SB-203580 (Adezmapimod) is a p38 MAPK inhibitor with IC50 of 0.3-0.5 μM.

SB-202190 is a highly selective, potent and cell-permeable inhibitor of p38 MAP kinase with IC50 values of 50 nM and 100 nM for p38α and p38β respectively; also shows slightly weaker activity for BRD4 (Kd=3.4 μM).

SB-216763是一种高效、选择性和ATP竞争性的GSK-3抑制剂，对GSK-3α和GSK-3β的IC50均为34.3 nM。

IWR-1是一种抑制Wnt/β-连环蛋白信号通路的tankyrase抑制剂。

KY02111 can inhibit Wnt signaling and promote differentiation of hPSCs to cardiomyocytes.

LY364947（HTS466284）是一种有效的ATP竞争性TGFβR-I抑制剂，IC50值为59 nM，并对TGFβR-II具有7倍的选择性。

IQ-1 enables Wnt/β-catenin-driven expansion of mouse ESCs and prevents spontaneous differentiation, Maintains embryonic stem cell (ESC) pluripotency in Wnt3a-treated cells and prevents PP2A/Nkd interaction.

Laduviglusib (CHIR-99021)是一种有效、选择性且具有口服活性的 GSK-3α/β 抑制剂，可用作细胞疗法中的辅助试剂。

Shz-1 is an enhancer of myocardial regenerative repair by stem cells that specifically activates Nkx2.5.

Reversine, a synthetic purine analogue(2,6-disubstituted purine), is a potent human A3 adenosine receptor antagonist with Ki of 0.66 μM, and a pan-aurora A/B/C kinase inhibitor with IC50 of 12 nM/13 nM/20 nM, respectively.

ISX-9 is a small molecule inducer of adult neural stem cell differentiation.

Dorsomorphin 是一种选择性、ATP 竞争性的 AMPK 抑制剂 (在没有 AMP 的情况下，Ki 为 109 nM)，选择性抑制 BMP I 型受体 ALK2、ALK3 和 ALK6，并可逆转 Urolithin A导致的自噬激活和抗炎作用。

LW6是一种 HIF-1α 抑制剂，具有降低 HIF-1α 蛋白表达的能力，在癌症和缺氧相关疾病研究中具有重要应用。

Retinoic acid (Vitamin A acid)作为 RAR 核受体的激动剂，用于细胞疗法中的辅助试剂。

Zebularine is a DNA methylation inhibitor which forms a covalent complex with DNA methyltransferases, it also inhibits cytidinedeaminase with Ki of 2 μM.

(-)-Epigallocatechin Gallate 是绿茶中的主要多酚，能抑制细胞增殖并诱导细胞凋亡，抑制谷氨酸脱氢酶 1/2 (GDH1/2, GLUD1/2) 活性，具有抗癌、抗氧化和抗炎特性。

CAY10585(LW6 , HIF-1α 抑制剂) 是一种新型 HIF-1 抑制剂，IC50 为 4.4 μM，能降低 HIF-1α 蛋白表达而不影响 HIF-1β 表达。