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Cat. No. | Product Name | ||
---|---|---|---|
L5800 | 药物代谢杂质库 | 197 compounds | |
197 种药物异构体/代谢产物的特有集合,可用于高通量、高内涵筛选; |
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T7058 |
Selisistat S-enantiomer
EX-527 S-enantiomer,(1S)-6-氯-2,3,4,9-四氢-1H-咔唑-1-甲酰胺,EX-527 (S-enantiomer) |
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Selisistat S-enantiomer (EX-527 S-enantiomer) 是一种选择性的SIRT1抑制剂,IC50值为 98 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。 | |||
T6156 |
Ruxolitinib (S enantiomer)
S-Ruxolitinib,环丙基[4-[3-(1H-咪唑-5-基)丙氧基]苯,Ruxolitinib S enantiomer,INCB018424,INCB18424 |
Tyrosine Kinases; JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors |
Ruxolitinib S enantiomer (INCB18424) 是 Ruxolitinib 的 S 型对映体,是一种JAK 抑制剂。 | |||
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。 | |||
T9825 |
CORT-108297 Enantiomer
|
Others | Others |
CORT-108297 Enantiomer 是 CORT-108297 的对映体,CORT-108297是糖皮质激素受体的拮抗剂。 | |||
T7695 |
PNU-282987 S enantiomer free base
|
AChR | Neuroscience |
PNU-282987 S enantiomer free base 是 PNU-282987 的 S 型对映体,是 α7 烟碱乙酰胆碱受体的激动剂。 | |||
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。 | |||
T10819 |
Cipropride S enantiomer
|
Others | Others |
Cipropride S enantiomer 是止吐药环普必利的S 对映体。 | |||
T19112L |
Sacubitril Enantiomer
2R,4S-Sacubitril,LCZ 696杂质A,ahu377 isomer 2 |
Others | Others |
Sacubitril Enantiomer (ahu377 isomer 2) 是 Sacubitril 的对映体,它是一种脑啡肽酶抑制剂。 | |||
T80678 |
(S)-AK-242
(-)-Resatorvid,(S)-Resatorvid,AK-242 (S enantiomer),(-)-AK-242 |
Others | Others |
(S)-AK-242 ((S)-Resatorvid) 是一种细胞因子抑制剂,可用于治疗心脏病、自身免疫性疾病、炎症性疾病。 | |||
T22450 |
Tyrphostin B44, (+) enantiomer
酪氨酸磷酸化抑制剂AG 835 |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Tyrphostin B44, (+) enantiomer 是一种表皮生长因子受体 (EGFR) 激酶抑制剂,IC50 为 0.86 μM,活性低于 (-) 对映体。 | |||
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. | |||
T12200 |
Firsocostat S enantiomer
ND-630 S enantiomer,NDI-010976 S enantiomer,GS-0976 S enantiomer |
Others | Others |
Firsocostat S enantiomer is the less active S enantiomer of Firsocostat. | |||
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。 | |||
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. | |||
T11391 |
Gepotidacin S enantiomer
GSK2140944 S enantiomer |
Others | Others |
Gepotidacin S enantiomer is an S enantionmer of gepotidacin. | |||
T11173 |
Elacestrant S enantiomer
RAD1901 S enantiomer |
Others | 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 | 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. | |||
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. | |||
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). | |||
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). | |||
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. | |||
T13120 |
Tenalisib R Enantiomer
RP6530 R Enantiomer |
Others | Others |
Tenalisib R Enantiomer is an R enantiomer of Tenalisib . | |||
T11156 |
Nazartinib S-enantiomer
EGF816 (S-enantiomer) |
Others | 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 | Cell Cycle/Checkpoint |
Atuveciclib S-Enantiomer (BAY-1143572 S-Enantiomer) 是 BAY-1143572的 S-对映异构体 ,是一种有效的选择性 CDK9抑制剂,抑制 CDK9/CycT1,IC50为 16 nM。 | |||
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. | |||
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. | |||
T11173L |
