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79

抑制剂 & 化合物

16

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
TP2187	Ribosomal protein L3 peptide (202-222) amide	Others	Others
	Ribosomal protein L3 peptide (202-222) is a peptide with the sequenceH2N-Met-Ser-His-Arg-Lys-Tyr-Glu-Ala-Pro-Arg-His-Gly-His-Leu-Gly-Phe-Leu-Pro-Arg-Lys-Arg-amide, MW=2573.
T14391	Azidamfenicol	Antibacterial; Antibiotic	Microbiology/Virology
	Azidamfenicol 抑制核糖体肽基转移酶，Ki 为 22 µM。Azidamfenicol 是一种广谱氯霉素类抗生素。
T6877	LJH685	Apoptosis; S6 Kinase	Apoptosis; MAPK; PI3K/Akt/mTOR signaling
	LJH685 是一种选择性，ATP-竞争性的RSK 抑制剂, 抑制 RSK1/2/3 生物活性，IC50为 6、5、4 nM。
T22422	S6K-18	S6 Kinase	MAPK; PI3K/Akt/mTOR signaling
	S6K-18 是一种高度选择性的 S6K1 抑制剂，抑制 S6K1，IC50 为 52nM。
T5428	BIX 02565	LRRK2; S6 Kinase	Autophagy; MAPK; PI3K/Akt/mTOR signaling
	BIX 02565 是核糖体 S6 激酶 2 (RSK2) 抑制剂，IC50为 1.1 nM。
T2002	PF-4708671 PF4708671	S6 Kinase; Autophagy	Autophagy; MAPK; PI3K/Akt/mTOR signaling
	PF-4708671 是一种可渗透细胞的 p70 核糖体 S6 激酶抑制剂，对 S6K1的Ki 为 20 nM，IC50为 160 nM。
T4301	AD80	Raf; c-RET; Src; S6 Kinase	Angiogenesis; Apoptosis; MAPK; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	AD80 是多激酶抑制剂，可抑制 RET、RAF、SRC 和 S6K，并大大降低 mTOR 活性。
T6171	BI-D1870	S6 Kinase; Autophagy	Autophagy; MAPK; PI3K/Akt/mTOR signaling
	BI-D1870 是一种可渗透细胞和透过血脑屏障的的 ATP 竞争性核糖体 S6 激酶抑制剂，抑制 RSK1、RSK2、RSK3和 RSK4 的 IC50值分别为 31 nM、24 nM、18 nM 和15 nM。
T6878	LJI308	S6 Kinase	MAPK; PI3K/Akt/mTOR signaling
	LJI308 是泛RSK 抑制剂，对 RSK1、RSK2 和 RSK3 的IC50分别为 6、4 和 13 nM。它抑制辐照、EGF 处理和表达 KRAS 突变的细胞中 RSK (T359/S363) 和 YB-1 (S102) 的磷酸化。
T14779	BRD7389	SGK; FLT; Pim; CDK; S6 Kinase; DAPK	Angiogenesis; Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; JAK/STAT signaling; MAPK; Metabolism; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	BRD7389 是一种 RSK 家族激酶抑制剂，对 RSK1、RSK2 和 RSK3 的 IC50 分别为 1.5 μM、2.4 μM 和 1.2 μM。
T6948	Pluripotin SC1	ERK; Raf; S6 Kinase	MAPK; PI3K/Akt/mTOR signaling
	Pluripotin (SC1) 是ERK1和RasGAP 的双重抑制剂，KD 分别为 98 和 212 nM。它还抑制RSK1、RSK2、RSK3和RSK4，IC50分别为 0.5、2.5、3.3 和 10.0 μM。
T1550	Thiamphenicol 甲砜霉素,Dextrosulphenidol,Thiophenicol	Antibacterial; Antibiotic	Microbiology/Virology
	Thiamphenicol (Dextrosulphenidol) 是 Chloramphenicol 的甲基磺酰基衍生物，是一种广谱抗菌类抗生素。它与 50S 核糖体亚基结合，抑制蛋白质合成并具有抑菌作用，特别针对革兰氏阴性，革兰氏阳性需氧和厌氧菌。
T6304	AT7867	Akt; PKA; S6 Kinase	Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	AT7867 是 ATP 竞争性的Akt1/Akt2/Akt3和p70S6K/PKA 抑制剂，IC50分别为 32、17、47 和 85、20 nM。
T6159	LY-2584702 free base	S6 Kinase; mTOR	MAPK; PI3K/Akt/mTOR signaling
	LY-2584702 free base 是一种选择性的 ATP 竞争性 p70S6K 抑制剂，IC50为 4 nM，对S6K1的IC50为 2 nM，用于研究癌症治疗的试验。
T9066	Merafloxacin CI 934	SARS-CoV	Microbiology/Virology
	Merafloxacin (CI 934) 是一种氟喹诺酮类抗菌药物，也被确定为 SARS-CoV-2 的 1 PRF 抑制剂。它对革兰氏阳性菌和革兰氏阴性菌具有体外活性。
