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カタログ番号 | 製品名 | 別名 | ターゲット |
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T12697 | Refametinib R enantiomer | RDEA119 R enantiomer,Refametinib R enantiomer,BAY 869766 R enantiomer | MEK |
T12064 | Niraparib (R-enantiomer) | MK 4827 (R-enantiomer),Niraparib R-enantiomer | PARP |
Niraparib R-enantiomer (MK 4827 R-enantiomer) is an inhibitor of PARP1(IC50 of 2.4 nM). | |||
T7058 | Selisistat S-enantiomer | EX-527 S-enantiomer,EX-527 (S-enantiomer) | Sirtuin |
Selisistat S-enantiomer (EX-527 S-enantiomer) is an effective and specific SIRT1 inhibitor (IC50 = 98 nM) and shows >200-fold selectivity against SIRT2/3. | |||
T13140 | Umbralisib R-enantiomer | TGR-1202 R-enantiomer,RP5264 R-enantiomer | PI3K |
Umbralisib R-enantiomer (RP5264 R-enantiomer) is a delta inhibitor of PI3K and a less active enantiomer of TGR-1202. The IC50 of Umbralisib R-enantiomers against δPI3 kinase is at least 20 times lower than that of the in... | |||
T15263 | Selisistat R-enantiomer | EX-527 (R-enantiomer) | Sirtuin |
Selisistat R-enantiomer (EX-527 (R-enantiomer)) is a SIRT1 inhibitor with much less activity than the R-enantiomer of Selisistat (IC50 of SIRT1 > 100 μM). | |||
T11129L | Duvelisib (R enantiomer) hydrochloride | IPI-145 R enantiomer HCl,Duvelisib (R enantiomer) hydrochloride(1261590-48-0 Free base),INK1197 R enantiomer HCl | PI3K |
Duvelisib (R enantiomer) hydrochloride (INK1197 R enantiomer HCl) is a PI3K inhibitor. Duvelisib (R enantiomer) hydrochloride is the less active enantiomer of Duvelisib. | |||
T6156 | Ruxolitinib (S enantiomer) | S-Ruxolitinib,Ruxolitinib S enantiomer,INCB018424,INCB18424 | Tyrosine Kinases , JAK |
Ruxolitinib S enantiomer (INCB18424) is the S-enantiomer of Ruxolitinib. Ruxolitinib is the first potent, selective JAK1/2 inhibitor. | |||
T17102 | Tipifarnib (S enantiomer) | Tipifarnib S enantiomer,(S)-(-)-R-115777,(S)-Tipifarnib,IND-58359 S enantiomer | Transferase |
Tipifarnib S enantiomer ((S)-(-)-R-115777) is the S-enantiomer of Tipifarnib. Tipifarnib is a potent and specific farnesyltransferase inhibitor (IC50: 0.6 nM). | |||
T12831 | SAR405 R enantiomer | Others | |
SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is an inhibitor of PIK3C3/Vps34. | |||
T19618 | (R)-(-)-JQ1 Enantiomer | Epigenetic Reader Domain | |
(R)-(-)-JQ1 Enantiomer is the stereoisomer of (+)-JQ1. (+)-JQ1 is a BET bromodomain inhibitor, acting on BRD4(1/2)(IC50 of 77 nM/33 nM in a cell-free assay) | |||
T19112L | Sacubitril Enantiomer | 2R,4S-Sacubitril,ahu377 isomer 2 | Others |
Sacubitril Enantiomer (ahu377 isomer 2) is the enantiomer of Sacubitril which is a neprilysin inhibitor. | |||
T9825 | CORT-108297 Enantiomer | Others | |
CORT-108297 Enantiomer is an enantiomer of CORT-108297 which is an antagonist of the Glucocorticoid Receptor. | |||
T10819 | Cipropride S enantiomer | Others | |
Cipropride S enantiomer is the S enantiomer of cipropride which is an antiemetic drug. | |||
T7695 | PNU-282987 S enantiomer free base | AChR | |
PNU-282987 S enantiomer free base is an agonist of α7 nicotinic acetylcholine receptor (α7 nAChR). | |||
T67881 | Acalabrutinib enantiomer | R-Acalabrutinib | BTK |
Acalabrutinib enantiomer (R-Acalabrutinib) is a chemical compound that belongs to the class of Bruton’s tyrosine kinase (BTK) inhibitors. Acarabitinib enantiomers can be used in the study of cancer, autoimmune diseases a... | |||
