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[ CAS No. 1370261-97-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1370261-97-4
Chemical Structure| 1370261-97-4
Structure of 1370261-97-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1370261-97-4 ]

CAS No. :1370261-97-4 MDL No. :MFCD25976708
Formula : C19H24ClN9O Boiling Point : -
Linear Structure Formula :- InChI Key :RMNLLPXCNDZJMJ-IDVLALEDSA-N
M.W : 429.91 Pubchem ID :56948527
Synonyms :
P505-15 Hydrochloride;BIIB057;PRT-2607;PRT062607 Hydrochloride

Calculated chemistry of [ 1370261-97-4 ]

Physicochemical Properties

Num. heavy atoms : 30
Num. arom. heavy atoms : 17
Fraction Csp3 : 0.32
Num. rotatable bonds : 6
Num. H-bond acceptors : 6.0
Num. H-bond donors : 4.0
Molar Refractivity : 115.49
TPSA : 149.66 Ų

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -6.79 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 3.0
Log Po/w (WLOGP) : 2.19
Log Po/w (MLOGP) : 0.06
Log Po/w (SILICOS-IT) : -0.57
Consensus Log Po/w : 0.94

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 1.0
Egan : 1.0
Muegge : 0.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -4.42
Solubility : 0.0164 mg/ml ; 0.0000381 mol/l
Class : Moderately soluble
Log S (Ali) : -5.81
Solubility : 0.00067 mg/ml ; 0.00000156 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.79
Solubility : 0.00689 mg/ml ; 0.000016 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 4.21

Safety of [ 1370261-97-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1370261-97-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1370261-97-4 ]

[ 1370261-97-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1370261-97-4 ]
  • [ 320401-51-2 ]
  • C33H39N9O12 [ No CAS ]
YieldReaction ConditionsOperation in experiment
47 mg 2'-(((2S,3S,4S,5S)-3,4,5-triacetoxy-6-(methoxycarbonyl)tetrahydro-2H-pyran-2- yloxy)carbonylamino)biphenyl-2-carboxylic acid was prepared according to the procedure reported in Tetrahedron Letters (2000, vol. 41, p9173). This compound (200 mg, 0.35 mmol) was dissolved in 10 mL dry DCM and stirred at RT. To it was added BOP (146 mg, 0.385 mmol). The mixture was stirred for 45 m. To the mixture was dropwise added a slurry of 4-(3-(2H- 1,2,3- Triazol-2-yl)phenylamino)-2-((lR,2S)-2-aminocyclohexylamino)pyrimidine-5-carboxamide hydrochloride (165 mg, 0.385 mmol) and DIEA (305 mu,, 1.75 mmol) in 10 mL dry DCM. The mixture was stirred at RT for overnight to get the desired adducts as a mixture of alph and beta. The mixture was diluted with EtOAc, washed with water, dried, concentrated and subjected to flash column to isolate the adducts (47 mg, inseparable by flash column). The adduct mixture was dissolved in 15 mL methanol. To it was added 3 mL water. The mixture was stirred at RT. To it was added IN LiOH aq solution (80 mu,). The mixture was stirred for 35 m. Then another 80 of the LiOH solution was added. The reaction was quenched with IN HC1 in 20 m. The mixture was concentrated in vacuo and subjected to reverse phase preparative HPLC to isolate the title compound as the major product (17 mg), and also the minor product, (3S,4S,5R,6R)-6- ((1 S,2R)-2-(4-(3-(2H- 1 ,2,3-triazol-2-yl)phenylamino)-5-carbamoylpyrimidin-2- ylamino)cyclohexylcarbamoyloxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic acid (2 mg). MS found for C26H31N909 as (M+H)+ 614.4. UV: lambda=254 nm.
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