Home > Name List By other > (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E, 3S)-3-hydroxy-3-methyloct-1-enyl]cyclopentyl]hept-5-enoic acid

CAS No 35700-23-3 , (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E,
3S)-3-hydroxy-3-methyloct-1-enyl]cyclopentyl]hept-5-enoic acid

  • Name: (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E,
    3S)-3-hydroxy-3-methyloct-1-enyl]cyclopentyl]hept-5-enoic acid
  • Synonyms: Carboprostum; 15-Methyl-pgf2-alpha (alpha and beta); Methyl-pgf2-alpha;(Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E,
    3S)-3-hydroxy-3-methyloct-1-enyl]cyclopentyl]hept-5-enoic acid; Prostin 15M; 15-Methyl prostaglandin F2alpha;35700-23-3; U 32921;
  • CAS Registry Number:
  • Density: 1.139 g/cm3
  • Water Solubility: soluble in water
  • Safety Statements: In humans very small amounts cause abortion by intramuscular, intravaginal and intraplacental routes. Experimental reproductive effects. When heated to decomposition it emits acrid smoke and fumes.
  • Molecular Weight: 368.50754
  • InchiKey: DLJKPYFALUEJCK-IIELGFQLSA-N
  • InChI: InChI=1S/C21H36O5/c1-3-4-9-13-21(2,
    26)14-12-17-16(18(22)15-19(17)23)10-7-5-6-8-11-20(24)25/h5,7,12,14,
    16-19,22-23,26H,3-4,6,8-11,13,15H2,1-2H3,(H,24,25)/b7-5-,14-12+/t16-,
    17-,18+,19-,21+/m1/s1
  • Molecular Formula: C21H36O5
  • Molecular Structure:CAS No:35700-23-3 (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E,<br />3S)-3-hydroxy-3-methyloct-1-enyl]cyclopentyl]hept-5-enoic acid

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References of (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E,
3S)-3-hydroxy-3-methyloct-1-enyl]cyclopentyl]hept-5-enoic acid
Title: Carboprost
CAS Registry Number: 35700-23-3
CAS Name: (5Z,9a,11a,13E,15S)-9,11,15-Trihydroxy-15-methylprosta-5,13-dien-1-oic acid
Synonyms: 7-[3,5-dihydroxy-2-(3-hydroxy-3-methyl-1-octenyl)cyclopentyl]-5-heptenoic acid; (15S)-15-methyl PGF2a
Manufacturers' Codes: U-32921
Molecular Formula: C21H36O5
Molecular Weight: 368.51
Percent Composition: C 68.44%, H 9.85%, O 21.71%
Literature References: Analog of prostaglandin F2a, q.v. Prepn: G. L. Bundy et al., DE 2121980; G. L. Bundy, US 3728382 (1971, 1973 both to Upjohn); eidem, Ann. N.Y. Acad. Sci. 180, 76 (1971); E. W. Yankee et al., J. Am. Chem. Soc. 96, 5865 (1974). Biological activity: J. R. Weeks et al., J. Pharmacol. Exp. Ther. 186, 67 (1973). Mechanism of action: A. I. Csapo, M. O. Pulkkinen, Prostaglandins 18, 479 (1979). Clinical studies: P. C. Schwallie, K. R. Lamborn, J. Reprod. Med. 23, 289 (1979); M. P. Mapa et al., Int. J. Gynaecol. Obstet. 20, 125 (1982). Teratological study: G. M. Szczech et al., Adv. Prostaglandin Thromboxane Res. 4, 157 (1978).
 
Derivative Type: Tromethamine salt
CAS Registry Number: 58551-69-2
Synonyms: Carboprost trometamol
Manufacturers' Codes: U-32921E
Trademarks: Hemabate (Pfizer); Prostin/15M (Pfizer)
Molecular Formula: C25H47NO8
Molecular Weight: 489.64
Percent Composition: C 61.32%, H 9.68%, N 2.86%, O 26.14%
 
Derivative Type: Methyl ester
CAS Registry Number: 35700-21-1
Synonyms: Carboprost methyl
Manufacturers' Codes: U-36384
Molecular Formula: C22H38O5
Molecular Weight: 382.53
Percent Composition: C 69.08%, H 10.01%, O 20.91%
Properties: Crystals from ether/hexane, mp 55-56°. [a]D +24° (c = 0.81 in ethanol).
Melting point: mp 55-56°
Optical Rotation: [a]D +24° (c = 0.81 in ethanol)
 
Therap-Cat: Oxytocic.
Keywords: Oxytocic; Prostaglandin/Prostaglandin Analog.