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108

抑制剂 & 化合物

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Cat. No.	Product Name	Target	Signaling Pathways
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。
T10819	Cipropride S enantiomer	Others	Others
	Cipropride S enantiomer 是止吐药环普必利的S 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。
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。
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。
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。
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.
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.
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.
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
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。
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.
T10757	Cenobamate S-Enantiomer	Others	Others
	Cenobamate S-Enantiomer is a Cenobamate's S-enantiomer.
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.
T12067	MK-7246 S enantiomer	Others	Others
	MK-7246 S enantiomer is a potent and selective CRTH2 antagonist.
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).
T12203	Necrostatin 2 S enantiomer	Others	Others
	Necrostatin 2 S enantiomer is the S enantiomer of Necrostatin 2
T11378	GDC-0834 S-enantiomer	Others	Others
	GDC-0834, the S-enantiomer, is a potent and selective inhibitor of Bruton's tyrosine kinase (BTK).
T11902	LY 344864 S-enantiomer	Others	Others
	LY 344864 S-enantiomer, the S-enantiomer of LY344864, serves as a 5-HT1F receptor agonist.
T10517	BET-BAY 002 (S enantiomer)	Others	Others
	BET-BAY 002 S enantiomer为BET-BAY 002的S型对映异构体，属于BET小分子抑制剂。
T13294	Veledimex (S enantiomer) RG-115932 S enantiome,INXN-1001 S enantiome	Others	Others
	Veledimex S enantiomer is the S enantiomer of veledimex. Veledimex is an oral activator ligand for a proprietary gene therapy promoter system and CYP3A4/5 inhibitor.
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。
T10297	AMG 487 (S-enantiomer)	Others	Others
	AMG 487 S-enantiomer is the S enantiomer of AMG 487. AMG 487 is an CXCR3 antagonist.
T0448	(S)-(+)-Ibuprofen 左旋布洛芬,Dexibuprofen,(S)-Ibuprofen,(S)-(+)-布洛芬	BCL; Thrombin; Cysteine Protease; COX; PPAR	Apoptosis; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Neuroscience; Proteases/Proteasome
	(S)-(+)-Ibuprofen (Dexibuprofen) 是 Ibuprofen 的 S(+)-对映异构体，能够有效的抑制COX-1(IC50:2.1 μM)和COX-2(IC50:1.6 μM)，。它具有抗癌、退热、止痛，抗炎的效果。
T6493	Escitalopram Oxalate 草酸右旋西酞普兰,依他普仑草酸盐,Cipralex,(S)-(+)Citalopram oxalate	Others; 5-HT Receptor; Serotonin Transporter	GPCR/G Protein; Neuroscience; Others
	Escitalopram Oxalate ((S)-(+)Citalopram oxalate) 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。
T75251	Firsocostat (S enantiomer)
	Firsocostat S enantiomer (ND-630 S enantiomer) 是 Firsocostat 的低活性的 S 型异构体。Firsocostat 是乙酰辅酶 A 羧化酶抑制剂。
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.
T13869	Ribocil B Ribocil S enantiomer,ent-Ribocil A	Others	Others
	Ribocil-B is the active S-isomer of ribocil which can inhibit flavin mononucleotide (FMN,KD of 6.6 nM).
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).
T12814	(S)-Tenofovir (S)-替诺福韦,(S)-PMPA,(S)-GS 1278,(S)-TDF	Others	Others
	(S)-Tenofovir ((S)-PMPA) 是Tenofovir 的活性较低的S-对映体，Tenofovir 是一种核苷酸逆转录酶抑制剂。
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。
T39979	(S)-ErSO	Others	Others
	(S)-ErSO 是 ErSO 的无活性右旋对映异构体。
T12809	(S)-PF-06873600	CDK	Cell Cycle/Checkpoint
	(S)-PF-06873600 是 CDK 抑制剂 PF-06873600 的 S 对映体。
T22359	MDL 100009	5-HT Receptor	GPCR/G Protein; Neuroscience
	MDL 100009 是 MDL 100151 的 S-对映体和 MDL 100907 的相反对映体，是 5-HT2A 的选择性拮抗剂。
T1211	Levosulpiride RV-12309,左旋舒必利,左舒必利,S-(-)-Sulpiride	Dopamine Receptor	GPCR/G Protein; Neuroscience
	Levosulpiride (S-(-)-Sulpiride) 是 Sulpiride 的(S)对映体，是一种多巴胺 D2受体拮抗剂。
T6566	Levobupivacaine hydrochloride Levobupivacaine HCl,(S)-(-)-Bupivacaine HCl,盐酸左布比卡因,(S)-(-)-Bupivacaine monohydrochloride	Sodium Channel	Membrane transporter/Ion channel
	Levobupivacaine hydrochloride ((S)-(-)-Bupivacaine monohydrochloride) 是有效的钠通道阻滞剂。
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。
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。
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。
T6038	(-)-Blebbistatin (S)-(-)-Blebbistatin	ATPase; Myosin	Cytoskeletal Signaling; Membrane transporter/Ion channel
	(-)-Blebbistatin ((S)-(-)-Blebbistatin) 是 blebbistatin 的 S 对映异构体。它是一种有效的选择性肌球蛋白 II 抑制剂，IC50 范围为 0.5 至 5 μM。
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。
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.
T6357	(S)-crizotinib ent-crizotinib	Apoptosis; DNA/RNA Synthesis; MTH1	Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	(S)-crizotinib (ent-crizotinib) 是一种选择性MTH1(mutT 同源物)抑制剂，IC50为 330 nM。它通过抑制 MTH1 破坏核苷酸库的稳态，诱导 DNA 单链断裂的增加，激活人结肠癌细胞的 DNA 修复，在动物模型中抑制肿瘤生长。
T9828	N-[1-(Aminocarbonyl)-4-[(2-chloro-1-iminoethyl)amino]butyl]benzamide	PAD	Chromatin/Epigenetic
	N-[1-(Aminocarbonyl)-4-[(2-chloro-1-iminoethyl)amino]butyl]benzamide 是Cl-amidine (S 构型)的消旋形式。Cl-amidine 口服有效的 PAD 抑制剂。
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)。
T1545	Levamlodipine 左旋氨氯地平,(S)-Amlodipine,S-amlodipine	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Levamlodipine (S-amlodipine) 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。
T4284	Levamlodipine besylate 左旋氨氯地平,(S)-Amlodipine Besylate (103129-82-4(free base))	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Levamlodipine besylate ((S)-Amlodipine Besylate(103129-82-4(free base))) 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。
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。
T1787	Levobupivacaine	Sodium Channel	Membrane transporter/Ion channel
	Levobupivacaine 是一种氨基酰胺类局麻药，属于n-alkylsubstituted pipecoloxylidide 家族。它是bupivacaine 的 S-对映异构体。