T7790	Bisindolylmaleimide V 双吲哚马来酰亚胺 V,双吲哚马来酰亚胺	PKC; S6 Kinase	Chromatin/Epigenetic; Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling
	Bisindolylmaleimide V 是一种弱蛋白激酶 C (PKC) 抑制剂( IC50 >100 µM)。
T1746	LY-2584702 tosylate salt LY2584702 tosylate	S6 Kinase	MAPK; PI3K/Akt/mTOR signaling
	LY-2584702 tosylate salt 是一种选择性的 ATP 竞争性 p70S6K 抑制剂，IC50为 4 nM，对S6K1的IC50为 2 nM，用于研究癌症治疗的试验。
T4488	GSK-25 GSK25	ROCK; S6 Kinase; mTOR	Cell Cycle/Checkpoint; Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling; Stem Cells
	GSK-25 是一种选择性的，具有口服活性的 ROCK1抑制剂。它对 31 种激酶以及 RSK1 和 p70S6K 保持良好的选择性，RSK1的 IC50 为 398 nM，p70S6K 的 IC50 为 1000nM。它可抑制 P450，对 CYP2C9、CYP2D6和 CYP3A4的 IC50分别为2.5、5.2和2.5 μM。
T2482	AT13148	ROCK; SGK; Akt; PKA; S6 Kinase	Cell Cycle/Checkpoint; Cytoskeletal Signaling; MAPK; Metabolism; PI3K/Akt/mTOR signaling; Stem Cells; Tyrosine Kinase/Adaptors
	AT13148 是一种 ATP 竞争性 AGC 激酶口服抑制剂，能够抑制 Akt1/Akt2/Akt3、p70S6K、PKA 和 ROCKI/ROCKII 的活性，IC50值分别为 38/402/50、8、3 和 6 nM/4 nM。
T3125	Amikacin sulfate Amikacin Sulfate Salt,阿米卡霉素硫酸,硫酸阿米卡星	ribosome; Antibacterial; Antibiotic	Microbiology/Virology
	Amikacin sulfate 是一种氨基糖苷类抗生素，也是卡那霉素的半合成类似物。它具有杀菌作用，直接作用于 30S 和 50S 细菌核糖体亚基，可抑制蛋白质合成。它抑制大多数革兰氏阴性细菌，还抑制易感诺卡氏菌和非结核分枝杆菌引起的感染。
T8978	DD1 3,3'-Diamino-4'-methoxyflavone,HUN85111	Proteasome	Proteases/Proteasome; Ubiquitination
	DD1 (HUN85111) 是一种蛋白酶体抑制剂，可诱导人髓系肿瘤选择性凋亡。
T6382	Amikacin disulfate 硫酸阿米卡星,Pierami,阿米卡星硫酸盐,BAY-416651 sulfate,BB-K8,Amikacin sulfate	Antibacterial; Antibiotic	Microbiology/Virology
	Amikacin disulfate (BAY-416651 sulfate) 是氨基糖苷类抗生素，也是卡那霉素的半合成类似物。它具有杀菌作用，直接作用于 30S 和 50S 细菌核糖体亚基，可抑制蛋白质合成。它对大多数革兰氏阴性细菌都有效。它还抑制易感诺卡氏菌和非结核分枝杆菌引起的感染。
T19913	CKI-7 CKI 7 2HCl,CKI-7 dihydrochloride,N-(2-氨基乙基)-5-氯异喹啉-8-磺酰胺二盐酸盐,CKI7 2HCl,CKI 7 dihydrochloride,CKI7 dihydrochloride,CKI-7 2HCl	ROCK; SGK; Casein Kinase; CDK; S6 Kinase	Cell Cycle/Checkpoint; Cytoskeletal Signaling; MAPK; Metabolism; PI3K/Akt/mTOR signaling; Stem Cells
	CKI-7 是一种有效且 ATP 竞争性的酪蛋白激酶 1 抑制剂，IC50为 6 μM，Ki 为 8.5 μM。它选择性抑制 Cdc7激酶，还抑制 SGK，S6K1以及 MSK1。
T6383	Amikacin hydrate 阿米卡星水合物,BAY416651 hydrate	Others; Antibacterial; Antibiotic	Microbiology/Virology; Others
	Amikacin hydrate (BAY416651 hydrate) 是氨基糖苷类抗生素，也是卡那霉素的半合成类似物。它具有杀菌作用，直接作用于 30S 和 50S 细菌核糖体亚基，可抑制蛋白质合成。它还抑制易感诺卡氏菌和非结核分枝杆菌引起的感染。
T6549	Isepamicin sulfate Isepamicine (Isepamycin,硫酸异帕米星,Isepamicin Sulphate,Isepacin,sch21420) Sulphate	Antibacterial; Antibiotic	Microbiology/Virology
	Isepamicin sulfate (sch21420) Sulphate) 是一种广谱氨基糖苷类抗生素，对产生 I 型 6-乙酰转移酶的菌株具有良好的活性，通过靶向细菌 30S 核糖体亚基来抑制细菌蛋白质合成。
T6448	Clindamycin hydrochloride 盐酸克林霉素,Sobelin HCl,Cleocin,Clindamycin HCl,Clinimycin HCl	Antibacterial; Antibiotic	Microbiology/Virology
	Clindamycin hydrochloride (Clinimycin HCl) 是一种半合成的林可胺类抗生素，作用于50S ribosomal 抑制蛋白质合成。
