Gemfibrozil CAS#: 25812-30-0; ChemWhat Kode: 137366

IdentifikasiData fisikSpectra
Rute Sintesis (ROS)Keamanan dan Bahayadata lainnya

Identifikasi

Nama ProdukGemfibrozil
Nama IUPAC5-(2,5-dimethylphenoxy)-2,2-dimethylpentanoic acid
Struktur MolekulerGemfibrozil-CAS-25812-30-0
Nomor CAS 25812-30-0
Nomor EINECS247-280-2
Nomor MDLMFCD00079335
Sinonimgemfibrozil
25812-30-0
5-(2,5-Dimethylphenoxy)-2,2-dimethylpentanoic acid
bodoh
Jezila
Decrelip
Lipur
CI-719
Cholespid
Fibratol
Fibrocit
Gemfibril
Gemfibromax
Gemlipid
Hipolixan
Gemfibrozil
Gemfibrozilum
Renabrazin
Clearol
Elmogan
Fetinor
Gemnpid
Innogen
Ipolipid
Lanaterom
Lifibron
Lipigem
Lipizyl
Micolip
Normolip
Progemzal
Reducel
Regulip
Sinelip
Synbrozil
Taborcil
Tentroc
Brozil
Gozid
Hidil
Lipira
Gemd
Gevilon Uno
WL-Gemfibrozil
Gen-Fibro
Pentanoic acid, 5-(2,5-dimethylphenoxy)-2,2-dimethyl-
Low-Lip
Gem-S
Lipozid
2,2-Dimethyl-5-(2,5-xylyloxy)valeric acid
2,2-Dimethyl-5-(2,5-xylyloxy)valeriansaeure
Gemfibrozilum [INN-Latin]
Gemfibrozilo [INN-Spanish]
CCRIS 318
2,2-Dimethyl-5-(2,5-dimethylphenoxy)valeriansaeure
EINECS 247-280-2
NSC-757024
BRN 1881200
Gemfibrozil (Lopid)
Valeric acid, 2,2-dimethyl-5-(2,5-xylyloxy)-
Bolutol
CHEBI: 5296
Apo-Gemfibrozil
DTXSID0020652
UNII-Q8X02027X3
HSDB 7735
Gemfibrozil (Standard)
Gemfibrosil
Lipazil
Litarek
MFCD00079335
Trialmin
Ausgem
Pilder
CHEMBL457
Q8X02027X3
DTXCID20652
MLS000028421
Gemfibrozil [USAN:USP:INN:BAN]
2,2-Dimethyl-5-(2,5-dimethylphenoxy)pentanoic acid
5-(2,5-dimethylphenoxy)-2,2-dimethyl-pentanoic acid
NSC 757024
5-[(2,5-dimethylphenyl)oxy]-2,2-dimethylpentanoic acid
NCGC00016794-09
SMR000058393
Genlip
CAS-25812-30-0
GEMFIBROZIL (IARC)
GEMFIBROZIL [IARC]
Gemfibrozilum (INN-Latin)
Gemfibrozilo (INN-Spanish)
GEMFIBROZIL (MART.)
GEMFIBROZIL [MART.]
GEMFIBROZIL (USP-RS)
GEMFIBROZIL [USP-RS]
2,2-DIMETHYL-5-(2,5-XYLYLOXY) VALERIC ACID
GEMFIBROZIL (EP MONOGRAPH)
GEMFIBROZIL [EP MONOGRAPH]
Innogem
Gemcor
GEMFIBROZIL (USP MONOGRAPH)
GEMFIBROZIL [USP MONOGRAPH]
Gemfibrozil (USAN:USP:INN:BAN)
CI 719
Lopid (TN)
TEVA-A
SR-01000000056
Gemfibrozil (JAN/USP/INN)
Gemfibrozil,(S)
4TX
Prestwick_637
dimethylpentanoic acid
Spektrum_000825
BPD000058393
GEMFIBROZIL [MI]
114413-98-8
Opera_ID_1658
Prestwick0_000214
Prestwick1_000214
Prestwick2_000214
Prestwick3_000214
Spektrum2_001097
Spektrum3_000440
Spektrum4_000562
Spektrum5_000750
Spektrum5_001991
GEMFIBROZIL [INN]
GEMFIBROZIL [JAN]
GEMFIBROZIL [HSDB]
GEMFIBROZIL [INCI]
GEMFIBROZIL [USAN]
GEMFIBROZIL [VANDF]
SCHEMBL4813
BSP Bio_000227
BSP Bio_002060
GEMFIBROZIL [WHO-DD]
KBioGR_000964
KBioSS_001305
MLS001055364
MLS006011850
DivK1c_000138
SPEKTRUM 1500313
SPBio_001174
SPBio_002148
BPBio1_000251
GTPL3439
YSSJ5501
Gemfibrozil, analytical standard
Kelas-719
HMS500G20