化合物

PNU-282987 S enantiomer free base

Cat.No: T7695

Target: AChR

Cipropride S enantiomer

Cat.No: T10819

Target: Others

Selisistat S-enantiomer

Cat.No: T7058

Synonym: EX-527 S-enantiomer,(1S)-6-氯-2,3,4,9-四氢-1H-咔唑-1-甲酰胺,EX-527 (S-enantiomer)

Target: Sirtuin

Tipifarnib (S enantiomer)

Cat.No: T17102

Synonym: Tipifarnib S enantiomer,(S)-(-)-R-115777,(S)-Tipifarnib,IND-58359 S enantiomer

Target: Transferase

Cat.No: T80678

Synonym: (-)-Resatorvid,(S)-Resatorvid,AK-242 (S enantiomer),(-)-AK-242

Target: Others

Ruxolitinib (S enantiomer)

Cat.No: T6156

Synonym: S-Ruxolitinib,环丙基[4-[3-(1H-咪唑-5-基)丙氧基]苯,Ruxolitinib S enantiomer,INCB018424,INCB18424

Target: Tyrosine Kinases, JAK

Fulvestrant (S enantiomer)

Cat.No: T11335

Synonym: ZM 182780 S enantiomer,ICI 182780 S enantiomer,Fulvestrant S enantiomer,ZD 9238 S enantiomer

Target: Others

Firsocostat S enantiomer

Cat.No: T12200

Synonym: ND-630 S enantiomer,NDI-010976 S enantiomer,GS-0976 S enantiomer

Target: Others

Gepotidacin S enantiomer

Cat.No: T11391

Synonym: GSK2140944 S enantiomer

Target: Others

Elacestrant S enantiomer

Cat.No: T11173

Synonym: RAD1901 S enantiomer

Target: Others

PNU-282987 S enantiomer hydrochloride

Cat.No: T22401

Synonym: (S)-PNU-282987 HCl

Target: Others

Atuveciclib S-Enantiomer

Cat.No: T10465

Synonym: BAY-1143572 S-Enantiomer

Target: CDK

Nazartinib S-enantiomer

Cat.No: T11156

Synonym: EGF816 (S-enantiomer)

Target: Others

Cenobamate S-Enantiomer

Cat.No: T10757

Target: Others

Elacestrant S enantiomer dihydrochloride

Cat.No: T11173L

Synonym: RAD1901 S enantiomer dihydrochloride,RAD-1901 S enantiomer dihydrochloride,RAD 1901 S enantiomer dihydrochloride

Target: Others

MK-7246 S enantiomer

Cat.No: T12067

Target: Others

IACS-8968 S-enantiomer

Cat.No: T11628

Synonym: IDO/TDO Inhibitor (S-enantiomer)

Target: IDO

Necrostatin 2 S enantiomer

Cat.No: T12203

Target: Others

GDC-0834 S-enantiomer

Cat.No: T11378

Target: Others

LY 344864 S-enantiomer

Cat.No: T11902

Target: Others

BET-BAY 002 (S enantiomer)

Cat.No: T10517

Target: Others

Veledimex (S enantiomer)