T22450 | Tyrphostin B44, (+) enantiomer | EGFR | |
Tyrphostin B44, (+) enantiomer is an inhibitor of epidermal growth factor receptor (EGFR) kinase with IC50 of 0.86 μM and has less active than the (-) enantiomer. | |||
T80678 | (S)-AK-242 | (-)-Resatorvid,(S)-Resatorvid,AK-242 (S enantiomer),(-)-AK-242 | Others |
(S)-AK-242 ((S)-Resatorvid) is a cytokine inhibitor used in the treatment of heart disease, autoimmune disease, and inflammatory disease. | |||
T10552 | Bitopertin (R enantiomer) | RO4917838 (R enantiomer),RG1678 (R enantiomer),Bitopertin R enantiomer | GlyT |
Bitopertin R enantiomer (RG1678 R enantiomer) is the R-enantiomer of Bitopertin. Bitopertin is a noncompetitive glycine reuptake inhibitor and inhibits glycine uptake at human GlyT1 (IC50: 25 nM). | |||
T11391 | Gepotidacin S enantiomer | GSK2140944 S enantiomer | Others |
Gepotidacin S enantiomer is an S enantionmer of gepotidacin. | |||
T11173 | Elacestrant S enantiomer | RAD1901 S enantiomer | Others |
Elacestrant S enantiomer is a selective and orally available estrogen receptor (ERR) degrader with IC50 values of 48 and 870 nM for ERα and ERβ, respectively. | |||
T11335 | Fulvestrant (S enantiomer) | ZM 182780 S enantiomer,ICI 182780 S enantiomer,Fulvestrant S enantiomer,ZD 9238 S enantiomer | Others |
Fulvestrant S enantiomer is the less active S enantiomer of Fulvestrant. Fulvestrant is a potent estrogen receptor antagonist with an IC50 of 9.4 nM. | |||
T10856 | Cobimetinib (R-enantiomer) | XL-518 R-enantiomer,Cobimetinib R-enantiomer,GDC-0973 R-enantiomer | Others |
Cobimetinib R-enantiomer is the less active R-enantiomer of Cobimetinib which is a selective MEK inhibitor. | |||
T67880 | NITD-609 Enantiomer | Others | |
NITD-609 Enantiomer is an enantiomer of NITD-609 which is a spironone drug with antimalarial activity. | |||
T13312 | Seviteronel R enantiomer | VT-464 (R enantiomer) | Others |
Seviteronel R enantiomer is the R enantiomer of Seviteronel and is a potent inhibitor of CYP17 lyase (IC50: 69 nM for h-Lyase). | |||
T11410 | GLPG0492 (R enantiomer) | GLPG0492 R enantiomer | Others |
GLPG0492 R enantiomer is the R enantiomer of GLPG-0492, a novel selective androgen receptor modulator. | |||
T12775 | RSV604 (R enantiomer) | RSV604 R enantiomer | Others |
RSV604 R enantiomer is the R-enantiomer of RSV604. RSV604 is a respiratory syncytial virus (RSV) replication inhibitor. | |||
T11156 | Nazartinib S-enantiomer | EGF816 (S-enantiomer) | Others |
Nazartinib is an EGFR inhibitor. Nazartinib S-enantiomer is the less active S-enantiomer of Nazartinib. | |||
T10465 | Atuveciclib S-Enantiomer | BAY-1143572 S-Enantiomer | CDK |
Atuveciclib S-Enantiomer (BAY-1143572 S-Enantiomer) is the (S)-enantiomer of BAY-1143572. Atuveciclib S-Enantiomer is a potent and selective CDK9 inhibitor, which inhibits CDK9 / CycT1 with an IC 50 of 16 nM. | |||
T12274 | Siremadlin (R Enantiomer) | Siremadlin R Enantiomer,HDM201 R Enantiomer,NVP-HDM201 R Enantiomer | Others |
Siremadlin R Enantiomer is the R enantiomer of Siremadlin. Siremadlin is a potent and highly specific inhibitor of MDM-2/p53. | |||
T13422L | Talarozole (R enantiomer) | (R)-Talarozole,Talarozole R enantiomer | Others |
Talarozole R enantiomer is a potent and selective inhibitor of cytochrome P450 26-mediated breakdown of endogenous all-trans retinoic acid. | |||
