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[ CAS No. 72040-64-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 72040-64-3
Chemical Structure| 72040-64-3
Structure of 72040-64-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 72040-64-3 ]

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Product Citations

Product Details of [ 72040-64-3 ]

CAS No. :72040-64-3 MDL No. :MFCD00144853
Formula : C16H27N3O4S Boiling Point : No data available
Linear Structure Formula :- InChI Key :CMUGHZFPFWNUQT-HUBLWGQQSA-N
M.W : 357.47 Pubchem ID :446905
Synonyms :
Chemical Name :6-(5-((3aS,4S,6aR)-2-Oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)hexanoic acid

Calculated chemistry of [ 72040-64-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 24
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.81
Num. rotatable bonds : 12
Num. H-bond acceptors : 4.0
Num. H-bond donors : 4.0
Molar Refractivity : 101.18
TPSA : 132.83 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -8.02 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.96
Log Po/w (XLOGP3) : 0.65
Log Po/w (WLOGP) : 0.71
Log Po/w (MLOGP) : 1.05
Log Po/w (SILICOS-IT) : 1.78
Consensus Log Po/w : 1.23

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 1.0
Egan : 1.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -1.67
Solubility : 7.58 mg/ml ; 0.0212 mol/l
Class : Very soluble
Log S (Ali) : -3.02
Solubility : 0.345 mg/ml ; 0.000966 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.65
Solubility : 0.081 mg/ml ; 0.000226 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 4.02

Safety of [ 72040-64-3 ]

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

Application In Synthesis of [ 72040-64-3 ]

* 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 [ 72040-64-3 ]

[ 72040-64-3 ] Synthesis Path-Downstream   1~13

  • 1
  • 12-aminododecanoic acid methyl ester hydrochloride [ No CAS ]
  • [ 72040-64-3 ]
  • [ 223733-85-5 ]
  • 2
  • [ 170892-94-1 ]
  • [ 72040-64-3 ]
  • Biotinylaminocaproyl-L-methionylglycyl-L-leucyl-L-prolyl-(S-farnesyl)-L-cysteine methyl ester [ No CAS ]
  • 3
  • Glycyl-(S-palmitoyl)-L-cysteine allyl ester hydrotrifluoroacetate [ No CAS ]
  • [ 72040-64-3 ]
  • Biotinylaminocaproyl-glycyl-(S-palmitoyl)-L-cysteine allyl ester [ No CAS ]
  • 4
  • [ 72040-64-3 ]
  • Glycyl-(S-hexadecyl)-L-cysteine allyl ester hydrotrifluoroacetate [ No CAS ]
  • Biotinylaminocaproyl-glycyl-(S-hexadecyl)-L-cysteine allyl ester [ No CAS ]
  • 5
  • [ 72040-64-3 ]
  • poly(sebacic acid) [ No CAS ]
  • fluorescein-conjugated avidin [ No CAS ]
  • 6-((biotinoyl)amino)hexanoic acid-attached poly(sebacic acid) microspheres [ No CAS ]
  • 6
  • methyl 6-(+)-biotinylamidohexanoate [ No CAS ]
  • [ 72040-64-3 ]
YieldReaction ConditionsOperation in experiment
58.3% With lithium hydroxide monohydrate; In methanol;Reflux; Lithium hydroxide (4equiv) solution was added to 6 (1equiv) dissolved in methanol. The solution was heated to reflux overnight. The product 7 was precipitated as white solid. Then a hydrochloric acid solution (6 N) was added until the pH was 5. The product was filtered, and dried under vacuum.
  • 7
  • [ 4136-95-2 ]
  • [ 72040-64-3 ]
  • C23H28Cl3N3O5S [ No CAS ]
  • 8
  • [ 162827-97-6 ]
  • [ 72040-64-3 ]
  • [ 721431-24-9 ]
  • 9
  • [ 66534-97-2 ]
  • [ 72040-64-3 ]
  • 5-(2-oxohexahydrothieno[3,4-d]imidazol-6-yl)pentanoic acid {5-[bis(2-diphenylphosphanyl-ethyl)carbamoyl]pentyl}amide [ No CAS ]
  • 10
  • [ 144085-40-5 ]
  • [ 72040-64-3 ]
  • 6-[5-(2-oxohexahydrothieno[3,4-d]imidazol-4-yl)pentanoylamino]hexanoic acid {3-diphenylphosphanyl-2-[(diphenylphosphanyl)methyl]-2-methylpropyl}amide [ No CAS ]
  • 11
  • [ 72040-64-3 ]
  • [ 774183-16-3 ]
  • methyl 2-cyano-23-[6-({5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoyl}amino)hexanoyl]oxy-3,12-dioxooleana-1,9(11)-dien-28-oate [ No CAS ]
  • 12
  • [ 58-85-5 ]
  • [ 60-32-2 ]
  • [ 72040-64-3 ]
  • 13
  • [ 7689-03-4 ]
  • [ 72040-64-3 ]
  • 6-biotinylaminocaproic acid-(20s)-camptothecin [ No CAS ]
YieldReaction ConditionsOperation in experiment
39% With dmap; diisopropyl-carbodiimide; In N,N-dimethyl-formamide; at 20℃; for 48h;Inert atmosphere; General procedure: To a mixture of Biotin or 6-biotinylaminocaproic acid (0.3 mmol), camptothecin analogues (0.1 mmol) and DMF (2.5 mL) was added, 4-Dimethylaminopyridine (DMAP) (0.01 mmol) was added and N, N'-Diisopropylcarbodiimide) (DIC) (0.6 mmol) dropwise. The reaction mixture was stirred at room temperature for 2 days under N2. Solvent were removed under a reduced. The residue was purified on a silica gel chromatography (CHCl3:CH3OH = 15:1?9:1) to afford the product Biotin-(20s)-camptothecin (11). Yellow amorphous powder, yield 60percent;
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