Cat.No: T13294

Synonym: RG-115932 S enantiome,INXN-1001 S enantiome

Target: Others

GSK2850163 (S enantiomer)

Cat.No: T9848

Target: IRE1

AMG 487 (S-enantiomer)

Cat.No: T10297

Target: Others

(S)-(+)-Ibuprofen

Cat.No: T0448

Synonym: 左旋布洛芬,Dexibuprofen,(S)-Ibuprofen,(S)-(+)-布洛芬

Target: BCL, Thrombin, Cysteine Protease, COX, PPAR

Escitalopram Oxalate

Cat.No: T6493

Synonym: 草酸右旋西酞普兰,依他普仑草酸盐,Cipralex,(S)-(+)Citalopram oxalate

Target: Others, 5-HT Receptor, Serotonin Transporter

Firsocostat (S enantiomer)

Cat.No: T75251

INT-777 R-enantiomer

Cat.No: T11662

Synonym: S-EMCA R enantiomer

Target: Others

Cat.No: T13869

Synonym: Ribocil S enantiomer,ent-Ribocil A

Target: Others

ADU-S100 enantiomer ammonium salt

Cat.No: T10252L

Synonym: MIW815 enantiomer ammonium salt,ML RR-S2 CDA enantiomer ammonium salt

Target: Others

Cat.No: T12814

Synonym: (S)-替诺福韦,(S)-PMPA,(S)-GS 1278,(S)-TDF

Target: Others

(S)-Mirtazapine

Cat.No: T12632L

Synonym: (S)-6-Azamianserin,(S)-Org3770

Target: 5-HT Receptor

Cat.No: T39979

Target: Others

(S)-PF-06873600

Cat.No: T12809

Target: CDK

Cat.No: T22359

Target: 5-HT Receptor

Cat.No: T1211

Synonym: RV-12309,左旋舒必利,左舒必利,S-(-)-Sulpiride

Target: Dopamine Receptor

Levobupivacaine hydrochloride

Cat.No: T6566

Synonym: Levobupivacaine HCl,(S)-(-)-Bupivacaine HCl,盐酸左布比卡因,(S)-(-)-Bupivacaine monohydrochloride

Target: Sodium Channel

α1 adrenoceptor-MO-1

Cat.No: T10003

Target: Others

Cat.No: T10012

Target: Others

(S)-Lisofylline

Cat.No: T22148

Target: Others

(-)-Blebbistatin

Cat.No: T6038

Synonym: (S)-(-)-Blebbistatin

Target: ATPase, Myosin

Cat.No: T4295

Synonym: GNE-140

Target: Dehydrogenase

Levocetirizine Dihydrochloride

Cat.No: T22354

Synonym: Xyzal Dihydrochloride,(-)-Cetirizine Dihydrochloride

Target: Histamine Receptor

Cat.No: T6357

Synonym: ent-crizotinib

Target: Apoptosis, DNA/RNA Synthesis, MTH1

N-[1-(Aminocarbonyl)-4-[(2-chloro-1-iminoethyl)amino]butyl]benzamide

Cat.No: T9828

Target: PAD

(S)-(+)-Rolipram

Cat.No: T6649

Synonym: (S)-Rolipram,(+)-Rolipram,盐酸环胞苷,S- (+)-Rolipram

Target: Apoptosis, PDE

Cat.No: T1545

Synonym: 左旋氨氯地平,(S)-Amlodipine,S-amlodipine

Target: Calcium Channel

Levamlodipine besylate

Cat.No: T4284

Synonym: 左旋氨氯地平,(S)-Amlodipine Besylate (103129-82-4(free base))

Target: Calcium Channel

Cat.No: T20828

Synonym: Cipram,Lu 10-171,Lu-10-171 Lu10-171

Target: 5-HT Receptor

Levobupivacaine

Cat.No: T1787

Target: Sodium Channel

Cat. No.	Product Name	Target	Signaling Pathways
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。
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。
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。
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.

天然产物

Cat.No: T0185

Synonym: Seroplex,依他普仑,S-(+)-Citalopram,艾司西酞普兰,(S)-Citalopram

Target: Dopamine Receptor, 5-HT Receptor, Serotonin Transporter, Adrenergic Receptor, AChR, Norepinephrine, Histamine Receptor

S-Dihydrodaidzein

Cat.No: T12796

Synonym: S-二氢大豆苷元,(3S)-7-hydroxy-3-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one

Target: Others

Cat.No: T4000

Synonym: Equol,(±)-雌马酚,(R,S)-Equol

Target: Estrogen Receptor/ERR, Estrogen/progestogen Receptor, Drug Metabolite

Cat.No: T6491

Synonym: (−)-Equol,Equol,4',7-Dihydroxyisoflavan,4',7-Isoflavandiol,雌马酚

Target: Estrogen Receptor/ERR, Estrogen/progestogen Receptor, Endogenous Metabolite

(S)-Salsolidine

Cat.No: T40576

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