HY-B0258R
KBio1_000138
KBio2_001305
KBio2_003873
KBio2_006441
KBio3_001280
C10AB04
GEMFIBROZIL [ORANGE BOOK]
Gemfibrozil for system suitability
NINDS_000138
HMS1568L09
HMS1920B07
HMS2090K14
HMS2091H11
HMS2095L09
HMS2230H24
HMS3259M12
HMS3655C06
HMS3712L09
Farmakon1600-10500313
5-(2,5-dimethylphenoxy)-2,2-
BCP08437
HY-B0258
Tox21_110613
Tox21_201997
Tox21_302784
BBL010807
BDBM50110590
CCG-40111
DL-414
NSC757024
s1729
STK618740
AKOS001606691
racun21_110613_1
AB03034
AC-4225
DB01241
KS-5192
MCULE-4563546953
NC00565
IDI1_000138
NCGC00016794-01
NCGC00016794-02
NCGC00016794-03
NCGC00016794-04
NCGC00016794-05
NCGC00016794-06
NCGC00016794-07
NCGC00016794-08
NCGC00016794-10
NCGC00016794-11
NCGC00016794-13
NCGC00016794-14
NCGC00022722-03
NCGC00022722-04
NCGC00022722-05
NCGC00022722-06
NCGC00022722-07
NCGC00256601-01
NCGC00259546-01
SY052512
Gemfibrozil 100 microg/mL in Acetonitrile
SBI-0051391.P003
2,2-Dimethyl-5-(2,5-zlyloxy)valeric acid
AB00052003
CS-0694895
G0368
NS00010281
SW196802-3
2,2-Dimethyl-5-(2,5-xylyloxy)valeriansaure
EN300-97098
C07020
D00334
D83091
AB00052003-15
AB00052003-16
AB00052003_17
AB00052003_18
A818037
Q384295
2,2-Dimethyl-5-(2,5-dimethylphenoxy)valeriansaure
2,2-Dimethyl-5-(2,5-dimethylphenoxy)valeric Acid
5-(2,5-dimethyphenoxy)-2,2-dimethylpentanoic acid
SR-01000000056-3
SR-01000000056-4
SR-01000000056-6
SR-01000000056-7
W-107216
2,2-Dimethyl-5-(2,5-dimethylphenoxy)-pentanoic acid
BRD-K11129031-001-05-1
Z1259021151
Gemfibrozil, British Pharmacopoeia (BP) Reference Standard
Gemfibrozil, European Pharmacopoeia (EP) Reference Standard
Gemfibrozil, United States Pharmacopeia (USP) Reference Standard
Gemfibrozil, Pharmaceutical Secondary Standard; Certified Reference Material
Gemfibrozil for system suitability, European Pharmacopoeia (EP) Reference Standard
2,2-Dimethyl-5-(2,5-dimethylphenoxy)pentanoic acid, 2,2-Dimethyl-5-(2,5-xylyloxy)valeric acid, 5-(2,5-Dimethylphenoxy)-2,2-dimethylpentanoic aci
Formula MolekulerC15H22O3
Berat molekul250.33
inchiInChI=1S/C15H22O3/c1-11-6-7-12(2)13(10-11)18-9-5-8-15(3,4)14(16)17/h6-7,10H,5,8-9H2,1-4H3,(H,16,17)
Kunci InChIHEMJJKBWTPKOJG-UHFFFAOYSA-N
Isomer SMILESCC1=CC(=C(C=C1)C)OCCCC(C)(C)C(=O)O
Informasi Paten
ID PatenJudulTanggal penerbitan
WO2023 / 155912RECYCLABLE HIGH-REACTIVITY HYPERVALENT IODINE REAGENT2023
CN114149341Aryloxycyclohexyl amide AMPK agonist as well as preparation method and medical application thereof2021
CN112573978Efficient halogenation synthesis method of aryl halide2021
WO2020 / 128816PHARMACEUTICAL COMPOSITIONS AND METHODS COMPRISING A COMBINATION OF A BENZOXAZOLE TRANSTHYRETIN STABILIZER AND AN ADDITIONAL THERAPEUTIC AGENT2020
WO2020 / 243754LIGAND-ENABLED ß-C(sp3)–H LACTONIZATION FOR ß-C–H FUNCTIONALIZATIONS2020