Elacestrant S enantiomer dihydrochloride
RAD1901 S enantiomer dihydrochloride,RAD-1901 S enantiomer dihydrochloride,RAD 1901 S enantiomer dihydrochloride |
Others | 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 low activity enantiomer of elacestrant dihydrochloride. | |||
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). | |||
T10252L |
ADU-S100 enantiomer ammonium salt
MIW815 enantiomer ammonium salt,ML RR-S2 CDA enantiomer ammonium salt |
Others | 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). | |||
T67880 |
NITD-609 Enantiomer
|
Others | Others |
NITD-609 Enantiomer 是 NITD-609 的对映体,NITD-609 是一种具有抗疟活性的螺酮类药物。 | |||
T11628 |
IACS-8968 S-enantiomer
IDO/TDO Inhibitor (S-enantiomer) |
IDO | Metabolism |
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). | |||
T9848 |
GSK2850163 (S enantiomer)
|
IRE1 | Cell Cycle/Checkpoint |
GSK2850163 (S enantiomer) 是 GSK2850163 的无活性对映体。GSK2850163 是一种新型的肌醇需求酶-1α (IRE1a) 抑制剂。 | |||
T39541 |
THK5351 (R enantiomer)
|
Others | Others |
THK5351 R enantiomer is an R enantiomer of THK5351. | |||
T41114 |
LIN28 inhibitor LI71 enantiomer
|
Others | Others |
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, effectively blocking LIN28-mediated oligouridylation with an IC50 of 7 uM. | |||
T22401 |
PNU-282987 S enantiomer hydrochloride
(S)-PNU-282987 HCl |
Others | Others |
(S)-PNU-282987 is the absolute stereochemistry form of PNU-282987. PNU 282987, a potent agonist of α7-containing neuronal nicotinic acetylcholine receptors (nAChRs) with Ki of 26 nM for the rat receptor, has negligible activity against α1β1γδ and α3β4 nAC | |||
T12915 |
Silvestrol aglycone (enantiomer)
|
Others | Others |
Silvestrol aglycone (enantiomer) is a cyclopenta benzofuran core phenol. | |||
T11195 |
Enantiomer of Sofosbuvir
|
Others | Others |
Enantiomer of Sofosbuvir 是Sofosbuvir 的对映异构体,Sofosbuvir 是一种治疗慢性丙型肝炎的处方药,目前尚无enantiomer of Sofosbuvir 的生物活性报道。 | |||
T12067 |
MK-7246 S enantiomer
|
Others | Others |
MK-7246 S enantiomer is a potent and selective CRTH2 antagonist. | |||
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. | |||
T12203 |
Necrostatin 2 S enantiomer
|
Others | Others |
Necrostatin 2 S enantiomer is the S enantiomer of Necrostatin 2 | |||
T11902 |
LY 344864 S-enantiomer
|
Others | Others |
LY 344864 S-enantiomer, the S-enantiomer of LY344864, serves as a 5-HT1F receptor agonist. | |||
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。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5113 |
L-GLUCOSE
L-葡萄糖,L-(-)-Glucose |
Others | Others |
L-Glucose (L-(-)-Glucose) 是一种 D-glucose 的对映体,可促进食物的摄取。 | |||
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。 | |||
T5218 |
DL-Threitol
|
Others | Others |
DL-Threitol 是苏糖醇的 D-对映异构体。它具有作为人体代谢物的作用。它是 L-苏糖醇的对映异构体。 | |||
T20191 |
(-)-Camphoric acid
(-)-樟脑酸,L-Camphoric acid,Camphoric acid, (-)- |
GluR | Neuroscience |
(-)-Camphoric acid (L-Camphoric acid) 是一种活性较低的樟脑酸对映异构体,樟脑酸可诱导 GluR 表达。 | |||
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。 | |||
T1317 |
Cinchonidine
奎宁树,α-Quinidine,辛可尼丁,L-Cinchonidine |
5-HT Receptor; Serotonin Transporter; Parasite | GPCR/G Protein; Microbiology/Virology; Neuroscience |
Cinchonidine (L-Cinchonidine) 是在金鸡纳和角蒿中发现的一种生物碱,有抗疟活性。 它是用于有机化学中不对称合成的砌块,是血清素转运蛋白的弱抑制剂。 | |||
T12796 |
S-Dihydrodaidzein
S-二氢大豆苷元,(3S)-7-hydroxy-3-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one |