T77628	Bisindolylmaleimide III	PKC	Chromatin/Epigenetic; Cytoskeletal Signaling
	Bisindolylmaleimide III is a potent and selective inhibitor of protein kinase C (PKC).Bisindolylmaleimide III selectively interacts with PKCα or ribosomal S6 protein kinase 1 upon activation of these kinases.
T2211	Dihydrostreptomycin sulfate Dihydrostreptomycin sesquisulfate,双氢链霉索	Antibacterial; Antibiotic	Microbiology/Virology
	Dihydrostreptomycin sulfate (Dihydrostreptomycin sesquisulfate) 是一种氨基糖苷类抗生素，可研究牛、猪和羊的细菌性疾病。
T50026	Aquacycline	HSV	Microbiology/Virology
	Aquacycline 是一种广谱抗生素，通过抑制细菌中的蛋白质合成起作用。它可防止氨酰-tRNA 与复杂的 m-核糖体 RNA 结合。它还具有抗 HSV-1 活性。
T1767	BMH-21 BMH21	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	BMH-21 是一种小分子 DNA 嵌入剂，可结合核糖体 DNA 并抑制 RNA 聚合酶 I (Pol I) 转录，具有抗癌活性。
T1747	Tedizolid TR 700,特地唑胺,DA-7157,泰地唑利,Torezolid	MAO; Antibacterial; Antibiotic	Metabolism; Microbiology/Virology; Neuroscience
	Tedizolid (DA-7157)是一种新型恶唑烷酮类抗生素，可与核糖体50S 亚基的23S 核糖体 RNA 结合抑制细菌的蛋白质合成。
T3052	Sancycline Bonomycin,Norcycline,Sancyclinum,山环素,6-Demethyl-6-deoxytetracycline	Antibacterial	Microbiology/Virology
	Sancycline (Bonomycin) 是半合成四环素，通过可逆地结合 30S 核糖体亚基并通过阻断氨酰-tRNA 进入核糖体 A 位点来抑制蛋白质翻译。
T1569	Tigecycline 替加环素,GAR-936	ribosome; Antibacterial; Antibiotic; Autophagy	Autophagy; Microbiology/Virology
	Tigecycline (GAR-936) 是甘氨酰环素抗生素，对 Acinetobacter baumannii(A. baumannii) 的 MIC50和 MIC90分别为 1 和 2 mg/L。它对 E. coli(MG1655 菌株) 的平均抑制浓度 (MIC) 约 125 ng/ mL。
T16491	PF-06446846 hydrochloride	Others	Others
	PF-06446846 hydrochloride 是一种口服活性高、高选择性PCSK9(前蛋白转化酶枯草杆菌蛋白酶/kexin 9 型)翻译抑制剂。它通过在密码子34附近诱导核糖体暂停来抑制PCSK9。
T16703	Quarfloxin CX-3543	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Quarfloxin (CX-3543) 是一种氟喹诺酮衍生物，具有抗肿瘤活性，可靶向抑制RNA pol I 的活性，在神经母细胞瘤细胞中的 IC50 值在纳摩尔范围内。它破坏核糖体 DNA 模板中核仁蛋白和 G-四链体 DNA 结构之间的相互作用。
T16567	PQR530 PQR-530	PI3K; mTOR	PI3K/Akt/mTOR signaling
	PQR530 是一具有口服活性，种 ATP 竞争性的，可透过血脑屏障的 PI3K/mTORC1/2双重抑制剂，对于 PI3Kα 和 mTOR (分别为 0.84 和 0.33 nM) 的Kd 为亚摩尔。它具有抗肿瘤作用。
T36675	ERK Inhibitor
	ERK inhibitor is a cell-permeable inhibitor that binds ERK2 near its docking domain (KD = 5 μM). This prevents its interaction with protein substrates without inhibiting catalytic activity. ERK inhibitor blocks ERK-specific phosphorylation of ribosomal S6 kinase-1 and ternary complex factor Elk-1 but does not affect ERK1/2 phosphorylation by MEK1/2. Presumably through its effects on ERK, ERK inhibitor completely prevents proliferation of HeLa cells (IC50 = 15-20 μM), A549 lung carcinoma cells (I...
T22297	Clindamycin hydrochloride monohydrate Clindamycin alcoholate	Antibiotic	Microbiology/Virology
