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[ CAS No. 135-16-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 135-16-0
Chemical Structure| 135-16-0
Structure of 135-16-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 135-16-0 ]

CAS No. :135-16-0 MDL No. :MFCD00135583
Formula : C19H23N7O6 Boiling Point : -
Linear Structure Formula :- InChI Key :MSTNYGQPCMXVAQ-KIYNQFGBSA-N
M.W : 445.43 Pubchem ID :135444742
Synonyms :
L-Tetrahydrofolic acid;L-5,6,7,8-Tetrahydrofolic acid;folate-H4;th-folate;Tetrahydropteroylglutamic acid;5,6,7,8-tetrahydrofolic acid

Calculated chemistry of [ 135-16-0 ]

Physicochemical Properties

Num. heavy atoms : 32
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.32
Num. rotatable bonds : 10
Num. H-bond acceptors : 7.0
Num. H-bond donors : 8.0
Molar Refractivity : 121.03
TPSA : 211.56 Ų

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -9.46 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.27
Log Po/w (XLOGP3) : -0.63
Log Po/w (WLOGP) : -1.61
Log Po/w (MLOGP) : -0.85
Log Po/w (SILICOS-IT) : -0.61
Consensus Log Po/w : -0.69

Druglikeness

Lipinski : 2.0
Ghose : None
Veber : 1.0
Egan : 1.0
Muegge : 2.0
Bioavailability Score : 0.11

Water Solubility

Log S (ESOL) : -1.82
Solubility : 6.71 mg/ml ; 0.0151 mol/l
Class : Very soluble
Log S (Ali) : -3.34
Solubility : 0.204 mg/ml ; 0.000457 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.08
Solubility : 0.0366 mg/ml ; 0.0000822 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 4.03

Safety of [ 135-16-0 ]

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 [ 135-16-0 ]

* 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.

  • Upstream synthesis route of [ 135-16-0 ]
  • Downstream synthetic route of [ 135-16-0 ]

[ 135-16-0 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 59-30-3 ]
  • [ 135-16-0 ]
Reference: [1] Research on Chemical Intermediates, 2013, vol. 39, # 5, p. 2211 - 2218
[2] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1985, p. 1349 - 1354
[3] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1993, # 7, p. 871 - 876
[4] Journal of the Chemical Society - Series Chemical Communications, 1987, vol. No. 6, p. 470 - 472
[5] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1985, p. 1349 - 1354
  • 2
  • [ 15574-38-6 ]
  • [ 135-16-0 ]
Reference: [1] Antimicrobial Agents and Chemotherapy, 2013, vol. 57, # 10, p. 4990 - 4998
[2] International Journal of Biological Macromolecules, 2017, vol. 103, p. 1044 - 1053
  • 3
  • [ 94379-13-2 ]
  • [ 135-16-0 ]
Reference: [1] Chemical Communications, 2014, vol. 50, # 38, p. 4947 - 4950
  • 4
  • [ 4033-27-6 ]
  • [ 135-16-0 ]
Reference: [1] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1985, p. 1349 - 1354
[2] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1985, p. 1349 - 1354
[3] Antimicrobial Agents and Chemotherapy, 1995, vol. 39, # 9, p. 1920 - 1924
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