125
6
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12064 |
Niraparib (R-enantiomer)
MK 4827 (R-enantiomer),Niraparib R-enantiomer |
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Niraparib R-enantiomer (MK 4827 R-enantiomer) 是一种 PARP1抑制剂,IC50为 2.4 nM。 | |||
T12831 |
SAR405 R enantiomer
|
Others | Others |
SAR405 R enantiomer 是一种 PIK3C3/Vps34 抑制剂,也是活性低于 SAR405 的对映体。 | |||
T15263 |
Selisistat R-enantiomer
EX-527 (R-enantiomer) |
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Selisistat R-enantiomer (EX-527 (R-enantiomer)) 是 Selisistat R 型对映体。Selisistat 是SIRT1的选择性抑制剂,IC50为98 nM。 | |||
T12697 |
Refametinib R enantiomer
RDEA119 R enantiomer,Refametinib R enantiomer,BAY 869766 R enantiomer |
MEK | MAPK |
Refametinib R enantiomer (RDEA119 R enantiomer) 是一种 MEK 抑制剂,EC50为 2.0-15 nM。Refametinib R enantiomer 具有抗癌活性,可用于研究癌症。 | |||
T13140 |
Umbralisib R-enantiomer
TGR-1202 R-enantiomer,RP5264 R-enantiomer |
PI3K | PI3K/Akt/mTOR signaling |
Umbralisib R-enantiomer (RP5264 R-enantiomer) 是 PI3K 的δ型抑制剂,是 TGR-1202 活性较低的对映体。Umbralisib R-enantiomer 对δ型 pi3激酶的 IC50,至少比抑制剂对其他 PI3K 亚型(A, β和γ)的 IC50低20倍。 | |||
T19618 |
(R)-(-)-JQ1 Enantiomer
(R)-(-)2-(4-(4-氯苯基)-2,3,9-三甲基-6H-噻吩并[3,2-F][1,2,4]三唑并[4,3-A][1,4]二氮杂环庚烷-6-基)乙酸叔丁酯 |
Epigenetic Reader Domain | Chromatin/Epigenetic |
(R)-(-)-JQ1 Enantiomer 是 (+)-JQ1 的立体异构体。 (+)-JQ1 是一种 BET 溴结构域抑制剂,对BRD4(1/2)的IC50 为 77 和 33 nM。 | |||
T11129L |
Duvelisib (R enantiomer) hydrochloride
IPI-145 R enantiomer HCl,Duvelisib (R enantiomer) hydrochloride(1261590-48-0 Free base),INK1197 R enantiomer HCl |
PI3K | PI3K/Akt/mTOR signaling |
Duvelisib (R enantiomer) hydrochloride (INK1197 R enantiomer HCl) 是 PI3K 抑制剂。Duvelisib (R enantiomer) hydrochloride 是 Duvelisib 的活性较低的对映体。 | |||
T39541 |
THK5351 (R enantiomer)
|
||
THK5351 R enantiomer is an R enantiomer of THK5351. | |||
T17102 |
Tipifarnib (S enantiomer)
Tipifarnib S enantiomer,(S)-(-)-R-115777,(S)-Tipifarnib,IND-58359 S enantiomer |
Transferase | Metabolism |
Tipifarnib S enantiomer ((S)-(-)-R-115777) 是Tipifarnib 的 S 型对映体,它比 Tipifarnib 特性低。其中 Tipifarnib 是farnesyltransferase 高效特异性抑制剂,IC50=0.6 nM。 | |||
T12274 |
Siremadlin (R Enantiomer)
Siremadlin R Enantiomer,HDM201 R Enantiomer,NVP-HDM201 R Enantiomer |
Others | Others |
Siremadlin R Enantiomer is the R enantiomer of Siremadlin. Siremadlin is a potent and highly specific inhibitor of MDM-2/p53. | |||
T11334 |
Fulvestrant (R enantiomer)
