MedKoo Cat#: 574084 | Name: HTMT dimaleate
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

HTMT is a histamine H1 receptor agonist that binds to the histamine H4 receptor but does not increase calcium mobilization. HTMT increases intracellular calcium and inositol phosphate levels as well as proliferation of cholangiocytes.

Chemical Structure

HTMT dimaleate
HTMT dimaleate
CAS#195867-54-0(maleate)

Theoretical Analysis

MedKoo Cat#: 574084

Name: HTMT dimaleate

CAS#: 195867-54-0(maleate)

Chemical Formula: C23H29F3N4O5

Exact Mass: 498.2090

Molecular Weight: 498.50

Elemental Analysis: C, 55.42; H, 5.86; F, 11.43; N, 11.24; O, 16.05

Price and Availability

Size Price Availability Quantity
5mg USD 350.00 2 Weeks
10mg USD 600.00 2 Weeks
25mg USD 950.00 2 Weeks
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Related CAS #
No Data
Synonym
Histamine trifluromethyl toluidine, HTMT
IUPAC/Chemical Name
6-((2-(1H-imidazol-5-yl)ethyl)amino)-N-(4-(trifluoromethyl)phenyl)heptanamide dimaleate
InChi Key
ODAOZWTYNWZSBY-SPIKMXEPSA-N
InChi Code
InChI=1S/C19H25F3N4O.2C4H4O4/c1-14(24-11-10-17-12-23-13-25-17)4-2-3-5-18(27)26-16-8-6-15(7-9-16)19(20,21)22;2*5-3(6)1-2-4(7)8/h6-9,12-14,24H,2-5,10-11H2,1H3,(H,23,25)(H,26,27);2*1-2H,(H,5,6)(H,7,8)/b;2*2-1-
SMILES Code
CC(NCCC1=CN=CN1)CCCCC(NC2=CC=C(C(F)(F)F)C=C2)=O.O=C(O)/C=C\C(O)=O.O=C(O)/C=C\C(O)=O
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 498.50 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1. Shayo, C., Fernandez, N., Legnazzi, B.L., et al. Histamine H2 receptor desensitization: Involvement of a select array of G protein-coupled receptor kinases. Mol. Pharmacol. 60(5), 1049-1056 (2001). 2. Zhu, Y., Michalovich, D., Wu, H., et al. Cloning, expression, and pharmacological characterization of a novel human histamine receptor. Mol. Pharmacol. 59(3), 434-441 (2001). 3. Qiu, R., Melmon, K.L., and Kahn, M.M. Effects of histamine-trifluoromethyl-toluidide derivative (HTMT) on intracellular calcium in human lymphocytes. J. Pharmacol. Exp. Ther. 253(3), 1245-1252 (1990). 4. Francis, H., Glaser, S., Demorrow, S., et al. Small mouse cholangiocytes proliferate in response to H1 histamine receptor stimulation by activation of the IP3/CaMK I/CREB pathway. Am. J. Physiol. Cell Physiol. 295(2), C499-C513 (2008). 5. Tripathi, T., Shahid, M., Khan, H.M., et al. Modulation of in vivo immunoglobulin production by endogenous histamine and H1R and H2R agonists and antagonists. Pharmacol. Rep. 62(5), 917-925 (2010). 6. Bell, J.K., McQueen, D.S., and Rees, J.L. Involvement of histamine H4 and H1 receptors in scratching induced by histamine receptor agonists in BalbC mice. Br. J. Pharmacol. 142(2), 374-380 (2004).