	Clindamycin hydrochloride monohydrate（Clindamycin alcoholate）是一种口服蛋白质合成抑制剂，具有在金黄色葡萄球菌中以亚抑制浓度(sub-MICs)抑制毒力因子表达的能力。其抗性来源于50S核糖体亚基（23S rRNA）的抗生素结合位点通过酶促甲基化。此外，Clindamycin hydrochloride monohydrate能显著减少杀白细胞毒素（PVL）、毒性休克-葡萄球菌毒素（TSST-1）或α-溶血素（Hla）的产生。
T10365	Arg-AMS	Others	Others
	Arg-AMS is a potent arginyl tRNA synthetase inhibitor that displays tightly bound inhibitory characteristics for the A-domains in non-ribosomal peptide synthetases (NRPS) enzymes.
T31854	Formylmethionyl-alanyl-leucine Fmet-ala-leu
	Formylmethionyl-alanyl-leucine is formed by E coli ribosomal protein L10 gene.
T25733	Lincophenicol
	Lincophenicol is an Escherichia coli ribosomal peptidyltransferase-catalyzed puromycin reaction inhibitor.
T69823	MC4
	MC4 is a first-in-class inhibitor of ribosomal RNA synthesis with antimicrobial activity against Staphylococcus aureus.
T11310	FMK-MEA	Others	Others
	FMK-MEA is a potent and selective p90 Ribosomal S6 Kinase (RSK) inhibitor.
T24819	Sparsomycin U 19183,B 120121L19,B120121L19,U-19183,U19183
	Sparsomycin is an antitumor antibiotic. It also inhibits protein synthesis in the 70S and 80S ribosomal systems.
T71199	CGP7040
	CGP7040 is a rifamycin analogue, is a protein 50S ribosomal subunit inhibitor that was being developed by Novartis.
T35769	Blasticidin A
	Blasticidin A is a bacterial metabolite originally isolated from S. resistomycificus strain 2A-327. It inhibits aflatoxin production by A. parasiticus without affecting fungal growth (IC50s = 0.25 and 1.6 μM, respectively). Blasticidin A also decreases ribosomal protein levels and inhibits protein synthesis in S. cerevisiae.
T71449	Capreomycin free base
	Capreomycin is a polypeptide antibiotic originally isolated from S. capreolus. It is active against M. tuberculosis (MIC = 10 µg/ml). Capreomycin binds to both the 30S and 50S ribosomal subunits, inhibiting protein synthesis.
T68614	Doxycycline fosfatex
	Doxycycline is a synthetic tetracycline derivative with similar antimicrobial activity. Doxycycline inhibits bacterial protein synthesis by binding to the 30S ribosomal subunit. Doxycycline has bacteriostatic activity against a broad range of Gram-positive and Gramnegative bacteria. Doxycycline has been shown to be active against most isolates of the following microorganisms, both in vitro and in clinical infections.
T31616	ELX-02 NB-124,NB 124,NB124,ELX02,ELX 02
	ELX-02, also known as NB-124, is a eukaryotic ribosomal selective glycoside (ERSG) designed to increase the read-through activity in patients with nonsense mutations and enable the production of sufficient amounts of full-length functional protein to rest
T40998	S-6123
	S-6123 is a highly effective antimicrobial compound classified under the oxazolidinone series, and it acts by selectively inhibiting ribosomal protein synthesis while not affecting DNA or RNA synthesis.