ICI 182780 R enantiomer,ZD 9238 R enantiomer,ZM 182780 R enantiomer,Fulvestrant R enantiomer |
Others | 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. | |||
T13120 |
Tenalisib R Enantiomer
RP6530 R Enantiomer |
Others | Others |
Tenalisib R Enantiomer is an R enantiomer of Tenalisib . | |||
T11129 |
Duvelisib (R enantiomer)
Duvelisib R enantiomer,IPI-145 R enantiomer,INK1197 R enantiomer |
PI3K | PI3K/Akt/mTOR signaling |
Duvelisib R enantiomer (IPI-145 R enantiomer) 是一种 Duvelisib 的对映异构体,活性较低。 它是一种 PI3K 抑制剂。 | |||
T13422L |
Talarozole (R enantiomer)
(R)-Talarozole,Talarozole R enantiomer |
Others | Others |
Talarozole R enantiomer is a potent and selective inhibitor of cytochrome P450 26-mediated breakdown of endogenous all-trans retinoic acid. | |||
T10552 |
Bitopertin (R enantiomer)
RO4917838 (R enantiomer),RG1678 (R enantiomer),Bitopertin R enantiomer |
GlyT | Neuroscience |
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). | |||
T11410 |
GLPG0492 (R enantiomer)
GLPG0492 R enantiomer |
Others | 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 | Others |
RSV604 R enantiomer is the R-enantiomer of RSV604. RSV604 is a respiratory syncytial virus (RSV) replication inhibitor. | |||
T67881 |
Acalabrutinib enantiomer
R-Acalabrutinib |
BTK | Angiogenesis; Tyrosine Kinase/Adaptors |
Acalabrutinib enantiomer (R-Acalabrutinib) 是一类属于布鲁顿酪氨酸激酶(BTK)抑制剂的化合物。Acalabrutinib enantiomer 可用于癌症、自身免疫性疾病和慢性炎症等领域的研究。 | |||
T10856 |
Cobimetinib (R-enantiomer)
考比替尼 (R 型对映体),XL-518 R-enantiomer,Cobimetinib R-enantiomer,GDC-0973 R-enantiomer |
Others | Others |
Cobimetinib R-enantiomer is the less active R-enantiomer of Cobimetinib which is a selective MEK inhibitor. | |||
T13312 |
Seviteronel R enantiomer
VT-464 (R enantiomer) |
Others | Others |
Seviteronel R enantiomer is the R enantiomer of Seviteronel and is a potent inhibitor of CYP17 lyase (IC50: 69 nM for h-Lyase). | |||
T12723 | Ribocil-C R enantiomer | Others | Others |
Ribocil-C R enantiomer is the R enantiomer of Ribocil-C. Ribocil-C is a highly selective bacterial riboflavin riboswitches inhibitor. | |||
T11841 |
Leu-AMS R enantiomer
|
Others | Others |
Leu-AMS R enantiomer 是 Leu-AMS 的 R 对映体。 Leu-AMS 是一种有效的亮氨酰-tRNA 合成酶 (LRS) 抑制剂,可抑制细菌的生长。 | |||
T11662 |
INT-777 R-enantiomer
S-EMCA R enantiomer |
Others | Others |
INT-777 is the R-enantiomer of INT-777, less potent than INT-777,EC50 of 4.79 μM for TGR5. | |||
T11627 |