T11334 | Fulvestrant (R enantiomer) | ICI 182780 R enantiomer,ZD 9238 R enantiomer,ZM 182780 R enantiomer,Fulvestrant R enantiomer | Others |
Fulvestrant R enantiomer is the less active R enantiomer of Fulvestrant. Fulvestrant is a potent estrogen receptor antagonist with an IC50 of 9.4 nM. | |||
T11129 | Duvelisib (R enantiomer) | Duvelisib R enantiomer,IPI-145 R enantiomer,INK1197 R enantiomer | PI3K |
Duvelisib R enantiomer (IPI-145 R enantiomer) is an enantiomer of Duvelisib with lower activity. Duvelisib is a PI3K inhibitor. | |||
T12200 | Firsocostat S enantiomer | ND-630 S enantiomer,NDI-010976 S enantiomer,GS-0976 S enantiomer | Others |
Firsocostat S enantiomer is the less active S enantiomer of Firsocostat. | |||
T13120 | Tenalisib R Enantiomer | RP6530 R Enantiomer | Others |
Tenalisib R Enantiomer is an R enantiomer of Tenalisib . | |||
T9848 | GSK2850163 (S enantiomer) | IRE1 | |
GSK2850163 (S enantiomer) is the inactive enantiomer of GSK2850163. GSK2850163 is an novel inhibitor of inositol-requiring enzyme-1 alpha (IRE1a). | |||
T11628 | IACS-8968 S-enantiomer | IDO/TDO Inhibitor (S-enantiomer) | IDO |
IACS-8968 S-enantiomer is the S-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO). | |||
T11627 | IACS-8968 R-enantiomer | IDO/TDO Inhibitor (R-enantiomer) | IDO |
IACS-8968 R-enantiomer is the R-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO). | |||
T39541 | THK5351 (R enantiomer) | ||
THK5351 R enantiomer is an R enantiomer of THK5351. | |||
T11173L | Elacestrant S enantiomer dihydrochloride | RAD1901 S enantiomer dihydrochloride,RAD-1901 S enantiomer dihydrochloride,RAD 1901 S enantiomer dihydrochloride | Others |
Elacestrant (RAD1901) dihydrochloride is a selective and orally available estrogen receptor (ERR) degrader with IC50 values of 48 and 870 nM for ERα and ERβ, respectively. Elacestrant S enantiomer dihydrochloride is an l... | |||
T11662 | INT-777 R-enantiomer | S-EMCA R enantiomer | Others |
INT-777 is the R-enantiomer of INT-777, less potent than INT-777,EC50 of 4.79 μM for TGR5. | |||
T10252L | ADU-S100 enantiomer ammonium salt | MIW815 enantiomer ammonium salt,ML RR-S2 CDA enantiomer ammonium salt | Others |
ADU-S100 (MIW815) enantiomer ammonium salt is the less active enantiomer of ADU-S100. ADU-S100 is an activator of the stimulator of interferon genes (STING). | |||
T41114 | LIN28 inhibitor LI71 enantiomer | ||
LIN28 inhibitor LI71 enantiomer, the enantiomer of LIN28 inhibitor LI71,exhibits reduced activity compared to its parent compound. LIN28 inhibitor LI71 is a highly potent and cell-permeable inhibitor of LIN28, effectivel... | |||
T11195 | Enantiomer of Sofosbuvir | Others | |
Sofosbuvir's enantiomer, a variant of the prescription medication Sofosbuvir used for chronic hepatitis C treatment, currently lacks reported biological activity. | |||
T12915 | Silvestrol aglycone (enantiomer) | Others | |
Silvestrol aglycone (enantiomer) is a cyclopenta benzofuran core phenol. | |||
T11841 | Leu-AMS R enantiomer | Others | |
Leu-AMS R enantiomer is the R enatiomer of Leu-AMS. Leu-AMS is a potent leucyl-tRNA synthetase (LRS) inhibitor that inhibits the bacteria growth. | |||
T12203 | Necrostatin 2 S enantiomer | Others | |
Necrostatin 2 S enantiomer is the S enantiomer of Necrostatin 2 | |||
T11378 | GDC-0834 S-enantiomer | Others | |