化合物

Ribosomal protein L3 peptide (202-222) amide

Cat.No: TP2187

Target: Others

Cat.No: T14391

Target: Antibacterial, Antibiotic

Cat.No: T6877

Target: Apoptosis, S6 Kinase

Cat.No: T22422

Target: S6 Kinase

Cat.No: T5428

Target: LRRK2, S6 Kinase

Cat.No: T2002

Synonym: PF4708671

Target: S6 Kinase, Autophagy

Cat.No: T4301

Target: Raf, c-RET, Src, S6 Kinase

Cat.No: T6171

Target: S6 Kinase, Autophagy

Cat.No: T6878

Target: S6 Kinase

Cat.No: T14779

Target: SGK, FLT, Pim, CDK, S6 Kinase, DAPK

Cat.No: T6948

Synonym: SC1

Target: ERK, Raf, S6 Kinase

Cat.No: T1550

Synonym: 甲砜霉素,Dextrosulphenidol,Thiophenicol

Target: Antibacterial, Antibiotic

Cat.No: T6304

Target: Akt, PKA, S6 Kinase

LY-2584702 free base

Cat.No: T6159

Target: S6 Kinase, mTOR

Cat.No: T9066

Synonym: CI 934

Target: SARS-CoV

Bisindolylmaleimide V

Cat.No: T7790

Synonym: 双吲哚马来酰亚胺 V,双吲哚马来酰亚胺

Target: PKC, S6 Kinase

LY-2584702 tosylate salt

Cat.No: T1746

Synonym: LY2584702 tosylate

Target: S6 Kinase

Cat.No: T4488

Synonym: GSK25

Target: ROCK, S6 Kinase, mTOR

Cat.No: T2482

Target: ROCK, SGK, Akt, PKA, S6 Kinase

Amikacin sulfate

Cat.No: T3125

Synonym: Amikacin Sulfate Salt,阿米卡霉素硫酸,硫酸阿米卡星

Target: ribosome, Antibacterial, Antibiotic

Cat.No: T8978

Synonym: 3,3'-Diamino-4'-methoxyflavone,HUN85111

Target: Proteasome

Amikacin disulfate

Cat.No: T6382

Synonym: 硫酸阿米卡星,Pierami,阿米卡星硫酸盐,BAY-416651 sulfate,BB-K8,Amikacin sulfate

Target: Antibacterial, Antibiotic

Cat.No: T19913

Synonym: CKI 7 2HCl,CKI-7 dihydrochloride,N-(2-氨基乙基)-5-氯异喹啉-8-磺酰胺二盐酸盐,CKI7 2HCl,CKI 7 dihydrochloride,CKI7 dihydrochloride,CKI-7 2HCl