IACS-8968 R-enantiomer
IDO/TDO Inhibitor (R-enantiomer) |
IDO | Metabolism |
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). | |||
T12096 |
Morinidazole (R enantiomer)
R-Morinidazole,R-吗啉硝唑 |
Others | Others |
Morinidazole (R enantiomer) is the R-enantiomer of Morinidazole. | |||
T12612 |
(R)-Apremilast
R-阿普斯特,(R)-CC-10004 |
Others | Others |
(R)-Apremilast ((R)-CC-10004) 是一种 Apremilast 的异构体。 | |||
T20898 |
(R)-Propranolol hydrochloride
Dexpropranolol hydrochloride,(R)-(+)-Propranolol,盐酸普奈洛尔 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
(R)-Propranolol hydrochloride (Dexpropranolol hydrochloride) 是一种抗肾上腺素受体拮抗剂,是一种普萘洛尔的活性较低的对映体。Dexpropranolol 是一种非选择性的β-adrenergic receptor 拮抗剂,对 β1AR 和 β2AR 具有高亲和力。 | |||
T10608 |
BRD5648
(R)-BRD0705 |
GSK-3 | PI3K/Akt/mTOR signaling; Stem Cells |
BRD5648 ((R)-BRD0705) 是 BRD0705 的 阴性对照,BRD0705 是旁系选择性和口服有效的 GSK3α 抑制剂,Kd 为 4.8 μM,IC50为 66 nM。与 GSK3β (IC50为 515 nM) 相比,BRD0705 对 GSK3α 的选择性更高 (8 倍)。BRD0705 可用于急性髓细胞性白血病。 | |||
T27210 |
DRX-065
DRX 065,DRX065,deuterated R-enantiomer of pioglitazone |
||
DRX-065 is a stabilized and deuterated R-enantiomer of pioglitazone. DRX-065 has pharmacological properties desirable for the treatment of NASH (mitochondrial function modulation, non-steroidal anti-inflammatory effects, and glucose lowering effects) with | |||
T13448 |
(R)-(-)-Rolipram
(R)-Rolipram,(-)-Rolipram |
DNA-PK; Others | DNA Damage/DNA Repair; Others; PI3K/Akt/mTOR signaling |
(R)-(-)-Rolipram ((-)-Rolipram) 是一种 PDE4 抑制剂 Rolipram 的 R-对映异构体。 | |||
T12624 |
(R)-Ketorolac
(+)-Ketorolac,(1R)-5-苯基-2,3-二氢-1H-吡啶-1-羧酸 |
Others | Others |
(R)-Ketorolac ((+)-Ketorolac) 是一种 Ketorolac 的 R 型对应体,对 COX 无作用,具有镇痛作用,并可以减少溃疡的发生。 | |||
T36839 |
(R)-Mephenytoin
R-Mephenytoin,(R)-Mephenytoin,(–)-Mephenytoin |
Others | Others |
(R)-Mephenytoin ((–)-Mephenytoin) 是 Mephenytoin 的 R-对映体,Mephenytoin 是一种抗惊厥药。 | |||
T70388L |
(R)-Enitociclib
|
CDK | Cell Cycle/Checkpoint |
(R)-Enitociclib 是 BAY-1251152的一个对映体,是 CDK9 抑制剂,具有抗癌活性。 | |||
T17309 |
(R)-(-)-Ibuprofen
levibuprofen,(R)-Ibuprofen |
NF-κB | NF-κB |
(R)-(-)-Ibuprofen ((R)-Ibuprofen) 是 Ibuprofen 的 R 型异构体,对 COX 无作用,可以抑制 NF-κB 的活化;(R)-(-)-Ibuprofen 具有抗炎作用,可用于缓解疼痛的研究。 | |||
T5843 |
Tarenflurbil
MPC7869,(R)-Flurbiprofen,R-flurbiprofen,氟比洛芬,R-氟比洛芬 |
Retinoid Receptor; Autophagy | Autophagy; Metabolism |
Tarenflurbil ((R)-Flurbiprofen) 是 Flurbiprofen 的 R 型对映体,可抑制 [3H]9-cis-RA 结合到 RXRαLBD,IC50为 75 μM。它可研究阿尔兹海默症。 | |||