Others | Others |
S-Dihydrodaidzein ((3S)-7-hydroxy-3-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one) 是一种 dihydrodaidzein 的 (S) 型对映体。其中 dihydrodaidzein 是一种可食用性植物雌激素。 | |||
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。 | |||
T38251 |
L-Uridine
|
Nucleoside Antimetabolite/Analog; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
L-Uridine 是从Polyporaceae fungus Poria cocos (Schw.)分离得到的正常 RNA 成分中的 D-尿苷的对映异构体,属于一种核苷,可充当核苷磷酸转移酶的磷酸受体。L-Uridine 具有潜在的抗病毒活性。 | |||
TN1448 |
(-)-Bornyl acetate
L-(-)-Bornyl acetate,左旋乙酸冰片酯,Bornyl acetate,(-)-乙酸龙脑酯 |
p38 MAPK; NF-κB; JNK; Antifungal | MAPK; Microbiology/Virology; NF-κB |
(-)-Bornyl acetate (L-(-)-Bornyl acetate) 是存在于牛膝草油中的一种具有抗真菌活性的 (+)-Bornyl acetate 低活性异构体。 | |||
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。 | |||
TQ0109 |
Cephaeline dihydrochloride
(-)-Cephaeline dihydrochloride,盐酸吐根酚碱,NSC 32944 |
P450 | Metabolism |
(-)-Cephaeline (dihydrochloride) is an enantiomer of Cephaeline. Cephaeline is a selective CYP2D6 inhibitor (IC50: 121 μM). | |||
T13464L |
(-)-Ketoconazole
(-)-R 41400,(-)-Ketoconazol |
Others | Others |
(-)-Ketoconazole is one of the enantiomer of Ketoconazole. Ketoconazole is a racemic mixture of two enantiomers. | |||
TN7293 |
(+)-Secoisolariciresinol
|
Others | Others |
(+)-Secoisolariciresinol,是Secoisolariciresinol的一种(+)-对映体,归属于木脂素化合物。 | |||
T40529 |
(R)-(-)-1,2-Propanediol
|
Others | Others |
(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. | |||
TN7546 |
(+)-Oxanthromicin
|
Others | Others |
(+)-Oxanthromicin, an enantiomer of the rare Streptomyces metabolite (−)-oxanthromicin, demonstrates inhibitory activity against K-Ras plasma membrane localization in MDCK cells, exhibiting an IC50 value of 62.5 μM. | |||
T72509 |
Apoptosis inducer 5
|
Others | Others |
Apoptosisinducer 5 是一种木脂素对映异构体,存在于Crataegus pinnatifida 中。Apoptosisinducer 5 通过 Hep3B 细胞中的凋亡和自噬表现出细胞毒性作用。 | |||
TN7543 |
(S)-Laudanosine
NSC 35045,L-(+)-Laudanosine,(+)-Laudanosine,L-Laudanosine |
Others | Others |
(S)-Laudanosine, the (S) enantiomer of laudanosine, emerges as a metabolite from the neuromuscular blocking agents atracurium and cisatracurium. It functions by inhibiting prolyl endopeptidase and obstructing arachidonic acid- and collagen-induced aggregation in washed rabbit platelets. | |||
T40576 |
(S)-Salsolidine
|
Others | Others |
(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. | |||
TN7296 |
(+)-Butin
|
Others | Others |
(+)-Butin为Butin的R型对映体,主要从黄檀心材中分离得到,是一种具有显著抗氧化、抗血小板及抗炎活性的生物活性黄酮类化合物。 | |||
T38497 |
(-)-Taxifolin
(-)-二氢槲皮素,(-)-Dihydroquercetin |
Others | Others |
(-)-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 antifibrotic potential, while also acting as a capable free radical scavenger and possessing antioxidant capacity. | |||
T83138 |
Aloinoside A
|
||
Aloinoside A,一种可自黄芪分离的芦荟素,为Aloinoside B的对映异构体,应用于代谢研究的生物标志物。其通过大鼠肠道细菌代谢生成物包括芦荟苷、异芦荟苷及羟基代谢物。 | |||
TN4469 |
Lyoniresinol
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Lyoniresinol 是一种从 Tarenna attenuata 分离出来的木质素,具有清除自由基的活性(IC50为82.4μM)和 DPPH 的抗氧化活性,显示出抗黑色素生成活性。Lyoniresinol 有强烈的苦味,而其对映体(-)-Lyoniresinol 是无味的。 |
Cat. No. | Product Name | Species | Expression System |
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TMPH-00178 |
AiiA Protein, Bacillus thuringiensis subsp., Recombinant (His & Myc)