Target: ROCK, SGK, Casein Kinase, CDK, S6 Kinase

Amikacin hydrate

Cat.No: T6383

Synonym: 阿米卡星水合物,BAY416651 hydrate

Target: Others, Antibacterial, Antibiotic

Isepamicin sulfate

Cat.No: T6549

Synonym: Isepamicine (Isepamycin,硫酸异帕米星,Isepamicin Sulphate,Isepacin,sch21420) Sulphate

Target: Antibacterial, Antibiotic

Clindamycin hydrochloride

Cat.No: T6448

Synonym: 盐酸克林霉素,Sobelin HCl,Cleocin,Clindamycin HCl,Clinimycin HCl

Target: Antibacterial, Antibiotic

Bisindolylmaleimide III

Cat.No: T77628

Target: PKC

Dihydrostreptomycin sulfate

Cat.No: T2211

Synonym: Dihydrostreptomycin sesquisulfate,双氢链霉索

Target: Antibacterial, Antibiotic

Cat.No: T50026

Target: HSV

Cat.No: T1767

Synonym: BMH21

Target: DNA/RNA Synthesis

Cat.No: T1747

Synonym: TR 700,特地唑胺,DA-7157,泰地唑利,Torezolid

Target: MAO, Antibacterial, Antibiotic

Cat.No: T3052

Synonym: Bonomycin,Norcycline,Sancyclinum,山环素,6-Demethyl-6-deoxytetracycline

Target: Antibacterial

Cat.No: T1569

Synonym: 替加环素,GAR-936

Target: ribosome, Antibacterial, Antibiotic, Autophagy

PF-06446846 hydrochloride

Cat.No: T16491

Target: Others

Cat.No: T16703

Synonym: CX-3543

Target: DNA/RNA Synthesis

Cat.No: T16567

Synonym: PQR-530

Target: PI3K, mTOR

Cat.No: T36675

Clindamycin hydrochloride monohydrate

Cat.No: T22297

Synonym: Clindamycin alcoholate

Target: Antibiotic

Cat.No: T10365

Target: Others

Formylmethionyl-alanyl-leucine

Cat.No: T31854

Synonym: Fmet-ala-leu

Cat.No: T25733

Cat.No: T69823

Cat.No: T11310

Target: Others

Cat.No: T24819

Synonym: U 19183,B 120121L19,B120121L19,U-19183,U19183

Cat.No: T71199

Cat.No: T35769

Capreomycin free base

Cat.No: T71449

Doxycycline fosfatex

Cat.No: T68614

Cat.No: T31616

Synonym: NB-124,NB 124,NB124,ELX02,ELX 02

Cat.No: T40998

Cat. No.	Product Name	Target	Signaling Pathways
T3836	Eudesmin	MAPK; S6 Kinase	MAPK; PI3K/Akt/mTOR signaling
	Eudesmin 通过抑制S6K1信号通路来干扰成脂分化，具有抗肿瘤、抗炎和抗菌活性。
T6S1302	Carnosol	Nrf2; Endogenous Metabolite; S6 Kinase	Immunology/Inflammation; MAPK; Metabolism; PI3K/Akt/mTOR signaling
	Carnosol 是 Nrf2激活剂，增加 Nrf2 的水平以及能促进血红素氧合酶 1（HMOX1）表达。它是核糖体 S6激酶(RSK2)抑制剂，可用于胃癌相关研究，IC50值约为 5.5 μM。
T0950	Neomycin sulfate Framycin sulfate,硫酸新霉素	Phospholipase; ribosome; Antibacterial; Antibiotic	Metabolism; Microbiology/Virology
	Neomycin sulfate (Framycin sulfate) 是一种广谱的氨基糖苷类抗生素。Neomycin sulfate 可以阻断细菌蛋白质的合成以发挥抗菌活性。Neomycin sulfate 常用于筛选具有 Neo 抗性基因的原核和真核细胞。
T0895	Oxytetracycline 土霉素,Terramycin	ribosome; Endogenous Metabolite; Antibacterial; Antibiotic; HSV	Metabolism; Microbiology/Virology
	Oxytetracycline (Terramycin) 是一种四环素类抗生素。它强力抑制革兰氏阴性和革兰氏阳性细菌。它是一种蛋白质合成抑制剂，可阻止 aminoacil-tRNA 与复杂的核糖体 RNA 结合，具有抗 HSV-1的活性。
T6624	Oxytetracycline Dihydrate 土霉素二水合物,地霉素,Terramycin Dihydrate	Others; Endogenous Metabolite; Antibacterial; Antibiotic; HSV	Metabolism; Microbiology/Virology; Others