T10012 |
P7C3-OMe
|
Others | Others |
P7C3-OMe 是促神经原性化合物,其 R-对映体活性远高于 S-对映体。可以用于研究神经精神疾病和神经退行性疾病。 | |||
T12632L |
(S)-Mirtazapine
(S)-6-Azamianserin,(S)-Org3770 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
(S)-Mirtazapine ((S)-Org3770) 是 Mirtazapine 的 S(+)-对映体。(S)-Mirtazapine 是一种选择性 5-HT2 受体拮抗剂,具有促痛觉作用,常与Mirtazapine 的 R(-)-对映体混合使用来研究抑郁症。 | |||
T10003 |
α1 adrenoceptor-MO-1
|
Others | Others |
α1 adrenoceptor-MO-1(S 对映体)对α1肾上腺素受体具有亲和力,具有抗α-肾上腺素能和镇痛作用。α1 adrenoceptor-MO-1比R 对映体更具活性。 | |||
T12632 |
(R)-Mirtazapine
(R)-Org3770,(R)-6-Azamianserin |
5-HT Receptor | GPCR/G Protein; Neuroscience |
(R)-Mirtazapine ((R)-Org3770) 是 Mirtazapine 的 R(-)-对映体,在急性热痛觉动物模型中具有抗伤害感受的特性。(R)-Mirtazapine 是 5-HT3 受体的拮抗剂,是一种潜在的镇痛剂。 | |||
T22148 |
(S)-Lisofylline
|
Others | Others |
(S)-Lisofylline 是抗炎剂 (R)-lisofylline 的非活性光学对映异构体。 (S)-Lisofylline 在人肝微粒体中专门转化为己酮可可碱。 | |||
T10174 |
5-R-Rivaroxaban
|
Factor Xa | Metabolism |
5-R-Rivaroxaban 是一种 Rivaroxaban 的 R 型对映体。其中 Rivaroxaban 是选择性的Factor Xa(FXa) 抑制剂。 | |||
T12628 |
(R)-MG-132
(S,R,S)-(-)-MG-132,N-[(苯基甲氧基)羰基]-L-亮氨酰-N-[(1S)-1-甲酰基-3-甲基丁基]-D-亮氨酰胺,Z-Leu-D-leu-leu-al |
Proteasome | Proteases/Proteasome; Ubiquitination |
(R)-MG-132 (Z-Leu-D-leu-leu-al) 是一种 MG-132 的对映异构体,是一种蛋白酶体 (proteasome) 抑制剂,细胞毒性比 MG-132 弱,是一种比 MG-132 更有效的proteasome 抑制剂。 | |||
T4295 |
(R)-GNE-140
GNE-140 |
Dehydrogenase | Metabolism |
(R)-GNE-140 (GNE-140) 是 LDHA 抑制剂,能够作用于 LDHA (IC50:3 nM) 和 LDHB (IC50:3 nM)。它的活性是 S 型异构体的 18 倍。 | |||
T12643 |
(R)-Terazosin
(R)-特拉唑嗪,盐酸特拉唑嗪 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
(R)-Terazosin 是一种 Terazosin 的活性 R 型对映体, 是 α1-肾上腺素受体拮抗剂,对 α1a,α1b 和α1d-肾上腺素受体的Ki 分别为 6.51 nM,1.01 nM 和 1.97 nM。 | |||
T13428 |
(5R)-BW-4030W92
|
Sodium Channel | Membrane transporter/Ion channel |
(5R)-BW-4030W92是 R 型的 BW-4030W92 ,是具有活性的对映体。(5R)-BW-4030W92 是一种可口服的非选择性、电压依赖性和使用依赖性的钠离子通道 (sodium channel) 拮抗剂,可用于研究神经系统疾病。 | |||
T22354 |
Levocetirizine Dihydrochloride
Xyzal Dihydrochloride,(-)-Cetirizine Dihydrochloride |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Levocetirizine Dihydrochloride (Xyzal Dihydrochloride) is a third-generation peripheral H1-receptor antagonist. Acting as an antihistaminic agent, it specifically targets the histamine H1-receptor. Levocetirizine Dihydrochloride is the R-enantiomer of Cetirizine, which gives it a higher affinity for the H1-receptor than the S-enantiomer. Due to this enhanced affinity, Levocetirizine Dihydrochloride is effective in treating allergic rhinitis and chronic idiopathic urticaria. | |||