N-acyl homoserine lactonase AiiA,AHL-lactonase AiiA |
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. AiiA Protein, Bacillus thuringiensis subsp., Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 35.7 kDa and the accession number is P0CJ63. |
Cat. No. | Product Name | Target | Signaling Pathways |
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T27210 |
DRX-065
DRX 065,DRX065,deuterated R-enantiomer of pioglitazone |
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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 | |||
TMIJ-0155 |
rac-Aprepitant-d4 (enantiomer)
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rac-Aprepitant-d4 (enantiomer) 是 rac-Aprepitant 的氘代化合物。rac-Aprepitant 的 CAS 号为 170729-80-3。 | |||
TMIJ-0098 |
threo-Hydrobupropion-d9 HCl(enantiomer)
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threo-Hydrobupropion-d9 HCl(enantiomer) 是 threo-Hydrobupropion HCl 的氘代化合物。 | |||
TMIJ-0169 |
erythro-Hydro Bupropion-d9 HCl(enantiomer)
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erythro-Hydro Bupropion-d9 HCl(enantiomer) 是 erythro-Hydro Bupropion HCl 的氘代化合物。 | |||
TMIJ-0188 |
(±)-Voriconazole-d3 (Mixture of Enantiomers)
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(±)-Voriconazole-d3 (Mixture of Enantiomers) 是 (±)-Voriconazole 的氘代化合物。(±)-Voriconazole 的 CAS 号为 188416-29-7。 | |||
T12638 |
(R)-Praziquantel-d11
(R)-吡喹酮 D11,(R)-Praziquantel D11 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
(R)-Praziquantel D11 is the deuterium labeled (R)-Praziquantel. (R)-Praziquantel is the active enantiomer of Praziquantel, is a partial the human 5-HT2B receptor agonist | |||
T12656 |
(Rac)-Apremilast D5
(Rac)-CC-10004 D5 |
Others | Others |
(Rac)-Apremilast D5 is a deuterium-labeled version of the enantiomer (R)-Apremilast, also known as (R)-CC-10004, which itself is one specific form of Apremilast. | |||
T12648 |
(R)-VX-984
(R)-M9831 |
Others | Others |
(R)-VX-984 ((R)-M9831) is the (R)-enantiomer of VX-984. VX-984 is a potent inhibitor of DNA-PK. | |||
T12800 |
(S)-(+)-Ibuprofen D3
(S)-Ibuprofen D3 |
COX | Immunology/Inflammation; Neuroscience |
(S)-(+)-Ibuprofen D3 is a deuterium labeled (S)-(+)-Ibuprofen. (S)-(+)-Ibuprofen is the S(+)-enantiomer of Ibuprofen ,it is an inhibitor of COX-1 and COX-2 activity (IC50s of 2.1 μM and 1.6 μM). | |||
TMIJ-0231 |
Hydroxy Pentoxifylline-d6
rac-Lisofylline-d6 |
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Hydroxy Pentoxifylline-d6 是 Hydroxy Pentoxifylline 的氘代化合物。Hydroxy Pentoxifylline 的 CAS 号为 6493-06-7。(±)-Lisofylline 是一种对映异构体特异性、烷基取代的甲基黄嘌呤,在下调白细胞活化方面具有特异性和有效的活性。它是一种抗炎剂。 | |||
TMID-0190 |
Milnacipran-d10 Hydrochloride
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Milnacipran-d10 Hydrochloride 是 Milnacipran Hydrochloride 的氘代化合物。Milnacipran Hydrochloride 的 CAS 号为 101152-94-7。Milnacipran hydrochloride 是一种5-羟色胺-去甲肾上腺素重吸收抑制剂(SNRI),可用于纤维肌痛的研究。 | |||
TMIJ-0141 |
(S)-Amlodipine-d4
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(S)-Amlodipine-d4 是 (S)-Amlodipine 的氘代化合物。(S)-Amlodipine 的 CAS 号为 103129-82-4。Levamlodipine 是一种二氢吡啶钙通道阻滞剂,具有舒张血管的作用,可用于高血压和心绞痛的研究。 | |||
TMIH-0159 |
Citalopram-d6
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Citalopram-d6 是 Citalopram 的氘代化合物。Citalopram 的 CAS 号为 59729-33-8。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。 |