	Oxytetracycline Dihydrate (Terramycin Dihydrate) 是一种四环素类抗生素，可抑制革兰氏阴性和革兰氏阳性细菌。它是一种蛋白质合成抑制剂，可阻止 aminoacil-tRNA 与复杂的核糖体 RNA 结合，还具有抗 HSV-1的活性。
T2871	Quercitrin Sophoretin,3-rhamnosyl quercetin,Quercetin 3-rhamnoside,Xanthaurine,槲皮苷,Meletin	Reactive Oxygen Species; S6 Kinase; Autophagy	Autophagy; Immunology/Inflammation; MAPK; Metabolism; NF-κB; PI3K/Akt/mTOR signaling
	Quercitrin (3-rhamnosyl quercetin) 是苦荞麦中的一种天然产物，具有抗炎作用，有用于心血管疾病的研究潜力。
T21430	Oxytetracycline Hydrochloride Biosolvomycin,盐酸土霉素,Oxytetracycline HCl,Oxytetracycline.HCl,Dalimycin,Oxytetracycline, Sodium Salt,Dalinmycin	Antiviral; Endogenous Metabolite; Antibacterial; HSV	Immunology/Inflammation; Metabolism; Microbiology/Virology
	Oxytetracycline Hydrochloride (Dalimycin) 是由 Streptomyces rimosus 生产的，一种具有抗菌活性的四环素衍生物。它干扰氨酰-tRNA 与 mRNA-核糖体复合物的结合，从而阻止肽延伸并抑制蛋白质合成。
T0335	Sodium salicylate 水杨酸钠,Salicylic acid sodium salt,2-Hydroxybenzoic acid sodium salt	Apoptosis; NF-κB; COX; S6 Kinase; Autophagy	Apoptosis; Autophagy; Immunology/Inflammation; MAPK; Neuroscience; NF-κB; PI3K/Akt/mTOR signaling
	Sodium salicylate (2-Hydroxybenzoic acid sodium salt) 是一种S6K 的抑制剂，可抑制COX-2活性。它还是一种NF-κB 抑制剂，可降低炎症基因的表达，促进老化肌肉的修复。
T1441	Capreomycin sulfate Capastat sulfate,硫酸卷曲霉素	ribosome; Antibacterial; Antibiotic	Microbiology/Virology
	Capreomycin sulfate (Capastat sulfate) 是一种多肽类抗生素，与其它抗生素结合用于MDR-肺结核。
T16552	Pleuromutilin Mutilin 14-glycolate,Drosophilin B,截短侧耳素	Antibacterial; Antibiotic	Microbiology/Virology
	Pleuromutilin (Drosophilin B) 通过与细菌的 50S 核糖体亚基结合来抑制细菌蛋白质的合成。
T16674	Pseudouridine	Endogenous Metabolite	Metabolism
	Pseudouridine 是非编码 RNA 中丰富的修饰核苷，通过稳定 RNA 结构增强核糖体 RNA 和的转移 RNA 功能。
T1313	Nitrofurantoin Furadantine,呋喃妥因,Macrodantin,Furadonine	Antibacterial; Antibiotic	Microbiology/Virology
	Nitrofurantoin (Furadantine) 是一种具有口服活性的广谱内酰胺酶抗菌剂。它是一种抗生素，可研究尿路感染。
T1304	Chlortetracycline hydrochloride Isphamycin,Chlortetracycline HCl,7-Chlorotetracycline hydrochloride,盐酸金霉素	ribosome; Antibacterial; Antibiotic	Microbiology/Virology
	Chlortetracycline hydrochloride (Isphamycin) 是一种特异性钙离子载体抗生素, 抑制氨酰 tRNA 结合到核糖体。
T11233	Erythromycin thiocyanate	Antibacterial	Microbiology/Virology
	Erythromycin thiocyanate acts by binding to bacterial 50S ribosomal subunits and inhibits RNA-dependent protein synthesis by blockage of transpeptidation and/or translocation reactions, without affecting synthesis of nucleic acid .Erythromycin thiocyanate
T62625	11-O-Methylpseurotin A
	11-O-Methylpseurotin A为一种(PKS/NRPS)混合聚酮合成酶-非核糖体肽合成酶化合物，其特性为选择性抑制Hof1缺失菌株。
T16896	SL 0101-1 SL0101	S6 Kinase	MAPK; PI3K/Akt/mTOR signaling
	SL 0101-1 (SL0101) 是一种可透过细胞膜且具有选择性、高效性、可逆性、ATP竞争性的 p90核糖体S6激酶(RSK) 的抑制剂，对 RSK 的 IC50 值为 89 nM。SL 0101-1 (SL0101) 也是一种有效的 RSK1/2 抑制剂，其 Ki 值为 1 μM。