GDC-0834, the S-enantiomer, is a potent and selective inhibitor of Bruton's tyrosine kinase (BTK). | |||
T11902 | LY 344864 S-enantiomer | Others | |
LY 344864 S-enantiomer, the S-enantiomer of LY344864, serves as a 5-HT1F receptor agonist. | |||
T12723 | Ribocil-C R enantiomer | Others | |
Ribocil-C R enantiomer is the R enantiomer of Ribocil-C. Ribocil-C is a highly selective bacterial riboflavin riboswitches inhibitor. | |||
T12067 | MK-7246 S enantiomer | Others | |
MK-7246 S enantiomer is a potent and selective CRTH2 antagonist. |
カタログ番号 | 製品名 | 別名 | ターゲット |
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T5113 | L-GLUCOSE | L-(-)-Glucose | Others |
L-Glucose (L-(-)-Glucose) is an enantiomer of D-glucose. L-Glucose is not bioavailable to cells as an energy source because it cannot be phosphorylated by hexokinase. | |||
T0185 | Escitalopram | Seroplex,S-(+)-Citalopram,(S)-Citalopram | Dopamine Receptor , 5-HT Receptor , Serotonin Transporter , Adrenergic Receptor , AChR , Norepinephrine , Histamine Receptor |
Escitalopram (Seroplex) is a furancarbonitrile that is one of the SEROTONIN UPTAKE INHIBITORS used as an antidepressant. The drug is also effective in reducing ethanol uptake in alcoholics and is used in depressed patien... | |||
T5218 | DL-Threitol | Others | |
D-threitol is the D-enantiomer of threitol. It has a role as a human metabolite. It is an enantiomer of a L-threitol. | |||
T20191 | (-)-Camphoric acid | L-Camphoric acid,Camphoric acid, (-)- | GluR |
(-)-Camphoric acid (L-Camphoric acid) is a less active enantiomer of Camphoric acid which induces GluR expression. | |||
T10935 | D-Glutamic acid | (R)-Glutamic acid | Endogenous Metabolite |
D-Glutamic acid ((R)-Glutamic acid), the enantiomer of L-glutamic acid, is widely used in medicine and food. | |||
T1317 | Cinchonidine | α-Quinidine,L-Cinchonidine | 5-HT Receptor , Serotonin Transporter , Parasite |
Cinchonidine (L-Cinchonidine) is an alkaloid extracted from Cinchona officinalis. It is a pseudo-enantiomer and stereoisomer of cinchonine. | |||
T12796 | S-Dihydrodaidzein | (3S)-7-hydroxy-3-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one | Others |
S-Dihydrodaidzein ((3S)-7-hydroxy-3-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one) is an enantiomer of dihydrodaidzein which is involved in equol biosynthesis in a lactic acid bacterium, Lactococcus sp. strain. | |||
T6396 | (R)-(-)-Gossypol acetic acid | (-)-Gossypol acetic acid,AT-101 (acetic acid),(R)-Gossypol acetic acid,AT101,AT101 acetate | BCL , Autophagy |
(R)-(-)-Gossypol acetic acid (AT101 acetate) , the R-(-) enantiomer of Gossypol acetic acid, binds with Bcl-2, Bcl-xL and Mcl-1 with Ki of 0.32 μM, 0.48 μM and 0.18 μM; does not inhibit BIR3 domain and BID. Phase 2. | |||
T38251 | L-Uridine | Nucleoside Antimetabolite/Analog , Antibiotic | |
L-Uridine is the enantiomer of D-uridine, a nucleoside that acts as a phosphate acceptor for nucleoside phosphotransferase, in the normal RNA component of a normal RNA isolated from Polyporaceae fungus Poria cocos (Schw.... | |||
TN1448 | (-)-Bornyl acetate | L-(-)-Bornyl acetate,Bornyl acetate | p38 MAPK , NF-κB , JNK , Antifungal |
(-)-Bornyl acetate (L-(-)-Bornyl acetate) is a less active enantiomer of (+)-Bornyl acetate. (-)-Bornyl acetate isolates from hyssop oil and possesses antifungal activity. (-)-Bornyl acetate shows highly active whitening... | |||
