxylate transporter 2 0 Activities

Discover Target: SLC16A7

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC16A3 Tchem Monocarboxylate transporter 4 0 Activities

Discover Target: SLC16A3

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC16A1 Tchem Monocarboxylate transporter 1 0 Activities

Discover Target: SLC16A1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

IUPAC Name

(2R)-2-hydroxypropanoic acid

INCHI

InChI=1S/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)/t2-/m1/s1

InChi Key

JVTAAEKCZFNVCJ-UWTATZPHSA-N

Canonical SMILES

CC(C(=O)O)O

Isomeric SMILES

C[C@H](C(=O)O)O

PubChem CID

61503

Molecular Weight

90.08

Reaxy-Rn

1720252

PubChem CID

DrugBank Ligand

ChEBI

CAS Registry No.

ChEMBL Ligand

RCSB PDB Ligand

GPCRdb Ligand

Certificates

Certificate of Analysis(COA)

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10 results found

Lot Number	Certificate Type	Date	Item
F2404014	Certificate of Analysis	Jul 05, 2023	S161106
G2326283	Certificate of Analysis	Jul 05, 2023	S161106
G2326562	Certificate of Analysis	Jul 05, 2023	S161106
G2326585	Certificate of Analysis	Jul 05, 2023	S161106
G2326589	Certificate of Analysis	Jul 05, 2023	S161106
G2326594	Certificate of Analysis	Jul 05, 2023	S161106
F2307328	Certificate of Analysis	Jun 24, 2022	S161106
G2213380	Certificate of Analysis	Jun 24, 2022	S161106
G2213382	Certificate of Analysis	Jun 24, 2022	S161106
G2213383	Certificate of Analysis	Jun 24, 2022	S161106

Solubility

Soluble in water (50mg/ml)

Sensitivity

heat sensitive

Refractive Index

1.43

Specific Rotation[α]

13° (C=2.5,1.5mol/L NaOH)

Flash Point(°C)

110 °C

Safety and Hazards(GHS)

Pictogram(s)	GHS05, GHS07
Signal	Danger
Hazard Statements	H315:Causes skin irritation H318:Causes serious eye damage
Precautionary Statements	P280:Wear protective gloves/protective clothing/eye protection/face protection. P302+P352:IF ON SKIN: wash with plenty of water. P321:Specific treatment (see ... on this label). P264:Wash hands [and …] thoroughly after handling. P362+P364:Take off contaminated clothing and wash it before reuse. P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes. P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing. P317:Get emergency medical help. P332+P317:If skin irritation occurs: Get medical help.
Reaxy-Rn	1720252
Merck Index	5335

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