天然产物

Cat.No: T3836

Target: MAPK, S6 Kinase

Cat.No: T6S1302

Target: Nrf2, Endogenous Metabolite, S6 Kinase

Neomycin sulfate

Cat.No: T0950

Synonym: Framycin sulfate,硫酸新霉素

Target: Phospholipase, ribosome, Antibacterial, Antibiotic

Oxytetracycline

Cat.No: T0895

Synonym: 土霉素,Terramycin

Target: ribosome, Endogenous Metabolite, Antibacterial, Antibiotic, HSV

Oxytetracycline Dihydrate

Cat.No: T6624

Synonym: 土霉素二水合物,地霉素,Terramycin Dihydrate

Target: Others, Endogenous Metabolite, Antibacterial, Antibiotic, HSV

Cat.No: T2871

Synonym: Sophoretin,3-rhamnosyl quercetin,Quercetin 3-rhamnoside,Xanthaurine,槲皮苷,Meletin

Target: Reactive Oxygen Species, S6 Kinase, Autophagy

Oxytetracycline Hydrochloride

Cat.No: T21430

Synonym: Biosolvomycin,盐酸土霉素,Oxytetracycline HCl,Oxytetracycline.HCl,Dalimycin,Oxytetracycline, Sodium Salt,Dalinmycin

Target: Antiviral, Endogenous Metabolite, Antibacterial, HSV

Sodium salicylate

Cat.No: T0335

Synonym: 水杨酸钠,Salicylic acid sodium salt,2-Hydroxybenzoic acid sodium salt

Target: Apoptosis, NF-κB, COX, S6 Kinase, Autophagy

Capreomycin sulfate

Cat.No: T1441

Synonym: Capastat sulfate,硫酸卷曲霉素

Target: ribosome, Antibacterial, Antibiotic

Cat.No: T16552

Synonym: Mutilin 14-glycolate,Drosophilin B,截短侧耳素

Target: Antibacterial, Antibiotic

Cat.No: T16674

Target: Endogenous Metabolite

Cat.No: T1313

Synonym: Furadantine,呋喃妥因,Macrodantin,Furadonine

Target: Antibacterial, Antibiotic

Chlortetracycline hydrochloride

Cat.No: T1304

Synonym: Isphamycin,Chlortetracycline HCl,7-Chlorotetracycline hydrochloride,盐酸金霉素

Target: ribosome, Antibacterial, Antibiotic

Erythromycin thiocyanate

Cat.No: T11233

Target: Antibacterial

11-O-Methylpseurotin A

Cat.No: T62625

Cat.No: T16896

Synonym: SL0101

Target: S6 Kinase

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