T4000 | (±)-Equol | Equol,(R,S)-Equol | Estrogen Receptor/ERR , Estrogen/progestogen Receptor , Drug Metabolite |
(±)-Equol ((R,S)-Equol) is a non-steroidal estrogen produced from the metabolism of the isoflavonoid phytoestrogen daidzen by human intestinal microflora. The estrogen receptor (ER) agonist activity of the naturally occu... | |||
T6491 | (-)-(S)-Equol | (−)-Equol,Equol,4',7-Dihydroxyisoflavan,4',7-Isoflavandiol | Estrogen Receptor/ERR , Estrogen/progestogen Receptor , Endogenous Metabolite |
(-)-(S)-Equol (4',7-Dihydroxyisoflavan) is an orally bioavailable, non-steroidal estrogen naturally produced by the metabolism of the isoflavonoid daidzein by human intestinal microflora, with potential chemoprotective a... | |||
T13464L | (-)-Ketoconazole | (-)-R 41400,(-)-Ketoconazol | Others |
(-)-Ketoconazole is one of the enantiomer of Ketoconazole. Ketoconazole is a racemic mixture of two enantiomers. | |||
TQ0109 | Cephaeline dihydrochloride | (-)-Cephaeline dihydrochloride,NSC 32944 | P450 |
(-)-Cephaeline (dihydrochloride) is an enantiomer of Cephaeline. Cephaeline is a selective CYP2D6 inhibitor (IC50: 121 μM). | |||
T40529 | (R)-(-)-1,2-Propanediol | ||
(R)-(-)-1,2-Propanediol is the (R)-enantiomer of 1,2-Propanediol, which is derived from glucose through the expression of NADH-linked glycerol dehydrogenase genes in Escherichia coli. | |||
T72509 | Apoptosis inducer 5 | ||
Apoptosis Inducer 5, a lignan enantiomer extracted from Crataegus pinnatifida, demonstrates cytotoxic properties through inducing apoptosis and autophagy in Hep3B cells. | |||
T40576 | (S)-Salsolidine | ||
(S)-Salsolidine, a chemical compound, functions as a weak inhibitor of monoamine oxidase (MAO), exhibiting an inhibition constant (K i ) of 63 μM. R enantiomer demonstrating a greater efficacy than (S)-Salsolidine, boast... | |||
T38497 | (-)-Taxifolin | (-)-Dihydroquercetin | |
(-)-Taxifolin is the less active enantiomer of Taxifolin, demonstrating vital anti-tyrosinase activity and notable inhibition against collagenase (IC50 = 193.3 μM). It is valued as an essential natural compound showing a... | |||
T83138 | Aloinoside A | ||
Aloinoside A, an aloin isolated from Astragalus membranaceus, is the enantiomer of Aloinoside B and is a biomarker used in metabolic research. Its metabolic products by rat intestinal bacteria include aloin, isoaloin and... | |||
TN4469 | Lyoniresinol | ||
Lyoniresinol is a lignan isolated from Tarenna attenuata with free radical scavenging activity (IC50 of 82.4 μM) and antioxidant activity of DPPH, showing anti-melanogenic activity. Lyoniresinol has a strong bitter taste... |
カタログ番号 | 製品名 | Species | Expression System |
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TMPH-00178 | AiiA Protein, Bacillus thuringiensis subsp., Recombinant (His & Myc) | Bacillus thuringiensis subsp. kurstaki | E. coli |
Catalyzes hydrolysis of N-hexanoyl-(S)-homoserine lactone, but not the R-enantiomer. Hydrolyzes short- and long-chain N-acyl homoserine lactones with or without 3-oxo substitution at C3, has maximum activity on C10-AHL. ... |
カタログ番号 | 製品名 | ||
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L5800 | Drug Metabolite/Impurity Library | 197 compounds | |
A unique collection of 197 drug isomers/metabolites for high throughput screening (HTS) and high content screening (HCS); |