T6396 |
(R)-(-)-Gossypol acetic acid
(-)-Gossypol acetic acid,AT-101 (acetic acid),(R)-Gossypol acetic acid,AT101醋酸,AT101,AT101 acetate |
BCL; Autophagy | Apoptosis; Autophagy |
(R)-(-)-Gossypol acetic acid (AT101 acetate) 是天然产物 Gossypol 的左旋异构体,与 Bcl-2、Bcl-xL 和 Mcl-1 结合,Ki 为 0.32 μM、0.48 μM 和 0.18 μM。 | |||
T10776 |
CFTR corrector 4
|
CFTR | Membrane transporter/Ion channel |
CFTR corrector 4是一种高效且可口服的囊性纤维化跨膜电导调节剂 (CFTR),是一种有效的 (R,R) 型活性对映体。CFTR corrector 4 可以增加细胞表面的 CFTR 水平,是用来研究囊性纤维化的潜在化合物。 | |||
T6649 |
(S)-(+)-Rolipram
(S)-Rolipram,(+)-Rolipram,盐酸环胞苷,S- (+)-Rolipram |
Apoptosis; PDE | Apoptosis; Metabolism |
(S)-(+)-Rolipram ((+)-Rolipram) 是一种 cAMP 依赖性磷酸二酯酶 4 (PDE4) 抑制剂,IC50=1100 nM。它能够抑制人单核细胞产生的肿瘤坏死因子 α (TNFα)。 | |||
T20828 |
Citalopram
Cipram,Lu 10-171,Lu-10-171 Lu10-171 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Citalopram (Lu 10-171) 是一种具有口服活性的、选择性的血清素再摄取抑制剂 (SSRI),是一种选择性5-羟色胺再摄取抑制剂,是一种 S(+)-对映体 (Escitalopram) 和 R(-)-对映体的外消旋混合物。Citalopram 具有抗抑郁活性,可增强血清素能神经传递,可用于研究老年痴呆。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10935 |
D-Glutamic acid
(R)-Glutamic acid,D-谷氨酸 |
Endogenous Metabolite | Metabolism |
D-Glutamic acid ((R)-Glutamic acid) 是一种广泛用于药物和食品中的L-glutamic acid 对映异构体。 | |||
T4000 |
(±)-Equol
Equol,(±)-雌马酚,(R,S)-Equol |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Drug Metabolite | Endocrinology/Hormones; Metabolism |
(±)-Equol ((R,S)-Equol) 是 equol 的外消旋体。它对 ERα 和 ERβ 的 EC50s of 分别为 200 和 74 nM。Equol 是大豆异黄酮黄豆苷和大豆黄素的代谢产物。 | |||
T6491 |
(-)-(S)-Equol
(−)-Equol,Equol,4',7-Dihydroxyisoflavan,4',7-Isoflavandiol,雌马酚 |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
(-)-(S)-Equol (4',7-Dihydroxyisoflavan) 是雌激素受体β的高亲和力配体。 | |||
T0185 |
Escitalopram
Seroplex,依他普仑,S-(+)-Citalopram,艾司西酞普兰,(S)-Citalopram |
Dopamine Receptor; 5-HT Receptor; Serotonin Transporter; Adrenergic Receptor; AChR; Norepinephrine; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Escitalopram (Seroplex) 是一种外消旋 Citalopram 的 S-对映体,是一种选择性 5-羟色胺再摄取抑制剂,Ki=0.89 nM,比 R(-)-enantiomer 结合亲和力高 30 倍。它对多巴胺转运体和去甲肾上腺素转运体均有选择性,是一种研究抑郁症的抗抑郁药。 | |||
T40529 |
(R)-(-)-1,2-Propanediol
|
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(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. | |||
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, boasting a K i value of 26 μM compared to the S form. |