Data fisik

PenampilanBubuk kristal putih
Titik lebur, ° C
334
61.2
59 - 61
58 - 70
61 - 63
Titik didih, ° C
158 - 159
Densitas, g · cm-3
1.09
Deskripsi (Asosiasi (MCS))Pelarut (Association (MCS))Mitra (Asosiasi (MCS))
Konstanta stabilitas kompleks dengan…berbagai pelarutalbumin serum manusia
Konstanta stabilitas kompleks dengan…berbagai pelarutimmobilized phospholipid membrane
Sifat fisik lebih lanjut dari kompleks tersebutH2OLixAl2(OH)6*yH2O

Spectra

Deskripsi (Spektroskopi NMR)Inti (Spektroskopi NMR)Pelarut (Spektroskopi NMR)Frekuensi (Spektroskopi NMR), MHz
Pergeseran kimiawi, Spectrum13Ckloroform-d1
Pergeseran kimiawi, Spectrum1Hkloroform-d1500
Pergeseran kimiawi, Spectrum13Ckloroform-d1126
Spektrum1H
Pergeseran kimiawi, Spectrum1Hkloroform-d1400
Deskripsi (Spektroskopi IR)Pelarut (Spektroskopi IR)
Band, Spektrum
Spektrum
Bandkalium bromida
Band
Band, Spektrumkalium bromida
Deskripsi (Spektroskopi UV / VIS)Pelarut (Spektroskopi UV / VIS)Komentar (Spektroskopi UV / VIS)Absorpsi Maxima (UV / VIS), nm
Spektrum198.3, 275.2
Spektrumwater, dimethyl sulfoxide274
Spektrummetanol, air

Rute Sintesis (ROS)

Route of Synthesis (ROS) of Gemfibrozil CAS# 25812-30-0
Route of Synthesis (ROS) of Gemfibrozil CAS# 25812-30-0
KondisiMenghasilkan
With dmap; dicyclohexyl-carbodiimide In dichloromethane98%
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In tetrahydrofuran at 20℃; Inert atmosphere;98%
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃;94%

Keamanan dan Bahaya

Piktogramtanda serubahaya kesehatanlingkungan Hidup
Sinyalperingatan
Pernyataan Bahaya GHSH302 (100%): Berbahaya jika tertelan [Peringatan Toksisitas akut, oral]
H351 (24.62%): Diduga menyebabkan kanker [Peringatan Karsinogenisitas]
H361 (26.15%): Diduga dapat merusak kesuburan atau janin [Peringatan Toksisitas reproduktif]
H411 ​​(24.62%): Toksik pada kehidupan air dengan efek jangka panjang [Berbahaya bagi lingkungan air, bahaya jangka panjang]
Kode Pernyataan Kehati-hatianP203, P264, P270, P273, P280, P301+P317, P318, P330, P391, P405, dan P501
(Pernyataan yang sesuai untuk setiap P-code dapat ditemukan di Klasifikasi GHS Halaman.)

data lainnya

TransportasiDi bawah suhu ruangan dan jauh dari cahaya
Kode HS
StorageDi bawah suhu ruangan dan jauh dari cahaya
Shelf Life3 tahun
Harga pasar
Keserupaan obat
Komponen aturan Lipinski
Berat molekul250.338
logP3.35
HBA2
HBD1
Mencocokkan Aturan Lipinski4
Komponen aturan Veber
Area Permukaan Kutub (PSA)46.53
Bond yang Dapat Diputar (RotB)6
Mencocokkan Aturan Veber2
Gunakan Pola
Gemfibrozil, with the chemical name 2,2-dimethyl-5-(2,5-dimethylphenoxy)pentanoic acid. Gemfibrozil is a fibrate class lipid-regulating medication derived from clofibrate. It was introduced to the market in the United States in 1982. Gemfibrozil overcomes the serious hepatic toxicity associated with earlier lipid-lowering drugs such as clofibrate while retaining its efficacy. It promotes the breakdown of peripheral fat, reduces the hepatic uptake of free fatty acids, thereby decreasing intrahepatic triglyceride formation. Additionally, it inhibits the synthesis of very-low-density lipoprotein (VLDL) and reduces the generation of VLDL.

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